The brain is one of the main targets of gonadal steroid hormones. In addition, it contains many of the steroid metabolizing enzymes. The effect of gonadal steroids on brain development and maturation has been well documented [1,2]. The vast literature on the subject has introduced the common belief that gonadal steroids may be the only effectors of the brain sexual differentiation, overshadowing other key elements. Although there is no doubt about its importance, the dogma of the gonadal origin of somatic differentiation, including neuronal cells, usually implies that XX and XY cells, accordingly stem cells, are functionally equivalent unless gonadal secretions act on them in a sex-specific manner. The human Y chromosome encodes 27 different proteins  eight of which are expressed in the male brain and could have a male-specific effect on the brain, independent of any gonadal hormone influence [4,5]. Furthermore, XX cells contain an X chromosome that received a paternal genomic imprint, whereas XY cells do not, a fact that is likely to contribute to autonomous differences between male and female cells. De Vries and colleagues  generated mice in which the testis-determining gene
The chapter will first discuss the potential of stem cells for brain repair, tissue regeneration and function recovery, second the effect of sex on stem cell fate whether neural stem cells or peripheral stem cells, and third the potential translation in clinics. The goal of the present proposal is to discuss the therapeutic relevance of the largely under-explored sex- and age-based differences in the capacity of NSC to engage in neurogenesis programming. Indeed, beyond understanding the physiology and biochemistry of aging NSC, for both sexes, the overall objective is to discuss the potential foundation for future studies aimed at tailoring NSC transplantation strategies for brain repair as a function of sex/age, as well as considering sex- and age-specific pharmacological approaches towards the development of neurogenesis-inducing treatments.
2. Stem cells — Hope and hurdles
If one had to explain the excitement and exhilaration stem cell therapy triggers in the field of tissue repair and the hope it represents, a comparison that would make sense is the new horizons opened after the first man in flight or the first man in space. The hopes and hypes reflect the potential offered by stem cell therapy and in that sense, they are completely justifiable. Probing PubMed with ‘stem cell’ and ‘therapy’ as keywords in certainly the best way to understand how the interest of research community significantly evolved over 40 years. Indeed, in 1970, only 13 publications related to stem cell therapy were referenced in PubMed, compared to 7942 in 2010 (Figure 1). A slightly restricted search for ‘stem cell’, ‘therapy’ and ‘brain’ reveals that the number of publications related to brain repair, although increasing, is “plateauing” at 10% of the total number of publications focused on stem cell therapy for the past five years (Figure 1). This status reflects a greater difficulty to generate clear data on experimental and clinical stem cell therapy for brain repair than with any other organs. This situation is likely due to the unique architectonic of the brain, the way it interfaces with the peripheral compartment and the seemingly endless cell phenotypes that compose the brain.
It is remarkable that the first report using the words ‘neural stem cells’ was published not that long ago in 1992, reaching the hundred only in 2001, catching up in 2010 with 714 references with the number of publications that include ‘stem cell’, ‘therapy’ and ‘brain’ (Figure 1). Although one cannot deny that the amount of data degenerated nowadays on NSC and brain repair is getting more important, the rather slow pace at which progresses are still reported does not prefigure any substantial impact in clinics to be made in the near future. Many hurdles lie on the road of brain stem cell therapy. The first one, and not necessarily by order of importance, is directly related to the various types of stem cells considered as a potential source for brain transplantation. Human embryonic stem cells (hESC) [16,17], fetal NSC [18,19], post-natal or adult NSC [20-25], induced pluripotent stem cells (iPS) [26-29], bone marrow stem cells (BMSC) [30-36], mesenchymal stem cells (MSC) [37,38], umbilical cord blood-derived stem cells [39-41] and adipose tissue-derived stem cells [42,43]. This luxury of choice turned out to become an increasingly difficult situation to handle, generating at best a non-consensual agreement as to which stem cell type should be used for what type of neurological disorder. Overall, it seems that potential stem cell sources have been insufficiently characterized, impeding clinical translation. Although it sounds like a very easy statement to make, we have to admit that our knowledge in long-term outcome of stem cell transplantation in the brain is extremely limited. In example, grafting stem cells not from neurodermal origin in an attempt to replace degenerated neurons supposes a transdifferentiation mechanism of the transplanted stem cells prior to undergo successful differentiation in the appropriate neuronal phenotype [44-49]. Very little literature is currently available in transdifferentiation mechanisms and even more so, recent data reported that transdifferentiation is reversible and may be restricted to certain type of stem cells [48,49], raising the question of what would happen in vivo. A major concern is the development of gliomas or other brain cancer types secondary to stem cell transplantation. Indeed, the property of stem cells to self-renew is exactly what confer them the capacity of being highly tumorigenic [50-53]. It is particularly true for the hESC which tumorigenic properties have been extensively studied . In addition, iPS have been developed to exactly mimic embryonic stem cells neurogenic capacity without having the capacity to induce brain tumor formation. However, the iPS safety is still being debated . A clinical case has been reported very recently regarding a young boy who developed glioneuronal neoplasm four years after having received allogenic hESC transplantation in an attempt to improve his ataxia telangiectasia symptomatology . It is remarkable that the tumor cells were identified as deriving from at least two of the donors composing the hESC pool from which the young boy received multiple transplantations. This specific data points out the possibility that using pool of donors may increase the risk of developing tumor or even host-versus-graft reaction [54-57]. Beyond the trivial concern of stem cells tumorigenesis remains the question of inducing the proper neural phenotype needed to replace a specific type of neuron. Parkinson’s disease is without any doubt the neurodegenerative disease for which brain transplant has been studied the most extensively. A consensual strategy seems to pre-differentiate the stem cells toward the dopaminergic fate prior to conduct the transplantation [58,59] and as a consequence, many studies have been conducted to develop suitable protocols [58-62]. The same question arises to ensure that stem would undergo GABAergic differentiation prior to be used in patients suffering from Huntington’s disease . However, despite many efforts to establish validated differentiation protocols, the phenotypic fate followed by transplanted stem cells still remain largely uncontrolled [64-66] and likely involves stem cells intrinsic properties, i.e. region or context dependency, sex or age [14,67-70]. In a medical context of growing interest for global personalized medicine in general  and focused on regenerative medicine in particular [27,72-74], answering the question “What stem cell for whom?” never appeared as critical.
3. Stem cells transplantation in clinics — From hype to disillusion, keeping the faith alive
The main reason of the arisen interest for stem cell therapy in central and peripheral nervous system lies in the fact that it addresses neuropathologies and conditions for which neurological damages are extensive, socially debilitating and irreversible and for which there is no ‘magic pill’. Stem cell therapy for tissue repair is generating very high expectation to treat neurodegenerative diseases like Parkinson’s disease [66,75], amyotrophic lateral sclerosis [76-81], Huntington’s disease [18,19,82-84], Alzheimer’s disease [85-87], multiple sclerosis [88-90], spinal cord injury [91,92] and retina degeneration [26,31,93]. Clinical translation has been, up to now and by far, most exclusively conducted in patients suffering from Parkinson’s, Huntington’s disease or amyotrophic lateral sclerosis and, to our knowledge, there is no data reported clinical evaluation of stem cell transplantation in Alzheimer’s disease or retina degeneration.
