Cell adhesion to the extracellular matrix (ECM) is primarily mediated through integrin receptors and contributes to numerous physiological and pathological processes. It would be most attractive for biomedical implants to interact with the surrounding host tissue in a manner which promotes the healing process, beginning with cell adhesion and growth. This calls for a good understanding of the mechanisms by which the ECM is involved in the control and organization of cellular processes for wound healing and tissue regeneration. Alongside the critically important fields of cell signalling, circulating hormones, cytokines and extracellular proteases, the role of the structure, organization and stiffness of the ECM can be overlooked. It is the intention of this review to discuss the various approaches that have been used to mimic the structural and dynamic aspects of native ECM proteins, and how these may modulate cell behaviour. It is clear that molecular biology has much to contribute, since protein constructs are now routinely expressed, circumventing the need to purify protein molecules (e.g. collagen, laminin, vitronectin and fibronectin) from plasma or tissue. Thus, protein engineering has become an essential tool for development of multi-functional mimics of the ECM. Since integrins mediate the signalling pathways involved in cell-ECM attachment, and subsequent self-renewal/differentiation in the case of embryonic stem cells, these cell surface receptors will be briefly introduced. The review will then move onto the key protein components of the ECM and contemporary studies which have utilised this knowledge to generate novel biomaterials able to control cell behaviour.
2. Integrin receptors
Integrin receptors are recognized as one of the most important cell surface adhesion and signalling receptors, and are widely expressed in many cell types such as smooth muscle, endothelium, platelets, and osteoclasts. Integrins are a family of heterodimers consisting of two transmembrane subunit proteins (α and β) that are non-covalently bound but inter-dependent for correct ligand binding. Eighteen α and eight β subunits have been listed in humans to date with 24 dimeric combinations identified, each having distinct binding profiles to the various extracellular ligands. For instance, osteoclasts bind collagen via α1β1 and α2β1 integrins whereas fibroblasts bind fibronectin (FN) and vitronectin via α5β1 and αvβ3 integrins, respectively. Several integrins can recognize the same ligands with varying affinity. Both α and β subunits have large extracellular domains composed of a membrane distal, globular head (~ 700-1100 residues). The crystal structures of the extracellular segment of αvβ3 in ligand-occupied and non-occupied states have been exceptionally important in understanding the ligand/receptor recognition process at the atomic level.
Electron micrographs of the complete ectodomain, which includes the headpiece with the ‘lower leg’ calf and epidermal growth factor (EGF)-like domains of the α and β subunits, respectively, have been acquired for integrin αIIbβ3 in its rested and activated state. It appears that the integrin receptors are in a compact ‘bent’ form when inactive, which results in the head domains (the β-propeller and the β-I domain of the α and β subunits, respectively) lying close to the cell membrane, and an extended ‘standing’ conformation when activated. A low resolution electron micrograph structure of a recombinant fibronectin fragment bound to the ‘headpiece’ (the head domains with the thigh and hybrid/plexin-semaphorin-integrin (PSI) domains of the α and β subunits, respectively) of integrin α5β1 has also been published. The dimensions of the integrin ectodomain in the crystal structure are approximately 80 × 90 × 110 Å and a similar estimation can be inferred from the accompanying low resolution electron microscopy (EM) structures. Superposing the crystal structure onto the electron micrographs has also been informative to understanding the large conformational changes associated with the α/β subunits upon ligand binding and activation. Both the α and β subunits span the cell membrane and interact with the actin cytoskeleton via vinculin or talin during cell signalling.
The binding of a ligand to an integrin receptor causes tyrosine phosphorylation of the β subunit cytosolic domain by v-src. This in turn facilitates the binding of cell actin filaments and intermediary proteins (vinculin and talin) which form complexes associated with the focal adhesion structures. Thus, integrins are thought to exist on the cell surface in an inactive form and can be activated either by binding ECM (outside-in signalling), but also by intracellular signalling (inside-out signalling). Outside-in signalling involves cell adhesion, proliferation, migration, differentiation and apoptosis. Inside-out signalling involves, for example, platelet aggregate via αIIbβ3 activation leading to haemostasis. Integrin receptors may alternate between active and inactive states by conformational changes of the ligand binding sites from a high affinity state (active) to a low affinity state (inactive).
