Human PRL prohormone amino acid sequence (position 1–227) and mature PRL (position 29–227). The signal peptide is position 1-28 in the bold letters.
PRL gene-encoded prolactin is synthesized in the ribosome in the pituitary and then secretes into blood circulation to reach its target organ and exerts its biological roles, for example, involving in production, growth, development, immunoregulation, and metabolism. Multiple post-translational modifications and other unknown factors might be involved in this process to cause different prolactin proteoforms with differential isoelectric point (pI) and relative mass (Mr ). Pituitary adenomas are the common disease occurring in pituitary organ to affect the endocrine system. Two-dimensional gel electrophoresis (2DGE) was used to separate prolactin proteoforms according to their pI and Mr , followed by identification with Western blot and mass spectrometry (MS) analyses. Six prolactin proteoforms were identified in control pituitary tissues, and this prolactin proteoform pattern was significantly changed in different hormone subtypes of nonfunctional pituitary adenomas (NF−, LH+, FSH+, and LH+/FSH+) and prolactinomas (PRL+). Further, bioinformatics analysis revealed that different prolactin proteoforms might bind to different short- or long-PRL receptor-mediated signaling pathways. These findings clearly demonstrated that prolactin proteoform pattern existed in human pituitary and changed in different subtypes of pituitary adenomas. It is the scientific data to in-depth study prolactin functions, and to discover the prolactin proteoform biomarkers for PRL-related adenomas.
- prolactin proteoforms
- pituitary adenomas
- nonfunctional pituitary adenomas
Prolactin (PRL) is a multifunctional hormone which is synthesized and secreted by pituitary . Human PRL gene is located on chromosome 6 . The secretory mode of PRL is autocrine and paracrine , and the secretion of PRL is pulsating and circadian rhythm . The concentration of PRL in human serum has a certain reference range, and when its concentration is too high or too low, it will have a certain impact on the body. Dopamine can inhibit the secretion of PRL, and there are cases where dopamine is used to treat hyperprolactinemia . PRL’s biological functions include production, growth, development, immunoregulation, and metabolism [5, 6]. PRL can exert its biological functions only when it binds to its receptor and activates some signaling pathways . According to the concept of proteoforms, a protein is defined as a set of proteoforms, due to different splicing, post-translational modifications (PTMs), and even unknown factors. Each proteoform has its own specific isoelectric point (p
Recently 2DGE and MS have been recognized as high throughput and useful tool to study proteoforms [13, 14, 15]. 2DGE is able to separate each proteoform in the first dimension—isoelectric focusing (IEF) based on proteoform charge difference, and in the second dimension—sodium dodecyl sulfate polyacrylamide gel electrophoresis (SDS-PAGE) based on proteoform relative mass difference . Therefore, 2DGE achieves proteoform separation based on the difference in p
Pituitary adenomas are the common disease occurred in pituitary organ to severely impact on the human endocrine system. PRL is an important pituitary hormone. It has important scientific merit in clarification of PRL proteoform pattern changed in different subtypes of pituitary adenomas compared to control pituitaries. This book chapter focuses on the PRL proteoforms in human pituitary and investigates the PRL proteoform pattern alterations in pituitary adenomas relative to controls, with 2DGE and MS. These findings provide the scientific data to in-depth study the PRL functions and to discover PRL proteoform biomarker for PRL-related adenomas.
2.1 Pituitary tissue samples and preparation of protein samples
Eight human post-mortem control pituitary tissues, five PRL-positive prolactinoma tissues, three non-hormone expressed nonfunctional pituitary adenoma (NF-NFPA) tissues, three luteinizing hormone (LH)-positive NFPA tissues, three follicle-stimulating hormone (FSH)-positive NFPA tissues, and three LH/FSH-both positive NFPA tissues were used to extract proteins, with the previously described procedure [21, 22]. The extracted protein of each tissue sample was used for 2DGE and MS analysis.