3.1. Parkinson’s disease
Two groups actively involved in conducting clinical studies assessing the therapeutic effectiveness of stem cell transplantation to treat Parkinson’s disease reported conflicting results [94-97]. In a first study, six Parkinson patients were to received bilateral transplantation of fetal nigral tissue the post-commissural putamen . The fetal material was obtained from the mesencephalon of legally aborted fetus and used as solid grafts. Each patient received tissue pooled from 3 to 4 fetuses. Two years outcome measurement showed an improvement of the Unified Parkinson’s Disease Rating Scale (UPDRS), and an increase of [18F]-fluorodopa uptake in the putamen. On the downside, all patients started experience dyskinesia few weeks after the transplantation. When the same group performed the same type of study on a much larger cohort, the outcome was much more deceiving . Out of the 34 patients followed up to 2 years, none of them displayed clinically relevant improvement although post-mortem analysis showed a robust survival of grafted dopaminergic neurons. These results led the authors to conclude that fetal nigral transplantation could not constitute a therapy for Parkinson’s disease. One can argue that using solid grafts rather than well characterized stem cell/neuroblast primary culture might have impaired the capacity of newly formed neurons to establish connections with the pre-existing network. This point is extensively discussed in a very recent review . A more striking issue to us is the lack of information related to the sex of the donor suggesting that the tissue samples were pooled and grafted regardless of a potential sex-based difference in stem cell biology which could have an impact on the clinical outcome. In an other study, 40 patients were bilaterally grafted in the putamen with a mixture of stem cells/dopaminergic neuroblasts obtained from cultured mesencephalic tissue from 4 embryos . Follow-up at one year post-transplantation showed some benefit but only for the patients 60 years of age or younger. In addition, the benefit was clinically significant only in some areas of the UPDRS and 15 percent of the patients became dyskinetic. A post-analysis of the one-year follow-up data revealed a sex-based difference in the graft outcome . Indeed, the male patients displayed more clinical benefit than the female patients after the first year but the progress rate increased in the female to catch up with the male at the end of the second year of follow-up . In addition, a follow-up performed over 4 years on 33 patients out of the 40 initially included showed that the age-based difference observed earlier  disappeared as the oldest patients’ overall UPDRS was catching-up over the 4-years period of time on the youngest’ one . The authors concluded that some clinical benefit was still clearly present 4 years after transplantation with however no correlation with the [18F]-fluorodopa uptake. Although the measured outcome seemed to be more encouraging than in the first series of experiments, the cell preparation may account for it, the results remain rather inconsistent and deceiving. On the same line, earlier clinical studies reported a somewhat beneficial effect of fetal mesencephalic neurons in patients affected by Parkinson’s disease [75,98,99]. Several reasons have been proposed such inconsistency, among which the number of cells, the grafting site, the preparation of the cells, the use of immunosuppressant or the lack of functional rehabilitation associated with the transplantation [66,100] but no consensus has been reached so far. In addition, a recurrent issue that clinicians and patients are facing is the graft-induced dyskinesia. This locomotor alteration is a direct consequence of the transplantation and its causes and possible solutions remain rather elusive  and is seen as a permanent drawback to any progress made in stem cell transplantation to treat Parkinson’s disease. As mentioned earlier, it is quite interesting that the cells of several donors were pooled with no reference to their sex as a factor of graft outcome. It is even more surprising since a sexual dimorphism with functional implications has been established for human muscle stem cells [9,12,13] and monkeys mesenchymal stem cells .
3.2. Amyotrophic lateral sclerosis
Amyotrophic lateral sclerosis (ALS) is a late-onset neurodegenerative disease that selectively affects motor neurons in the cortex, brain stem and spinal cord  for which there is no treatment. Several clinical studies have been conducted which results raised some optimism but, overall, data related to the transplantation outcome remain, as with Parkinson’s disease, contradictory and inconsistent. A very recent report based on thirteen clinical cases demonstrated the feasibility and the therapeutic relevance of performing autologous bone marrow-derived hematopoietic cell transplantation in patients displaying severe sporadic ALS . One year after receiving CD34+ cells transplantation in the brain stem and the beginning of the spinal cord, most of the patients displayed an improvement of their status. The majority of the patients regained neuronal stimulatory capacity of their muscle, as measured by post-operative electroneuromyogram, and a better bulbar score. Some of them even recovered walking capacity compatible with a daily life. However, the majority of the patients who experienced a post-operative gain of function started to see their clinical status decline at one-year follow-up. This piece of data, rather than suggesting that bone marrow-derived stem cells cannot be used as a therapeutic tool suggests instead that the transplantation procedure should be repeated in order to obtain maximum functional recovery. An other study demonstrated the beneficial effect of stem transplantation as a cytotherapeutic tool for ALS. Thirty-three patients diagnosed with severe sporadic ALS were to receive autologous transplantation of peripheral blood mononuclear cells (PBMC) in the motor cortex and followed-up over one year . All the patients that received CD133+ PBMC transplantation experienced a dramatic improvement of their clinical status as measured by the ALS Functional Rating Scale-Revised. The most striking beneficial effect resulting from the transplantation was the increase in the median survival from 19 months for the patients in the sham group to 66 months in the treated group. More remarkably, the patients’ quality of life was also dramatically improved. Indeed, in the sham group, half of the patients had to undergo tracheotomy and gastrostomy at 12-months follow-up compared to the no tracheotomy and only one gastrostomy performed in the group of patients who received PBMC transplantation. Taken together, these results show promises for ALS cytotherapy. However, some more recent clinical studies reported that transplanting stem cells in ALS patients did not result in any beneficial effect [79,81]. In the first case, patients received autologous transplantation of mesenchymal stem cells isolated from bone marrow in the spinal cord at T4-T5 and T5-T6 level and were followed-up for 24 months . Although MRI imaging ascertained graft survival, clinicians did not observe any clinical improvement. However, it is noteworthy that the patients recruited for this study were diagnosed with mild to moderate sporadic ALS unlike the two previous studies described above for which the patients were diagnosed with severe sporadic ALS. This apparent discrepancy may indicate that the stage of the disease at which the stem cell transplantation is to be performed has to be cautiously defined as it may critically affect the clinical outcome. In the second case, patients from 3 different centers received stem cells transplantation and were then evaluated at 12-months post-transplantation . This study is difficult to interpret as it includes a total of 12 patients who received 3 different types of stem cells, depending on the clinical center of origin, and using intratechal route, intravenous or both. The stem cells used were embryonic olfactory ensheating stem cells, mesenchymal stem cells or CD34+ stem cells without further explanation as to how many embryos were used per patients or if the graft of adult stem cells was autologous or not. However, a common point shared with the previous reported study, beside its lack of success at restoring the patients’ motor function, is the fact that most of the patients recruited were diagnosed with a mild to moderate sporadic ALS supporting the idea 1) that mild to moderate stage of ALS might not be the best moment to start stem cell therapy, or that 2) the types of stem cells that were proven to be therapeutically relevant in the severe cases might not be as relevant to treat mild or moderate cases of ALS. These results certainly advocate for a better personalized therapy to the patient.