Integrin receptors are usually present at 10-100 fold higher concentrations on the cell surface than other non adhesive receptors. Moreover, it has been noted that integrins cluster when binding to their ligands, which can be observed at focal adhesions by immuno-microscopy. It is likely that the ECM binds a large number of integrins in a polyvalent manner, increasing binding affinity. However, tight regulation over integrin recruitment activation state and binding affinity must be maintained in order to facilitate transitional cell detachment during cell migration. In association with the formation of focal adhesions is a force dependent “adhesion strengthening” process. This adhesion reinforcement can be induced through the use of synthetic ligand matrices as discussed further below.
3. Key protein components of the ECM
Vitronectin is a small multifunctional adhesive glycoprotein which is mostly present in the blood as a monomer, but can also be found as a multimer (up to 16-mer) in the ECM of various tissues. The polypeptide chains often can be in the form of two molecular species of around 60 and 75 kDa, of which up to 30% is a result of glycosylation. The recognized cell binding domain sequence ‘arginine-glycine-aspartic acid’ (‘RGD’) is present, facilitating binding to the integrin subtypes αvβ3 and αvβ5 and through this, cell adhesion is initiated. The formation of multimeric vitronectin clusters has been shown to increase heparin binding when compared to the monomeric form. These multimers can also form following binding of the molecule to plasminogen activity inhibitor PAI-1. More recently, it has been shown that to achieve enhancement of cell adhesion and spreading, oligomerisation must be initiated and that this process requires the heparin binding domain. A newly engineered construct called sVnHBD represents the minimal vitronectin domain requirement for integrin dependent cell adhesion and spreading function of vitronectin (Fig. 1). Senile plaques in the Alzheimer-diseased brain have been shown to have vitronectin immunoreactivity. Further study suggested that vitronectin aggregation mirrors that of amyloid protein, the misfolded products of which may therefore contribute to age-related amyloid disease.
Collagen is a multichain glycoprotein constructed from three polypeptide units forming a unique triple-helix conformation. It is a major structural component if the ECM and the most abundant of the structural proteins. There are at least 20 different kinds of genetically distinct molecules which based on structural features can be categorized as fibril forming (types I, II, III, V and XI) and network-forming (types IV, VIII and X), with type I being the most common in the ECM. This key component of the ECM is a versatile substrate for supporting cell proliferation and differentiation. Collagen in itself represents a very large, active field of research, the scope of which cannot be given justice in this review; the reader is therefore directed to previous, excellent reviews such as that by. Structural and functional collagen mimetic peptides (CMPs) harboring integrin binding motifs (GFOGER) to achieve ‘bioadhesiveness’ have proven useful in the synthesis of biologically relevant matrices when used in combination with polymeric scaffolds, for the culture of hepatic cells towards liver tissue engineering. A recent innovation has been to embed collagen microfibres with defined orientations and densities in engineered elastin-like matrices, yielding thin lamellae with a specified stiffness, which have been tested
Interactions via the basement membrane are mediated by the engagement of laminin with several integrins including α3β1 α6β1 α7β1 α6β4. The structural conformation of laminin involves three non-identical polypeptide chains: α, β and γ, which form cross shaped molecules in mammals. There are five α, three β and three γ subunits identified which can combine to produce 15 isoforms. The function of laminin is determined by the subunit combination which can be selective for multiple cell adhesive regions including the RGD motif, which is located on the amino-terminal half of the α chain. It has been determined that integrin binding is specifically governed by the α chains. The mouse laminin α1 chain 2719-2730 (RKRLQVQLSIRT, termed AG73) is a syndecan-binding peptide which promotes cell adhesion, migration and invasion. In an elegant study demonstrating the importance of using a composite approach to mimicry of the ECM, AG73 was combined with collagen as a cell substrate for cell culture. Human dermal fibroblasts (HDFs) developed strong actin filaments when grown on AG73/collagen substrates but not on AG73 alone or substrates with low collagen concentrations (Fig. 2). The full importance of laminin is still emerging; for example, direct interaction between laminin and retinal ganglion cells is required for full axon emergence and orientation
In humans, the FN gene is comprised of 46 exons within an 82 kb gene and is located on chromosome 2 (2q34). Due to extensive alternative splicing of FN pre-mRNA, there are 20 potential isoforms of FN leading to variants with different functions. The occurrence of splicing gives rise to insoluble cell associated FN (cFN) and soluble plasma FN (pFN). FN usually exists as a dimer of about 500 kDa composed of two subunits linked by a disulphide bond near their C-terminus. Isopeptide bonds form between FN dimers in the N-terminal domain to form insoluble (cellular) cFN. The association of FN with cell surface integrins is the main motivator behind this process.