A amount (70 μg) of proteins was diluted into 350 μL of protein sample buffer (7 mol/L urea, 2 mol/L thiourea, 40 g/L CHAPS, 100 mmol/L dithiothreitol (DTT), 5 mol/L immobilized pH gradient (IPG) buffer pH 3–10 NL, and a trace of bromophenol blue, followed by rehydration (18 h, 20°C) of precast IPG strips pH 3–10 NL (180 x 3 × 0.5 mm) in 18-cm IPG strip holder on an IPGphor instrument, and IEF (25°C) with parameters (Gradient 250 V and 1 h for 125 Vh, gradient at 1000 V and 1 h for 500 Vh, gradient at 8000 V and 1 h for 4000 Vh, step-and-hold at 8000 and 4 h for 32,000 Vh, step-and-hold at 500 V and 0.5 h for 250 Vh to achieve a total of 36,875 Vh). After IEF, the proteins on IPG strip were reduced (15 min) with DTT, and alkylated with iodoacetamide, followed by separation with 12% SDS-PAGE (250 × 215 × 1.0 mm) in an Ettan DALT II system (GE Healthcare, up to 12 gels at a time) with a constant voltage (250 V, 360 min). All 2DGE-arrayed proteins were stained with silver-staining , and then digitized and analyzed with Discovery Series PDQuest 2D Gel Analysis software [24, 25]. Each sample was performed for 3–5 times.
2.3 2DGE-based Western blot
The proteins in the 2D gel were partially transferred to a polyvinylidene fluoride (PVDF) membrane (0.8 mA/cm2 for 80 min) using Amersham Pharmacia Biotech Nova Blot semi-dry transfer instrument, followed by blocking (1 h, room temperature) with bovine serum albumin (BSA), incubation (1 h, room temperature) with rabbit anti-hPRL antibodies, incubation (1 h, room temperature) with goat anti-rabbit alkaline phosphatase conjugated IgG, and visualization with 5-bromo-4-chloro-3-indolyl phosphate. The detailed procedure was described previously .
2.4 In-gel digestion with trypsin and MS identification of PRL
The proteins in each Western blot-positive spot was performed in-gel digestion with trypsin, purification of tryptic peptides with ZipTipC18, followed by analysis with three types of MS instruments, including MALDI-TOF MS , LC-ESI-Q-IT MS , and MALDI-TOF-TOF MS . The detailed procedure was described previously [9, 24]. The obtained peptide mass fingerprint (PMF) and tandem mass spectrometry (MS/MS) data were used to search Swiss-Prot human database for protein determination and PTM analysis.
2.5 Bioinformatics and statistical analysis
The phosphorylation sites, O-glycosylation sites, and N-glycosylation sites in the PRL amino acid sequence were predicted with NetPhos 3.1 Server (http://www.cbs.dtu.dk/services/NetPhos) [26, 27], NetOGlyc 4.0 Server (http://www.cbs.dtu.dk/services/NetOGlyc) , and NetNGlyc 1.0 Server (http://www.cbs.dtu.dk/services/NetNGlyc) . The PRL proteoform pattern changes were tested with the Chi-square test among different subtypes of pituitary adenomas (p < 0.05).
3. Results and discussion
3.1 The amino acid sequences of human PRL prohormone and mature PRL
In human pituitary, the PRL prohormone is synthesized in the ribosome, with 227 amino acids (position 1–227; 25.9 kDa), containing a signal peptide (position 1–28) (Table 1), which was assigned with Swiss-Prot accession No. P01236. However, the mature human PRL only contains 199 amino acids (position 29–227; 22.9 kDa), which removed the signal peptide (position 1–28), and secreted into the circulation system to bind to its target organ for exerting PRL function.
3.2 PRL proteoform pattern in human pituitaries
The PRL proteoform pattern was found in human pituitaries. Qian et al.  found six PRL proteoforms with 2DGE in human pituitaries and then verified four of six PRL proteoforms with 2DGE-based Western blot in human pituitaries (Figures 1 and 2). The p
|Calc. [M + H]+||Position||Characteristic tryptic peptide sequence||Observed [M + H]+|
3.3 PRL proteoform changes in human pituitary adenomas compared to controls
The PRL proteoform pattern changed in different subtypes of pituitary adenomas compared to control pituitaries (Table 3). The ratio of each subtype of pituitary adenoma relative to control pituitaries was decreased or unchanged. The proportional ratio of six PRL proteoforms among five subtypes of pituitary adenomas was changed (Table 4 and Figure 5). In FSH+/LH+ and PRL+ pituitary adenomas, the proportion of PRL proteoform v1 is the largest. In FSH+ pituitary adenoma, the proportion of PRL proteoform v5 is the largest. The PRL proteoform changes suggest their scientific merit for clinical application.