3.3. Huntington’s disease
Huntington’s disease is a neurodegenerative condition which is clinically characterized by cognitive, motor and psychiatric deterioration and leads in 20 years maximum to the death of the patient. There is currently no treatment for this disease and stem cell therapy is being extensively investigated as a therapeutic tool. Many attempts of restoring some or all the lost functions by stem cells transplantation have been made but the long term results have been so far deceiving. Motor and cognitive functions improvement has been reported in some patients 1 year after the transplantation  but these improvements plateaued at 2 years and to finally completely reverse at 4-6 years . Other studies reported successful engraftment and neuronal differentiation  associated with an improved cortical metabolism  unfortunately not accompanied by any clinical improvement. A major finding that is commonly reported on long-term post-mortem histological study is the poor survival of the transplanted stem cells [83,84] which is believed to be due to a reaction of the host immune system against the grafted cells [54,84]. Interestingly, to our knowledge, all the clinical studies conducted on Huntington patients reported having used human embryonic stem cells [18,19,54,82-84,102] which is a quite surprising situation if we compare to the variety of stem cell types used in Parkinson’s disease and ALS. In addition, one is force to at least acknowledge the fact that the stem cells used are from embryonic origin may be the factor that triggers the immune response. Indeed, human embryonic stem cells are not devoid of immunogenicity and are capable of triggering a significant immune response leading to graft rejection [54,103]. In regard of what has been accomplished in Parkinson’s disease and ALS, autologous transplantation of PBMC or bone marrow-derived stem cells seems to be more appropriate and one may wonder why it has not been tried yet. An other point that raises question is the fact that all the studies reported, except one , transplanted human embryonic stem cells pooled from several embryos, neither mentioning how many embryos were used per patient nor the sex of the embryos.
3.4. Other indications for stem cell therapy
Stem cell therapy, beyond the controversy of using embryonic stem cells, is a very seducing and highly promising therapeutic strategy for repairing the central nervous system. Using stem cell transplantation has become a very appealing topic for many researchers and clinicians around the world. However, developing and implementing such protocols to other neurological conditions than the ones discussed above reveals to be an even more challenging endeavor. Among the neurodegenerative disease that would benefit from stem cell therapy, Alzheimer’s disease evidently represents a major interest. Probably because of the complexity of the disease and our very limited knowledge about it, stem cell therapy for Alzheimer’s disease is still in a preclinical stage [85-87]. Stem cell therapy for spinal cord injury is certainly at the forefront of the preclinical research in order to establish valid therapeutic protocols to be translated in clinics, but once again translating the knowledge acquired in animal models facing several hurdles, among which cytotherapy specificity and safety [29,87,91,92,104,105]. Brain stroke is a neurological condition that could require extensive tissue reconstruction and results obtained in animal models are very encouraging [20,24,106]. So far, only one clinical study has been conducted in five patients by autologous transplantation of bone marrow-derived stem cells . One year follow-up showed good safety profile and a trend to clinical improvement. Retina degeneration, whether idiopathic or post-traumatic, is a major problem as it is irreversible, without treatment and leads to blindness in most of the case. However, the retina architectonic and the differentiation process of retina stem cell represent two main problems to clinical translation. Indeed, many in vivo and in vitro studies have been conducted in various laboratories [26,30-32,35,37,45,107-117] showing promising results. However, although the post-transplantation cell survival was excellent in all cases, the retina structure revealed itself to be an obstacle to stem cell migration. In addition, the differentiation process that leads to the formation of mature retina cell is by far more complex than in the brain.
4. Looking at the forest instead of the tree — Turning the tide on clinical setbacks
We have recently published in a recent report that the estrogen receptor ERα is differentially expressed in male and female NSC. NSC isolated from 3 month-old rats display sexual dimorphism in the expression of estrogen receptor alpha and beta . Male NSC contain one third of the ERα levels, whereas ERβ levels were 3 times greater than those expressed NSC isolated from same age females. Moreover, our data demonstrated that the ERα/ERβ ratio was close to 1 in the male but 10 fold higher in the female NSC. Interestingly, others previously reported that the expression of steroid receptors in the fish inner ear varies between sexes . Such sexual dimorphism has been previously described in mature neurons of various brain structures [119,120] and has been shown to have a role in the differentiation of sexual behavior and gender identity . Indeed, ERα has been shown to be primarily involved in masculinization, whereas ERβ is primarily involved in defeminization [122,123]. From birth and throughout life, sex hormones physiology and homeostasis are different between men and women which suggest that transplanting the “inadequate” type of NSC to the patient may not lead to the expected beneficial effect. Indeed, consequences in clinics may run from a lack of recovery to partial or inadequate recovery. Dissimilarity between NSC and the recipient tissue may cause these undesirable effects. Interestingly, in the same manner, NSCs isolated from 20 month old male and female rats displayed a dramatic increase in ERα and ERβ expression that was equivalent in both sexes, suggesting that male and female NSCs are not equal before aging. The effect of estrogens on neurogenesis has been extensively studied and it is commonly agreed that estrogens simultaneously promote NSC proliferation and differentiation [124-129]. There is increasing evidence on the estrogenic aspect of neurogenesis; however, the differential roles of ERα and ERβ in this process still remain to be fully characterized. Considering the currently known role of estrogens in NSC physiology and the regulation of the neurogenesis [124,126,128-132], the sexual dimorphism we observed in ERα and ERβ expression between male and female NSC  supports a sex-based intrinsic difference in the regulation of neurogenesis. In addition, ERα genotype has been recently reported to be responsible for the inter-individual variability of responses to estrogen and testosterone in mesenchymal stem cell-derived osteoblasts . Moreover, estradiol has been described to alter neurogenesis in female, but not male rats . We also provided evidence that male NSC expressed a dramatically higher level of CYP19 than female NSC  which supports a capacity for male NSC, unlike female NSC, to metabolize testosterone and in turn, to produce estradiol. Such biochemical sexual dimorphism may underlie a steroid-related pharmacological counterpart as male NSC may therefore have the ability to alter their local environment and modulate endogenous neurogenesis in a different manner than female NSC may do. Remarkably, an autocrine control loop in two different systems, the NSC kinin/kallicrein pathway  and the androgenic apparatus of human bone marrow stromal cells . It is noteworthy that the sex-based differences unveiled in vitro translated in vivo as we recently reported . Indeed, the outcome of NSC transplantation in brain was shown to tightly depend on the sex of the donor and the sex of the recipient. Interestingly, in some cases cross-sex grafting provided better cell survival results than same-sex transplantation. As others also demonstrated the occurrence of a sexual dimorphism in the neurogenic capacity of rhesus monkeys mesenchymal stem cells , we are the first to have shown a direct impact on the outcome of stem cell transplantation . Nevertheless, stem cell sexual dimorphism has been previously demonstrated by others in various organs [9,12,13,67,134] and organisms , and it is our opinion that sex should be considered as a critical factor and integrated in the development of future clinical protocol.
There is a consensual agreement that age-associated alterations in the brain play an important role in the decline of neurogenesis reported in aging [11,139-141]. However, very little work has been done in defining the age-related alteration of NSC neurogenic properties. Old mice have been shown to have less NSC in the subventricular zone (SVZ) compared to young ones, and a similar reduction has been reported in the number of NSC maintained as neurospheres and recovered in culture
Stem cell therapy holds a lot of promises for brain repair and the recovery of impaired neurological functions. However, despite the generation of a large amount of encouraging results produced on various animal models, the translation at the patient’s bed seems to be delayed. Facing mitigated results from the few clinical studies that have been conducted so far, we are constrained to a cautious optimism. Indeed, the low success rate encountered in clinics questions our knowledge on the topic and suggests that we go back to a more fundamental bench work. Indeed, the high number of stem cell types, to which have to be added the various engineering counterparts, turn a luxury of choice into a situation where it is extremely, if not impossible, to determine what cell type or cell line would be the best candidate for tissue repair. Compelling evidence suggests that sex may be a critical determining factor of stem cell transplantation outcome in the brain. Surprisingly, none of the clinical studies reported to date took this parameter into consideration. Furthermore, we foresee that NSC differentiation induced by neurogenic agents
Phoenix CH, Goy RW, GERALL AA, Young WC. Organizing action of prenatally administered testosterone propionate on the tissues mediating mating behavior in the female guinea pig Endocrinology 1959; 65: 369-382.