The FN monomers consist of three types of repeating unit, termed type I, type II and type III. Each repeating unit has a different number of amino acid residues with type I usually consisting of about 40, type II comprising of approximately 60 and type III having around 90 amino acids. Furthermore, type I and II each have two intrachain disulphide bonds while type III domains do not contain any disulphides. Typically, FN contains 12 type I repeats, each with stacked β-sheets enclosing a hydrophobic core. There are two type II repeats comprising disulphide linked perpendicular anti-parallel β-sheets. Type III repeats make up approx. 90 % of the FN sequence, with 15 to 17 repeats.
There are at least 11 heterodimeric integrins which FN can bind to in a cell and tissue specific manner, the best characterised of these are integrins α5β1 and αvβ3. FN also contains multiple binding sites for other ECM compounds including heparin and collagen. The short polypeptide sequence, RGD, located on the peptide loop in the 10th FN type III domain (FIII10) is the key attachment site for integrins. In addition to this sequence, a “synergy site” (PHSRN) has been located to the 9th FN type III domain (FIII9), which is required for
maximum binding to integrin α5β1. Conformational stabilisation of FIII9 occurs through interaction with its neighbouring domains, particularly the 8th type III FN domain (FIII8). The domain-domain mobility between FIII9 and FIII10 is unusually high; constricting this mobility by introducing an interdomain disulphide bridge brings about a change in the relative orientation between the RGD- and PHSRN-bearing loops and a decrease in α5β1 binding avidity (Fig. 3). Thus, while cell adhesion and spreading can be controlled through site-directed mutation of key residues in binding motifs, an alternative route would be to subtly alter the FIII9/FIII10 scaffold architecture.
4. Temporal changes to the ECM
Interaction of cells with artificial ECM matrices
The concept of temporal regulation of cell adhesion in synthetic scaffolds was also introduced for human mesenchymal stem cell (hMSC) culture. This built on data showing that upregulation the matrix metalloproteinase MMP-13 by hMSCs was coincident with down regulation of FN deposition, as normally required for chondrogenesis. The polyethylene glycol (PEG)-peptide matrices developed were interesting because for the first time, biomaterials with an inherent ability to down regulate cell adhesion were demonstrated. The PEG hydrogels were tethered to peptides harbouring the MMP-13 cleavage site and RGD motif (full sequence, CPENFFGRGDSG), and then utilised to encapsulate hMSCs for culture (Fig. 4). The hMSCs encapsulated in either cleavable or non-cleavable (control) PEG-RGD hydrogels and cultured in chondrogenic media were seen to maintain their viability over 11 days. However, over the following 2 weeks, the hMSCs cultured in cleavable PEG-RGD substrates lost their viability by around 66% because MMP-13 production caused RGD cleavage from the PEG polymeric scaffold.
Photo-activated cleavage is an attractive approach since it is more efficient and controllable than endogenous of exogenous enzyme mediate cleavage. Previously, photo-activated cleavage of RGD from 2-dimensional (2-D) cell substrates has also been achieved but only to switch cell adhesion ‘on’ or ‘off’. The development of selectively adhesive plasticware in which the use of UV light could control the adhesion of cells was achieved by the use of photo-caged RGD based peptide. This has been done in two comparably different manners. Firstly, a carboxylic acid side chain, 3-(4,5-Dimethoxy-2nitrophenyl)-2-butyl ester (DMNPB), was introduced onto the aspartic acid of RGD. The introduction of this may have affected the steric hindrance or conformation of the peptide which reduced binding affinity, shown by reduced fibroblast cell attachment. The irradiation of the plate cleaved the DMNPB, this was demonstrated by increased DMNPB in solution measured by UV absorbance following UV incubation at 364 nm for 2 hours, and increased spreading of fibroblasts plated onto surface. Direct blocking of the RGD motif using a 2-nitrobenzyl group has also been employed by introduction of nitrobenzyl at the amide bond between the Gly and Arg. The placement of the group here essentially switched off the binding capability, which was then restored by UV irradiation; this was demonstrated in an exposure dependant manner. A non-linear relationship between exposure time and cell adhesion was found, suggesting that there may be an upper limit for adhesion. Although not detailed in these studies, there is the potential for cell damage from heat produced by the light source. The use of a small nitrobenzyl group would preferable in a hope that it would not irreversibly alter the binding peptide. The coupling of this with integrin selective binding peptides/proteins would be interesting for further studies to control 2-D and 3-dimentional (3-D) tissue matrices.