|PRL proteoform no.||Swiss-Prot no.||Ratio (NF−: Con)||Ratio (FSH+/LH+: Con)||Ratio (FSH+: Con)||Ratio (LH+: Con)||Ratio (PRL: Con)|
|PRL proteoform||NF− (%)||FSH+/LH+ (%)||FSH+ (%)||LH+ (%)||PRL+ (%)|
3.4 Bioinformatics prediction of potential factors to form PRL proteoforms and pathway networks
PRL is a hormone which is secreted by pituitary gland. PRL has a variety of biological functions. Only when it reaches a specific target organ and binds to its receptor can it play its biological function (Figure 6). PRL can bind to short PRL receptor or long PRL receptor and then plays its biological functions. The long or short PRL receptors definitely bind to different PRL proteoforms. PRL proteoforms are definitely derived from a PRL gene undergoing splicing, transcription, translation, PTMs, translocation/re-distribution, and interaction with other molecules, etc. Therefore, phosphorylation sites in hPRL (position 1–227) were predicted with NetPhos 3.1 Server with a score more than 0.5. It obtained 22 statistically significantly phosphorylation sites in hPRL (position 1–227). N-glycosylation sites in hPRL (position 1–227) were predicted with NetNGlyc 1.0 Server with score more than 0.5. It obtained 10 statistically significant N-glycosylation sites in hPRL (position 1–227). O-glycosylation sites in hPRL (position 1–227) were predicted with NetOGlyc 4.0 Server with score more than 0.5. It obtained six statistically significant O-glycosylation sites in hPRL (position 1–227). These data suggest that PTMs such as phosphorylation and glycosylation might be the important reason to cause the PRL proteoforms.
3.5 Potential clinical application of PRL proteoform pattern
Prolactin synthesized in the ribosome in the pituitary secretes into blood circulation to reach its target organ and exert its biological roles, which is closely associated with multiple physiological and pathological processes, including pituitary adenomas. This study found six PRL proteoforms with different with differential isoelectric point (p
Six PRL proteoforms were identified in human pituitary tissue with 2DGE and MS analyses, and four of six PRL proteoforms were validated with 2DGE-based Western blot, MS, and MS/MS analyses. There were significant differences in PRL proteoform pattern among five different subtypes of pituitary adenomas (LH+, NF−, FSH+, FSH+/LH+, and PRL+) (P < 0.05). Moreover, MS analysis revealed that six PRL proteoforms are PRL prohormone. PRL proteoforms might be derived from PTMs such as phosphorylation, deamidation, and glycosylation. Further, different PRL proteoforms might bind to different PRL receptors to produce different physiological functions. These findings provide scientific basis for in-depth understanding of pituitary adenomas, and help develop biomarkers for treatment of pituitary adenoma patients. The serum PRL proteoform pattern has important clinical application value for prediction, diagnosis, and prognostic assessment of pituitary adenomas.
The authors acknowledge the financial supports from the Hunan Provincial Hundred Talent Plan (to X.Z.), National Natural Science Foundation of China (Grant No. 81572278 and 81272798 to X.Z.), China “863” Plan Project (Grant No. 2014AA020610-1 to X.Z.), the Hunan Provincial Natural Science Foundation of China (Grant No. 14JJ7008 to X.Z.), and the Xiangya Hospital Funds for Talent Introduction (to X.Z.).
Conflict of interest
The authors declare that they have no financial and personal relationships with other people or organizations.
X.Z. conceived the concept, designed the manuscript, wrote and critically revised the manuscript, coordinated, and was responsible for the correspondence work and financial support. Q.S. participated in the literature analysis, data analysis, prepared figures, and wrote partial manuscript.
|IPG||immobilized pH gradient|
|SDS-PAGE||sodium dodecyl sulfate polyacrylamide gel electrophoresis|
|2DGE||two-dimensional gel electrophoresis|