Smith ER, Davidson JM. Differential responses to hypothalamic testosterone in relation to male puberty Am J Physiol 1967; 212: 1385-1390.
Skaletsky H, Kuroda-Kawaguchi T, Minx PJ, Cordum HS, Hillier L, Brown LG, Repping S, Pyntikova T, Ali J, Bieri T, Chinwalla A, Delehaunty A, Delehaunty K, Du H, Fewell G, Fulton L, Fulton R, Graves T, Hou SF, Latrielle P, Leonard S, Mardis E, Maupin R, McPherson J, Miner T, Nash W, Nguyen C, Ozersky P, Pepin K, Rock S, Rohlfing T, Scott K, Schultz B, Strong C, Tin-Wollam A, Yang SP, Waterston RH, Wilson RK, Rozen S, Page DC. The male-specific region of the human Y chromosome is a mosaic of discrete sequence classes Nature 2003; 423: 825-837.
Maxson SC. Searching for candidate genes with effects on an agonistic behavior, offense, in mice Behav Genet 1996; 26: 471-476.
Xu J, Burgoyne PS, Arnold AP. Sex differences in sex chromosome gene expression in mouse brain Hum Mol Genet 2002; 11: 1409-1419.
De Vries GJ, Rissman EF, Simerly RB, Yang LY, Scordalakes EM, Auger CJ, Swain A, Lovell-Badge R, Burgoyne PS, Arnold AP. A model system for study of sex chromosome effects on sexually dimorphic neural and behavioral traits J Neurosci 2002; 22: 9005-9014.
Herrmann JL, Abarbanell AM, Weil BR, Manukyan MC, Poynter JA, Wang Y, Coffey AC, Meldrum DR. Gender dimorphisms in progenitor and stem cell function in cardiovascular disease J Cardiovasc Transl Res 2010; 3: 103-113.
Li WW, Penderis J, Zhao C, Schumacher M, Franklin RJ. Females remyelinate more efficiently than males following demyelination in the aged but not young adult CNS Exp Neurol 2006; 202: 250-254.
Matsumoto T, Kubo S, Meszaros LB, Corsi KA, Cooper GM, Li G, Usas A, Osawa A, Fu FH, Huard J. The influence of sex on the chondrogenic potential of muscle-derived stem cells: implications for cartilage regeneration and repair Arthritis Rheum 2008; 58: 3809-3819.
Payne KA, Didiano DM, Chu CR. Donor sex and age influence the chondrogenic potential of human femoral bone marrow stem cells Osteoarthritis Cartilage 2010; 18: 705-713.
Yuan J, Yu JX, Ge J. Sexual dimorphism on the neurogenic potential of rhesus monkeys mesenchymal stem cells Biochem Biophys Res Commun 2010; 396: 394-400.
Deasy BM, Lu A, Tebbets JC, Feduska JM, Schugar RC, Pollett JB, Sun B, Urish KL, Gharaibeh BM, Cao B, Rubin RT, Huard J. A role for cell sex in stem cell-mediated skeletal muscle regeneration: female cells have higher muscle regeneration efficiency J Cell Biol 2007; 177: 73-86.
Deasy BM, Schugar RC, Huard J. Sex differences in muscle-derived stem cells and skeletal muscle Crit Rev Eukaryot Gene Expr 2008; 18: 173-188.
Waldron J, McCourty AM, Lecanu L. Aging differentially affects male and female neural stem cell neurogenic properties Stem Cells Cloning Adv Appl 2010; 3: 119-127.
Waldron J, McCourty AM, Lecanu L. Neural stem cell sex dimorphism in aromatase (CYP19) expression: a basis for differential neural fate. Stem Cells Cloning Adv Appl 2011; 3: 175-182.
Cohen MA, Itsykson P, Reubinoff BE. Neural differentiation of human ES cells Curr Protoc Cell Biol 2007; Chapter 23: Unit.
Joannides AJ, Chandran S. Human embryonic stem cells: an experimental and therapeutic resource for neurological disease J Neurol Sci 2008; 265: 84-88.
Bachoud-Levi AC, Gaura V, Brugieres P, Lefaucheur JP, Boisse MF, Maison P, Baudic S, Ribeiro MJ, Bourdet C, Remy P, Cesaro P, Hantraye P, Peschanski M. Effect of fetal neural transplants in patients with Huntington's disease 6 years after surgery: a long-term follow-up study Lancet Neurol 2006; 5: 303-309.
Capetian P, Knoth R, Maciaczyk J, Pantazis G, Ditter M, Bokla L, Landwehrmeyer GB, Volk B, Nikkhah G. Histological findings on fetal striatal grafts in a Huntington's disease patient early after transplantation Neuroscience 2009; 160: 661-675.
Andres RH, Horie N, Slikker W, Keren-Gill H, Zhan K, Sun G, Manley NC, Pereira MP, Sheikh LA, McMillan EL, Schaar BT, Svendsen CN, Bliss TM, Steinberg GK. Human neural stem cells enhance structural plasticity and axonal transport in the ischaemic brain Brain 2011; 134: 1777-1789.
Einstein O, Friedman-Levi Y, Grigoriadis N, Ben-Hur T. Transplanted neural precursors enhance host brain-derived myelin regeneration J Neurosci 2009; 29: 15694-15702.
Ho AL, Keshavarzi S, Levy ML. Exploitation of genetically modified neural stem cells for neurological disease Adv Exp Med Biol 2010; 671: 74-92.
Koch P, Kokaia Z, Lindvall O, Brustle O. Emerging concepts in neural stem cell research: autologous repair and cell-based disease modelling Lancet Neurol 2009; 8: 819-829.
Lee IS, Jung K, Kim M, Park KI. Neural stem cells: properties and therapeutic potentials for hypoxic-ischemic brain injury in newborn infants Pediatr Int 2010; 52: 855-865.
Mack GS. ReNeuron and StemCells get green light for neural stem cell trials Nat Biotechnol 2011; 29: 95-97.
Carr AJ, Vugler AA, Hikita ST, Lawrence JM, Gias C, Chen LL, Buchholz DE, Ahmado A, Semo M, Smart MJ, Hasan S, da CL, Johnson LV, Clegg DO, Coffey PJ. Protective effects of human iPS-derived retinal pigment epithelium cell transplantation in the retinal dystrophic rat PLoS One 2009; 4: e8152.
Chen LW, Kuang F, Wei LC, Ding YX, Yung KK, Chan YS. Potential application of induced pluripotent stem cells in cell replacement therapy for Parkinson's disease CNS Neurol Disord Drug Targets 2011; 10: 449-458.
Okano H. Strategies toward CNS-regeneration using induced pluripotent stem cells Genome Inform 2009; 23: 217-220.
Tsuji O, Miura K, Okada Y, Fujiyoshi K, Mukaino M, Nagoshi N, Kitamura K, Kumagai G, Nishino M, Tomisato S, Higashi H, Nagai T, Katoh H, Kohda K, Matsuzaki Y, Yuzaki M, Ikeda E, Toyama Y, Nakamura M, Yamanaka S, Okano H. Therapeutic potential of appropriately evaluated safe-induced pluripotent stem cells for spinal cord injury Proc Natl Acad Sci U S A 2010; 107: 12704-12709.