5. Generating a polyvalent integrin ligand display
5.1. Recombinant fibronectin ligands and the ‘RGD’ motif
Organization of FN fibrils in the extracellular matrix renders a polyvalent display of ligand to cell surface integrin receptors. Previous work has shown that integrin-driven polymerization of soluble FN is dependent on extension of the FN monomer in order to expose self-associating sites. The resultant fibrils are able to undergo extension/contraction over a four-fold change in length, yielding an elastic matrix. Such dynamic movements within the cell matrix inevitably change both the matrix rigidity and the spatial arrangement of the ligand display ‘seen’ by the cell. Interestingly, fibroblasts have been shown to probe the elasticity of their supporting matrix, responding to greater elasticity with increased motility and protruding lamellipodia but decreased ‘spread’ morphology. A key driver in biomaterials research has been the search for suitable mimics to the dynamic nature of the ECM, with some solutions described above. A vast amount of work has focussed on the RGD motif which is found in multiple ECM proteins and is probably the most recognized peptide sequence associated with cell adhesion. It is therefore a predictable target for simulated cell adhesion to surfaces.
However, there have been recent challenges to the extent to which peptides like RGD can accurately mimic the local cellular environment, despite ingenious engineering approaches. One concern is the ability of peptides to selectively bind the different integrin subtypes, and here protein fragments may prove more useful since they have been shown to distinguish between integrin α5β1 and α5β1 subtypes. Similarly, the affinity of binding to the several integrin receptors which recognize the sequence may be modulated by the conformation of the RDG loop and the surrounding amino acids within the protein. There are two fibronectin fragments which are commonly reported in the literature. The first is a domain pair encompassing the 9th-10th type III FN domains (FIII9-10), wherein a key substitution of proline for leucine-1408 in FIII9 is used to increase the conformational stability of this domain by introducing a Pro-Pro pair (cf. Fig. 3). This mutant, termed FIII9’10, has been used to generate polyvalent ECM mimics and support embryonic stem cells, discussed below. The second fragment is larger and encompasses the 7th-10th type III FN domains (FIII7-10).
5.2. Monomeric versus multimeric ligands
Since FN exists in the ECM as a dimer presenting six cell adhesion domains within a small area, when emulating this polyvalent display it would be prudent to strive for a similar tactic, suggesting that multimeric, clustered ligands would be preferable. Multimeric ligands displaying the RGD motif have been shown to better support cell motility and migration compared to monomeric ligands. Furthermore, higher ligand density and cluster size has been shown to increased the strength of attachment of fibroblast cells. Although simple non-clustered RGD ligands were capable of supporting cell attachment, they were unable to exhibit full spreading of fibroblast cells. An alternative approach to generating a polyvalent RGD display as has been the self-assembly of β-sheet peptides harboring RGD which form regular nanofibre structures. Some related amphiphilic peptide assemblies have involved elaborate work to include both the RGD and PHSRN peptide motifs, generating fibres around 10 nm in diameter and several microns in length. Such self-assembly approaches challenge the need to coat non-functional polymeric 3-D scaffolds with bioadhesive peptides/proteins, but may be limited with regard to scale-up/cost for clinical application.
However, as mentioned above, RGD peptides have certain limitations in their ability to recapitulate key aspects of the ECM, particularly integrin subtype selection. The challenge is to design self-assembling systems for protein fragments, but taking into account their labile nature: that is, one cannot simply expose proteins to synthetic chemistry which involves organic solvents likely to unfold the protein fragment. Ideally, the self assembly of proteins would involve the independent formation of an organized stable structure through non-covalent forces such as hydrogen bonds, ionic bonds and van der Waals interactions. The application of self assembling proteins is diverse and has included the pH induced formation of a self assembled artificial protein hydrogels. Application to biomimetic materials has been explored by compiling helical coiled-coils for di-, tri- and tetra-helical multimers. The stability and order of these coiled coil structures has been encouraging for application towards functional biomaterials.