Arnhold S, Absenger Y, Klein H, Addicks K, Schraermeyer U. Transplantation of bone marrow-derived mesenchymal stem cells rescue photoreceptor cells in the dystrophic retina of the rhodopsin knockout mouse Graefes Arch Clin Exp Ophthalmol 2007; 245: 414-422.
Inoue Y, Iriyama A, Ueno S, Takahashi H, Kondo M, Tamaki Y, Araie M, Yanagi Y. Subretinal transplantation of bone marrow mesenchymal stem cells delays retinal degeneration in the RCS rat model of retinal degeneration Exp Eye Res 2007; 85: 234-241.
Kociok N. Can the injection of the patient's own bone marrow-derived stem cells preserve cone vision in retinitis pigmentosa and other diseases of the eye? Graefes Arch Clin Exp Ophthalmol 2005; 243: 187-188.
Lu B, Wang S, Girman S, McGill T, Ragaglia V, Lund R. Human adult bone marrow-derived somatic cells rescue vision in a rodent model of retinal degeneration Exp Eye Res 2010; 91: 449-455.
Matsuse D, Kitada M, Ogura F, Wakao S, Kohama M, Kira JI, Tabata Y, Dezawa M. Combined Transplantation of Bone Marrow Stromal Cell-Derived Neural Progenitor Cells with a Collagen Sponge and Basic Fibroblast Growth Factor Releasing Microspheres Enhances Recovery After Cerebral Ischemia in Rats Tissue Eng Part A 2011.
Smith LE. Bone marrow-derived stem cells preserve cone vision in retinitis pigmentosa J Clin Invest 2004; 114: 755-757.
Suarez-Monteagudo C, Hernandez-Ramirez P, Alvarez-Gonzalez L, Garcia-Maeso I, Cuetara-Bernal K, Castillo-Diaz L, Bringas-Vega ML, Martinez-Aching G, Morales-Chacon LM, Baez-Martin MM, Sanchez-Catasus C, Carballo-Barreda M, Rodriguez-Rojas R, Gomez-Fernandez L, Alberti-Amador E, Macias-Abraham C, Balea ED, Rosales LC, Del Valle PL, Ferrer BB, Gonzalez RM, Bergado JA. Autologous bone marrow stem cell neurotransplantation in stroke patients. An open study Restor Neurol Neurosci 2009; 27: 151-161.
Joe AW, Gregory-Evans K. Mesenchymal stem cells and potential applications in treating ocular disease Curr Eye Res 2010; 35: 941-952.
Joyce N, Annett G, Wirthlin L, Olson S, Bauer G, Nolta JA. Mesenchymal stem cells for the treatment of neurodegenerative disease Regen Med 2010; 5: 933-946.
Ali H, Bahbahani H. Umbilical cord blood stem cells - potential therapeutic tool for neural injuries and disorders Acta Neurobiol Exp (Wars ) 2010; 70: 316-324.
Domanska-Janik K, Habich A, Sarnowska A, Janowski M. Neural commitment of cord blood stem cells (HUCB-NSC/NP): therapeutic perspectives Acta Neurobiol Exp (Wars ) 2006; 66: 279-291.
El-Badri NS. Cord blood stem cells: a fountain of youth for the brain Stem Cells Dev 2006; 15: 293-294.
Erba P, Mantovani C, Kalbermatten DF, Pierer G, Terenghi G, Kingham PJ. Regeneration potential and survival of transplanted undifferentiated adipose tissue-derived stem cells in peripheral nerve conduits J Plast Reconstr Aesthet Surg 2010; 63: e811-e817.
Erba P, Terenghi G, Kingham PJ. Neural differentiation and therapeutic potential of adipose tissue derived stem cells Curr Stem Cell Res Ther 2010; 5: 153-160.
Krabbe C, Zimmer J, Meyer M. Neural transdifferentiation of mesenchymal stem cells--a critical review APMIS 2005; 113: 831-844.
Liu Q, Guan L, Huang B, Li WH, Su Q, Yu M, Xu XP, Luo T, Lin SC, Sun X, Chen M, Chen XG. Adult peripheral blood mononuclear cells transdifferentiate in vitro and integrate into the retina in vivo Cell Biol Int 2011.
Mohammad-Gharibani P, Tiraihi T, Arabkheradmand J. In vitro transdifferentiation of bone marrow stromal cells into GABAergic-like neurons Iran Biomed J 2009; 13: 137-143.
Naghdi M, Tiraihi T, Namin SA, Arabkheradmand J. Transdifferentiation of bone marrow stromal cells into cholinergic neuronal phenotype: a potential source for cell therapy in spinal cord injury Cytotherapy 2009; 11: 137-152.
Roybon L, Ma Z, Asztely F, Fosum A, Jacobsen SE, Brundin P, Li JY. Failure of transdifferentiation of adult hematopoietic stem cells into neurons Stem Cells 2006; 24: 1594-1604.
Zurita M, Bonilla C, Otero L, Aguayo C, Vaquero J. Neural transdifferentiation of bone marrow stromal cells obtained by chemical agents is a short-time reversible phenomenon Neurosci Res 2008; 60: 275-280.
Amariglio N, Hirshberg A, Scheithauer BW, Cohen Y, Loewenthal R, Trakhtenbrot L, Paz N, Koren-Michowitz M, Waldman D, Leider-Trejo L, Toren A, Constantini S, Rechavi G. Donor-derived brain tumor following neural stem cell transplantation in an ataxia telangiectasia patient PLoS Med 2009; 6: e1000029.
Amariglio N, Rechavi G. On the origin of glioneural neoplasms after neural cell transplantation Nat Med 2010; 16: 157-158.
Ben-David U, Benvenisty N. The tumorigenicity of human embryonic and induced pluripotent stem cells Nat Rev Cancer 2011; 11: 268-277.
Saiz A, Graus F. Neurologic complications of hematopoietic cell transplantation Semin Neurol 2010; 30: 287-295.
Capetian P, Dobrossy M, Winkler C, Prinz M, Nikkhah G. To be or not to be accepted: the role of immunogenicity of neural stem cells following transplantation into the brain in animal and human studies Semin Immunopathol 2011.
Ubiali F, Nava S, Nessi V, Frigerio S, Parati E, Bernasconi P, Mantegazza R, Baggi F. Allorecognition of human neural stem cells by peripheral blood lymphocytes despite low expression of MHC molecules: role of TGF-beta in modulating proliferation Int Immunol 2007; 19: 1063-1074.
Zheng XS, Yang XF, Liu WG, Pan DS, Hu WW, Li G. Transplantation of neural stem cells into the traumatized brain induces lymphocyte infiltration Brain Inj 2007; 21: 275-278.
Al NF, Wennersten A, Holmin S, Meijer X, Wahlberg L, Mathiesen T. MHC expression after human neural stem cell transplantation to brain contused rats Neuroreport 2004; 15: 1871-1875.
Barzilay R, Kan I, Ben-Zur T, Bulvik S, Melamed E, Offen D. Induction of human mesenchymal stem cells into dopamine-producing cells with different differentiation protocols Stem Cells Dev 2008; 17: 547-554.