The construction of a coiled coil system involving FN has been achieved by selective mutation of key amino acids in a heptad repeat of the GCN4 leucine zipper helix to allow for direct self assembly of parallel coiled coils. A spacer based on an IgG hinge was included to prevent steric clashes between bound integrin receptors (i.e. N-FIII9’10-hinge-coiled coil-C). In this case, the mutant fibronectin fragment FIII9’10 was utilized because of its previously reported conformational stability. In this way, the FIII9’10-dimer, -trimer and -tetramer were constructed, and the effect of these multimeric systems on baby hamster kidney cells and primary endometrial stromal cells was analysed. For both fibroblast and stromal cell lines, increased cell attachment and spreading were observed with increasing multimerisation of FIII9’10. The morphology of the spread stromal cells on the FIII9’10-tetramer recapitulated their spread morphology on FN (Fig. 5), and suggests that multimeric constructs will have a role to play in endometrial tissue engineering. Translation of these cell data from 2-D ligand displays to 3-D scaffolds under perfusion culture is currently underway.
6. Non specific versus directed protein adsorption
Non-specific adsorption of a protein to a surface usually involves the incubation of the desired surface in a protein solution. The protein adsorbs to the surface through non specific interactions such as hydrophobic and electrostatic forces. Directed protein adsorption through covalent surface modification involves the attachment of mechanisms to the ligand display. These can be in the form of, polymer side chains, self assembling monolayers or components of a lipid bilayer. The generation of model substrates which present defined binding motifs, such as RGD, from the ECM are subjected to many issues. The importance of ligand conformation may be compromised by the immobilized proteins undergoing denaturation or adsorption in the ‘incorrect’ orientation (i.e. resulting in the ligand not being available for receptor binding). In order to have well defined substrates with reproducible results these changes during adsorption should be characterized and/or controlled.
The non-specific adsorption of a protein from bulk solution to a solid/liquid interface may incur: i) a change in its conformation, ii) relaxation and partial desorption, iii) reorientation and alignment as a function of surface coverage. The protein layer may also undergo transition from a monolayer to a multilayer as the surface becomes saturated. Changes in orientation and surface coverage were seen for random adsorption of FN fragments, wherein the adsorption model was analogous to the surface pressure area isotherm of surfactants. Concomitant structural changes were also observed during the random adsorption of FIII9’10 to silica, wherein a distorted, non-native conformation was observed to be associated with the aromatic residues being held in a more ridged state. However, in order to better define the relationship between cell behavior and a 2-D ligand display, it is necessary to characterise the ligand pattern and density that is interrogated by the cell surface integrin receptors. This requires an engineering approach in which ligands are tethered in a controlled manner to the surface. Such approaches have been described for RGD-peptides at least, with the development of comb-like polymers and self-assembling monolayers (SAMs) permitting the calculation of ligand densities and ligand clustering.
Application of SAMs to larger protein domains remains unclear since the cross-linking of proteins to the gold/alkanethiolate brush border appears to leave significant proportions of the immobilised protein non-specifically adsorbed. Similarly, one report for cross-linking FIII7-10 to adsorbed BSA did not address random ligand orientation or adsorption-induced unfolding. A carrier or tether facilitating uniform ligand orientation upon immobilisation is therefore required. Such tethers have been described for FN fragments, using either a unique C-terminal cysteine residue which can be specifically biotinlylated for controlled binding to a streptavidin surface (Fig. 6), or covalent conjugation through a synthetic protocol. With respect to the latter, clinical-grade titanium implants grafted with a non-fouling polymer coating, functionalised with a controlled density (0.9 pmol/cm2) of FIII7-10 have been tested
7. Stem cell behavior and substrate ‘stiffness’
An important outcome of the studies on ECM-directed control of cell behaviour will be improvements in our ability to grow mammalian embryonic stem (ES) cells in culture systems completely free of animal material. Given the therapeutic potential for cultured cells, development of such animal free systems is a major imperative. This is most pressing in the field of stem cell biology where human ES (hES) cells provide a potentially novel source for the derivation of transplantable tissue specific cell types. ES cells were initially developed from the inner cell mass of the d3.5 murine blastocyst and have been demonstrated to be capable of contributing to all three germ layers of the developing embryo. These murine ES (mES) cells can differentiate
mature cell types such as haemopoietic cells, cardiac muscle cells, endothelial cells and neurons. Isolated hES cells have also been shown to contribute to all three germ layers. The ability of these cells to differentiate
The nature of the ECM is also known to regulate ES cell behavior. For example, mES cells cultured on type I and type IV collagen or poly-D-lysine retained an undifferentiated state but when cultured on laminin or FN displayed altered morphology and downregulated signal transducer and activator of transcription 3, which maintains ES cell self-renewal. Inhibition of integrin-fibronectin binding prevented the observed differentiation response and in serum-replacement media the mES cells expressed integrin subtypes specific for laminin and fibronectin, but not for collagen. It is therefore apparent that the integrin subtype specific for fibronectin, namely integrin α5β1, is likely to play a role in mES cell behavior upon adhesion to ECM. As for stromal and fibroblast cells (discussed above), mES cells showed clear morphological responses to clustered versus monomeric FN fragments. The mES colonies appeared disperse with a spread cell morphology on dimeric FIII9’10, unless subdued back to a tight morphology with increasing concentrations of leukaemia inhibitory factor (LIF) (Fig. 8). In the presence of LIF, mES cells adherent to the FIII9'10-dimer also showed transient upregulation of Oct-4, the mesodermal transcription factor, Brachyury, and the ectodermal marker, Nestin. However, dual upregulation of Nanog maintained the mES cells in a pluripotent state, confirmed by alkaline phosphatase staining. Since the mES cells grow as dispersed colonies in a monolayer, FIII9'10-dimer could have application as an alternative substrate on which to study ES cell differentiation in 2-D.
However, cellular responses to ECM signals are context-dependent: ECM signals presented in 3-D differ from those presented in 2-D. For example, focal adhesion formation during cell-ECM adhesion is mechanistically different in naturally derived hydrogels when compared to protein-coated tissue culture polystyrene substrates. These context dependent changes are due to cell-substrate mechanics, involving local forces generated by the cell during spreading and primary (tissue) cell sensing of the synthetic substrate stiffness, or local variations of ECM elasticity
This will involve developing hydrogels containing a bioinert polymer that is furnished with spatially defined ECM-derived ligands, while avoiding non-specific interactions with other molecules. A defined synthetic biomaterial is preferred over ‘naturally based’ hydrogels such as Matrigel and collagens which are biochemically complex (to tune), variable and ill-defined, and therefore make interpretation of cellular responses more complex. Hydrogels are particularly promising because they do not only have a high water content to promote cell viability, but they are structurally and mechanically similar to the native ECM of many tissues. The polymers forming the hydrogel structure must be bioinert, rather than having inherent cell adhesive activity such as gels of fibrin or hyaluronan, in order to test the capacity of the gels to support a specific cell function. Bioinert polymers such as alginate or poly(ethylene glycol) must therefore be covalently cross-linked with ECM-derived ligands to physically resist cell traction forces and prevent ligand leaching.
The role of integrins in determining self-renewal versus differentiation has been investigated using mES cells embedded in hydrogels functionalised with three peptides selective for integrins α5β1, αvβ5, α6β1 and α9β1. Broadly, maintenance of mES cell self-renewal and pluripotency, with down-regulation of differentiation-related genes, required multiple integrin subtype binding. It has also been shown that hES cells adherent to Matrigel predominantly expressed integrin α6, αvβ3, α2β1 and (particularly) β1. These synthetic gels were functionalised with three peptides engaging integrins αvβ3, α5β1 and α6β1. As for mES cells, maintenance of self-renewal required multiple integrin engagement, with hydrogels functionalised with one peptide supporting only hES cell adhesion and pluripotency. Integrin-mediated adhesion has also been shown to regulate the assembly of single-cell suspensions of hES cells into pluripotent hES cell colonies in the absence of feeder cells or added cytokines.
A degree of control over cellular processes is desired for regenerative medicine and to this end, FN fragments (FIII9’10) designed to specifically target integrin α5β1 were investigated in the context of osteogenic differentiation. When FIII9’10 was coated onto surfaces, human mesenchymal stem cells displayed increased adhesion, proliferation and spreading compared to the (conformationally less stable) wild type FIII9-10. Interestingly, selective inhibition of α5β1 was shown to reduce proliferation of cells on FIII9’10 and FIII9-10 but not on FN or FIII10, suggesting a degree of specificity. Furthermore, stronger osteoinduction potential was exhibited by the FN fragments containing FIII9 compared with full length FN and domain FIII10. The lower osteoinductive effects shown on FIII10 would be expected because it does not include the PHSRN synergy site which is required for full α5β1 integrin binding. FIII9’10 appears to better mimic full length FN with the addition of improved osteoinductive effects mediated through the α5β1 integrin, and this may prove useful for the further development controlled cell systems.
It is highly desirable to control ES cell proliferation and differentiation on 2-D and 3-D substrates in order to generate clinically useful tissues for regenerative medicine. To achieve this it will be necessary to recapitulate the ES cell niche