Fricker-Gates RA, Gates MA. Stem cell-derived dopamine neurons for brain repair in Parkinson's disease Regen Med 2010; 5: 267-278.
Shim JW, Park CH, Bae YC, Bae JY, Chung S, Chang MY, Koh HC, Lee HS, Hwang SJ, Lee KH, Lee YS, Choi CY, Lee SH. Generation of functional dopamine neurons from neural precursor cells isolated from the subventricular zone and white matter of the adult rat brain using Nurr1 overexpression Stem Cells 2007; 25: 1252-1262.
Iacovitti L, Donaldson AE, Marshall CE, Suon S, Yang M. A protocol for the differentiation of human embryonic stem cells into dopaminergic neurons using only chemically defined human additives: Studies in vitro and in vivo Brain Res 2007; 1127: 19-25.
Liste I, Garcia-Garcia E, Martinez-Serrano A. The generation of dopaminergic neurons by human neural stem cells is enhanced by Bcl-XL, both in vitro and in vivo J Neurosci 2004; 24: 10786-10795.
Bosch M, Pineda JR, Sunol C, Petriz J, Cattaneo E, Alberch J, Canals JM. Induction of GABAergic phenotype in a neural stem cell line for transplantation in an excitotoxic model of Huntington's disease Exp Neurol 2004; 190: 42-58.
Givogri MI, Bottai D, Zhu HL, Fasano S, Lamorte G, Brambilla R, Vescovi A, Wrabetz L, Bongarzone E. Multipotential neural precursors transplanted into the metachromatic leukodystrophy brain fail to generate oligodendrocytes but contribute to limit brain dysfunction Dev Neurosci 2008; 30: 340-357.
Thomas MG, Stone L, Evill L, Ong S, Ziman M, Hool L. Bone marrow stromal cells as replacement cells for Parkinson's disease: generation of an anatomical but not functional neuronal phenotype Transl Res 2011; 157: 56-63.
Brundin P, Barker RA, Parmar M. Neural grafting in Parkinson's disease Problems and possibilities Prog Brain Res 2010; 184: 265-294.
Lecanu L. Sex, the underestimated potential determining factor in brain tissue repair strategy Stem Cells Dev 2011.
Meyer AK, Maisel M, Hermann A, Stirl K, Storch A. Restorative approaches in Parkinson's Disease: which cell type wins the race? J Neurol Sci 2010; 289: 93-103.
Waldron J, Lecanu L. Age and sex-difference in neural stem cells transplantation outcome: a descriptive study in rats. Stem Cells Cloning Adv Appl 2011; 4: 25-37.
Arias-Carrion O, Hernandez-Lopez S, Ibanez-Sandoval O, Bargas J, Hernandez-Cruz A, Drucker-Colin R. Neuronal precursors within the adult rat subventricular zone differentiate into dopaminergic neurons after substantia nigra lesion and chromaffin cell transplant J Neurosci Res 2006; 84: 1425-1437.
Tonellato PJ, Crawford JM, Boguski MS, Saffitz JE. A national agenda for the future of pathology in personalized medicine: report of the proceedings of a meeting at the Banbury Conference Center on genome-era pathology, precision diagnostics, and preemptive care: a stakeholder summit Am J Clin Pathol 2011; 135: 668-672.
Callaway E. Stem-cell progress Nature 2010; 468: 746.
Helmy KY, Patel SA, Silverio K, Pliner L, Rameshwar P. Stem cells and regenerative medicine: accomplishments to date and future promise Ther Deliv 2010; 1: 693-705.
Patel SA, King CC, Lim PK, Habiba U, Dave M, Porecha R, Rameshwar P. Personalizing Stem Cell Research and Therapy: The Arduous Road Ahead or Missed Opportunity? Curr Pharmacogenomics Person Med 2010; 8: 25-36.
Lane EL, Bjorklund A, Dunnett SB, Winkler C. Neural grafting in Parkinson's disease unraveling the mechanisms underlying graft-induced dyskinesia Prog Brain Res 2010; 184: 295-309.
Deda H, Inci MC, Kurekci AE, Sav A, Kayihan K, Ozgun E, Ustunsoy GE, Kocabay S. Treatment of amyotrophic lateral sclerosis patients by autologous bone marrow-derived hematopoietic stem cell transplantation: a 1-year follow-up Cytotherapy 2009; 11: 18-25.
Fornai F, Meininger V, Silani V. Future therapeutical strategies dictated by pre-clinical evidence in ALS Arch Ital Biol 2011; 149: 169-174.
Martinez HR, Gonzalez-Garza MT, Moreno-Cuevas JE, Caro E, Gutierrez-Jimenez E, Segura JJ. Stem-cell transplantation into the frontal motor cortex in amyotrophic lateral sclerosis patients Cytotherapy 2009; 11: 26-34.
Mazzini L, Ferrero I, Luparello V, Rustichelli D, Gunetti M, Mareschi K, Testa L, Stecco A, Tarletti R, Miglioretti M, Fava E, Nasuelli N, Cisari C, Massara M, Vercelli R, Oggioni GD, Carriero A, Cantello R, Monaco F, Fagioli F. Mesenchymal stem cell transplantation in amyotrophic lateral sclerosis: A Phase I clinical trial Exp Neurol 2010; 223: 229-237.
Silani V, Calzarossa C, Cova L, Ticozzi N. Stem cells in amyotrophic lateral sclerosis: motor neuron protection or replacement? CNS Neurol Disord Drug Targets 2010; 9: 314-324.
Gamez J, Carmona F, Raguer N, Ferrer-Sancho J, Martin-Henao GA, Marti-Beltran S, Badia M, Gratacos M, Rodriguez-Gonzalez E, Seoane JL, Pallero-Castillo M, Burgos R, Puiggros C, Pasarin A, Bori-Fortuny I. Cellular transplants in amyotrophic lateral sclerosis patients: an observational study Cytotherapy 2010; 12: 669-677.
Bachoud-Levi AC, Remy P, Nguyen JP, Brugieres P, Lefaucheur JP, Bourdet C, Baudic S, Gaura V, Maison P, Haddad B, Boisse MF, Grandmougin T, Jeny R, Bartolomeo P, Dalla BG, Degos JD, Lisovoski F, Ergis AM, Pailhous E, Cesaro P, Hantraye P, Peschanski M. Motor and cognitive improvements in patients with Huntington's disease after neural transplantation Lancet 2000; 356: 1975-1979.
Cicchetti F, Soulet D, Freeman TB. Neuronal degeneration in striatal transplants and Huntington's disease: potential mechanisms and clinical implications Brain 2011; 134: 641-652.
Keene CD, Sonnen JA, Swanson PD, Kopyov O, Leverenz JB, Bird TD, Montine TJ. Neural transplantation in Huntington disease: long-term grafts in two patients Neurology 2007; 68: 2093-2098.
Lee HJ, Lee JK, Lee H, Shin JW, Carter JE, Sakamoto T, Jin HK, Bae JS. The therapeutic potential of human umbilical cord blood-derived mesenchymal stem cells in Alzheimer's disease Neurosci Lett 2010; 481: 30-35.
Taupin P. Neurogenesis, NSCs, pathogenesis and therapies for Alzheimer's disease Front Biosci (Schol Ed) 2011; 3: 178-190.
Zhongling F, Gang Z, Lei Y. Neural stem cells and Alzheimer's disease: challenges and hope Am J Alzheimers Dis Other Demen 2009; 24: 52-57.
Scolding N. Adult stem cells and multiple sclerosis Cell Prolif 2011; 44 Suppl 1: 35-38.
Uccelli A, Laroni A, Freedman MS. Mesenchymal stem cells for the treatment of multiple sclerosis and other neurological diseases Lancet Neurol 2011; 10: 649-656.
Zeher M, Papp G, Szodoray P. Autologous haemopoietic stem cell transplantation for autoimmune diseases Expert Opin Biol Ther 2011.
Bretzner F, Gilbert F, Baylis F, Brownstone RM. Target populations for first-in-human embryonic stem cell research in spinal cord injury Cell Stem Cell 2011; 8: 468-475.
Dasari VR, Spomar DG, Gondi CS, Sloffer CA, Saving KL, Gujrati M, Rao JS, Dinh DH. Axonal remyelination by cord blood stem cells after spinal cord injury J Neurotrauma 2007; 24: 391-410.
Adler R. Curing blindness with stem cells: hope, reality, and challenges Adv Exp Med Biol 2008; 613: 3-20.
Freed CR, Greene PE, Breeze RE, Tsai WY, DuMouchel W, Kao R, Dillon S, Winfield H, Culver S, Trojanowski JQ, Eidelberg D, Fahn S. Transplantation of embryonic dopamine neurons for severe Parkinson's disease N Engl J Med 2001; 344: 710-719.
Hauser RA, Freeman TB, Snow BJ, Nauert M, Gauger L, Kordower JH, Olanow CW. Long-term evaluation of bilateral fetal nigral transplantation in Parkinson disease Arch Neurol 1999; 56: 179-187.
Ma Y, Tang C, Chaly T, Greene P, Breeze R, Fahn S, Freed C, Dhawan V, Eidelberg D. Dopamine cell implantation in Parkinson's disease: long-term clinical and (18)F-FDOPA PET outcomes J Nucl Med 2010; 51: 7-15.
Olanow CW, Goetz CG, Kordower JH, Stoessl AJ, Sossi V, Brin MF, Shannon KM, Nauert GM, Perl DP, Godbold J, Freeman TB. A double-blind controlled trial of bilateral fetal nigral transplantation in Parkinson's disease Ann Neurol 2003; 54: 403-414.
Lindvall O, Rehncrona S, Brundin P, Gustavii B, Astedt B, Widner H, Lindholm T, Bjorklund A, Leenders KL, Rothwell JC, Frackowiak R, Marsden D, Johnels B, Steg G, Freedman R, Hoffer BJ, Seiger A, Bygdeman M, Stromberg I, Olson L. Human fetal dopamine neurons grafted into the striatum in two patients with severe Parkinson's disease. A detailed account of methodology and a 6-month follow-up Arch Neurol 1989; 46: 615-631.
Lindvall O, Brundin P, Widner H, Rehncrona S, Gustavii B, Frackowiak R, Leenders KL, Sawle G, Rothwell JC, Marsden CD, . Grafts of fetal dopamine neurons survive and improve motor function in Parkinson's disease Science 1990; 247: 574-577.
Dobrossy M, Busse M, Piroth T, Rosser A, Dunnett S, Nikkhah G. Neurorehabilitation with neural transplantation Neurorehabil Neural Repair 2010; 24: 692-701.
Mills KR. The natural history of central motor abnormalities in amyotrophic lateral sclerosis Brain 2003; 126: 2558-2566.
Gaura V, Bachoud-Levi AC, Ribeiro MJ, Nguyen JP, Frouin V, Baudic S, Brugieres P, Mangin JF, Boisse MF, Palfi S, Cesaro P, Samson Y, Hantraye P, Peschanski M, Remy P. Striatal neural grafting improves cortical metabolism in Huntington's disease patients Brain 2004; 127: 65-72.
Grinnemo KH, Sylven C, Hovatta O, Dellgren G, Corbascio M. Immunogenicity of human embryonic stem cells Cell Tissue Res 2008; 331: 67-78.
Sobani ZA, Quadri SA, Enam SA. Stem cells for spinal cord regeneration: Current status Surg Neurol Int 2010; 1: 93.
Zurita M, Otero L, Aguayo C, Bonilla C, Ferreira E, Parajon A, Vaquero J. Cell therapy for spinal cord repair: optimization of biologic scaffolds for survival and neural differentiation of human bone marrow stromal cells Cytotherapy 2010; 12: 522-537.
Shen CC, Lin CH, Yang YC, Chiao MT, Cheng WY, Ko JL. Intravenous implanted neural stem cells migrate to injury site, reduce infarct volume, and improve behavior after cerebral ischemia Curr Neurovasc Res 2010; 7: 167-179.
Aoki H, Hara A, Niwa M, Yamada Y, Kunisada T. In vitro and in vivo differentiation of human embryonic stem cells into retina-like organs and comparison with that from mouse pluripotent epiblast stem cells Dev Dyn 2009; 238: 2266-2279.
Arnhold S, Klein H, Semkova I, Addicks K, Schraermeyer U. Neurally selected embryonic stem cells induce tumor formation after long-term survival following engraftment into the subretinal space Invest Ophthalmol Vis Sci 2004; 45: 4251-4255.
Chen M, Chen Q, Sun X, Shen W, Liu B, Zhong X, Leng Y, Li C, Zhang W, Chai F, Huang B, Gao Q, Xiang AP, Zhuo Y, Ge J. Generation of retinal ganglion-like cells from reprogrammed mouse fibroblasts Invest Ophthalmol Vis Sci 2010; 51: 5970-5978.
Francis PJ, Wang S, Zhang Y, Brown A, Hwang T, McFarland TJ, Jeffrey BG, Lu B, Wright L, Appukuttan B, Wilson DJ, Stout JT, Neuringer M, Gamm DM, Lund RD. Subretinal transplantation of forebrain progenitor cells in nonhuman primates: survival and intact retinal function Invest Ophthalmol Vis Sci 2009; 50: 3425-3431.
Klassen H, Schwartz PH, Ziaeian B, Nethercott H, Young MJ, Bragadottir R, Tullis GE, Warfvinge K, Narfstrom K. Neural precursors isolated from the developing cat brain show retinal integration following transplantation to the retina of the dystrophic cat Vet Ophthalmol 2007; 10: 245-253.
Levkovitch-Verbin H, Sadan O, Vander S, Rosner M, Barhum Y, Melamed E, Offen D, Melamed S. Intravitreal injections of neurotrophic factors secreting mesenchymal stem cells are neuroprotective in rat eyes following optic nerve transection Invest Ophthalmol Vis Sci 2010; 51: 6394-6400.
Lund RD, Ono SJ, Keegan DJ, Lawrence JM. Retinal transplantation: progress and problems in clinical application J Leukoc Biol 2003; 74: 151-160.
Seiler MJ, Aramant RB, Thomas BB, Peng Q, Sadda SR, Keirstead HS. Visual restoration and transplant connectivity in degenerate rats implanted with retinal progenitor sheets Eur J Neurosci 2010; 31: 508-520.
Wang DY, Wu SC, Lin SP, Hsiao SH, Chung TW, Huang YY. Evaluation of transdifferentiation from mesenchymal stem cells to neuron-like cells using microfluidic patterned co-culture system Biomed Microdevices 2011; 13: 517-526.
Wang S, Girman S, Lu B, Bischoff N, Holmes T, Shearer R, Wright LS, Svendsen CN, Gamm DM, Lund RD. Long-term vision rescue by human neural progenitors in a rat model of photoreceptor degeneration Invest Ophthalmol Vis Sci 2008; 49: 3201-3206.
Yang Z, Li K, Yan X, Dong F, Zhao C. Amelioration of diabetic retinopathy by engrafted human adipose-derived mesenchymal stem cells in streptozotocin diabetic rats Graefes Arch Clin Exp Ophthalmol 2010; 248: 1415-1422.
Maruska KP, Fernald RD. Steroid receptor expression in the fish inner ear varies with sex, social status, and reproductive state BMC Neurosci 2010; 11: 58.
Yamada S, Noguchi D, Ito H, Yamanouchi K. Sex and regional differences in decrease of estrogen receptor alpha-immunoreactive cells by estrogen in rat hypothalamus and midbrain Neurosci Lett 2009; 463: 135-139.
Zhang JQ, Cai WQ, Zhou DS, Su BY. Distribution and differences of estrogen receptor beta immunoreactivity in the brain of adult male and female rats Brain Res 2002; 935: 73-80.
Hisasue S, Seney ML, Immerman E, Forger NG. Control of cell number in the bed nucleus of the stria terminalis of mice: role of testosterone metabolites and estrogen receptor subtypes J Sex Med 2010; 7: 1401-1409.
Kudwa AE, Bodo C, Gustafsson JA, Rissman EF. A previously uncharacterized role for estrogen receptor beta: defeminization of male brain and behavior Proc Natl Acad Sci U S A 2005; 102: 4608-4612.
Kudwa AE, Michopoulos V, Gatewood JD, Rissman EF. Roles of estrogen receptors alpha and beta in differentiation of mouse sexual behavior Neuroscience 2006; 138: 921-928.
Brannvall K, Korhonen L, Lindholm D. Estrogen-receptor-dependent regulation of neural stem cell proliferation and differentiation Mol Cell Neurosci 2002; 21: 512-520.
Fowler CD, Johnson F, Wang Z. Estrogen regulation of cell proliferation and distribution of estrogen receptor-alpha in the brains of adult female prairie and meadow voles J Comp Neurol 2005; 489: 166-179.
Kishi Y, Takahashi J, Koyanagi M, Morizane A, Okamoto Y, Horiguchi S, Tashiro K, Honjo T, Fujii S, Hashimoto N. Estrogen promotes differentiation and survival of dopaminergic neurons derived from human neural stem cells J Neurosci Res 2005; 79: 279-286.
Martinez-Cerdeno V, Noctor SC, Kriegstein AR. Estradiol stimulates progenitor cell division in the ventricular and subventricular zones of the embryonic neocortex Eur J Neurosci 2006; 24: 3475-3488.
Suzuki S, Gerhold LM, Bottner M, Rau SW, Dela CC, Yang E, Zhu H, Yu J, Cashion AB, Kindy MS, Merchenthaler I, Gage FH, Wise PM. Estradiol enhances neurogenesis following ischemic stroke through estrogen receptors alpha and beta J Comp Neurol 2007; 500: 1064-1075.
Wang JM, Liu L, Brinton RD. Estradiol-17beta-induced human neural progenitor cell proliferation is mediated by an estrogen receptor beta-phosphorylated extracellularly regulated kinase pathway Endocrinology 2008; 149: 208-218.
Okada M, Murase K, Makino A, Nakajima M, Kaku T, Furukawa S, Furukawa Y. Effects of estrogens on proliferation and differentiation of neural stem/progenitor cells Biomed Res 2008; 29: 163-170.
Okada M, Makino A, Nakajima M, Okuyama S, Furukawa S, Furukawa Y. Estrogen Stimulates Proliferation and Differentiation of Neural Stem/Progenitor Cells through Different Signal Transduction Pathways Int J Mol Sci 2010; 11: 4114-4123.
Sun H, Wang H, Hu S. Effects of estrogen on diverse stem cells and relevant intracellular mechanisms Sci China Life Sci 2010; 53: 542-547.
Leskela HV, Olkku A, Lehtonen S, Mahonen A, Koivunen J, Turpeinen M, Uusitalo J, Pelkonen O, Kangas L, Selander K, Lehenkari P. Estrogen receptor alpha genotype confers interindividual variability of response to estrogen and testosterone in mesenchymal-stem-cell-derived osteoblasts Bone 2006; 39: 1026-1034.
Barker JM, Galea LA. Repeated estradiol administration alters different aspects of neurogenesis and cell death in the hippocampus of female, but not male, rats Neuroscience 2008; 152: 888-902.
Waldron J, McCourty AM, Lecanu L. Neural stem cell sex dimorphism in aromatase (CYP19) expression: a basis for differential neural fate. Stem Cells Cloning Adv Appl 2010; 3: 175-182.
Martins AH, Alves JM, Trujillo CA, Schwindt TT, Barnabe GF, Motta FL, Guimaraes AO, Casarini DE, Mello LE, Pesquero JB, Ulrich H. Kinin-B2 receptor expression and activity during differentiation of embryonic rat neurospheres Cytometry A 2008; 73: 361-368.
Sillat T, Pollanen R, Lopes JR, Porola P, Ma G, Korhonen M, Konttinen YT. Intracrine androgenic apparatus in human bone marrow stromal cells J Cell Mol Med 2009; 13: 3296-3302.
Morgan DE, Crittenden SL, Kimble J. The C. elegans adult male germline: stem cells and sexual dimorphism Dev Biol 2010; 346: 204-214.
Limke TL, Rao MS. Neural stem cells in aging and disease J Cell Mol Med 2002; 6: 475-496.
Limke TL, Rao MS. Neural stem cell therapy in the aging brain: pitfalls and possibilities J Hematother Stem Cell Res 2003; 12: 615-623.
Limke TL, Cai J, Miura T, Rao MS, Mattson MP. Distinguishing features of progenitor cells in the late embryonic and adult hippocampus Dev Neurosci 2003; 25: 257-272.
Maslov AY, Barone TA, Plunkett RJ, Pruitt SC. Neural stem cell detection, characterization, and age-related changes in the subventricular zone of mice J Neurosci 2004; 24: 1726-1733.
Kuhn HG, Dickinson-Anson H, Gage FH. Neurogenesis in the dentate gyrus of the adult rat: age-related decrease of neuronal progenitor proliferation J Neurosci 1996; 16: 2027-2033.
Sato K, Hayashi T, Sasaki C, Iwai M, Li F, Manabe Y, Seki T, Abe K. Temporal and spatial differences of PSA-NCAM expression between young-adult and aged rats in normal and ischemic brains Brain Res 2001; 922: 135-139.
Kudwa AE, Gustafsson JA, Rissman EF. Estrogen receptor beta modulates estradiol induction of progestin receptor immunoreactivity in male, but not in female, mouse medial preoptic area Endocrinology 2004; 145: 4500-4506.
Kudwa AE, Harada N, Honda SI, Rissman EF. Regulation of progestin receptors in medial amygdala: estradiol, phytoestrogens and sex Physiol Behav 2009; 97: 146-150.
Mayack SR, Shadrach JL, Kim FS, Wagers AJ. Systemic signals regulate ageing and rejuvenation of blood stem cell niches Nature 2010; 463: 495-500.
Niikura Y, Niikura T, Wang N, Satirapod C, Tilly JL. Systemic signals in aged males exert potent rejuvenating effects on the ovarian follicle reserve in mammalian females Aging (Albany NY) 2010; 2: 999-1003.