Growth factors in the initial stage of bone formation, analysis of their expression in chondrocytes from epiphyseal cartilage of rat costochondral junction
Abstract
Introduction. In endochondral ossification septoclasts and osteoclasts (also called chondroclasts) release growth factors deposited in non-calcified and calcified zones of the growth plate. They stimulate, within the metaphysis, initial stages of the bone formation. We have recently reported quantitation of several growth factors in calcified cartilage from calf costochondral junction. Data from the analogous human cartilage could possibly help to choose efficient combinations of growth factors for clinical applications, but the amount of the calcified cartilage needed for analysis of numerous growth factors would be difficult to collect. The estimation of growth factors expression in endochondral chondrocytes may, indirectly, indicate which of them play a leading role in the stimulation of osteoprogenitor cells in metaphysis. To test this hypothesis, we used rat chondrocytes to evaluate mRNA levels of several growth factors. Materials and methods. Chondrocytes were isolated from proliferative and hypertrophic zones of the epiphyseal cartilage forming costochondral junctions of inbred Lewis rats. The total RNA was isolated from chondrocytes and the level of mRNA for bone morphogenetic proteins 1-7 (BMP-1-7), vascular endothelial growth factor A (VEGF-A), basic fibroblast growth factor (bFGF), growth/differentiation factor 5 (GDF-5), NEL-like protein 1 (NELL-1), transforming growth factor beta 1 (TGF-b1), mesencephalic astrocyte-derived neurotrophic factor (MANF), connective tissue growth factor (CTGF), osteoclast-stimulating factor 1 (OSTF-1) and insulin-like growth factor 1 (IGF-1) was evaluated using real-time PCR method. Results. All studied factors were expressed. The highest level of mRNA was detected for CTGF, MANF, VEGF-A and TGF-b1. Expression was also quite high for BMP-1, BMP-2, BMP-5, BMP-6, BMP-7, IGF-1, GDF-5 and OSTF-1. Very low level of mRNA was detected for BMP-3, BMP-4 and NELL-1.
Conclusions. Chondrocytes from the proliferative and hypertrophic zones of the growth plate produce factors involved in the cartilage metabolism and bone formation. The determination of these growth factors in humans could help to choose their optimal composition necessary for stimulation of bone formation in clinical practice. In rat the best stimulation of bone formation would presumably be achieved with a mixture of BMP-2, BMP-5, BMP-6 and BMP-7.
Keywords: ratepiphyseal cartilagecostochondral junctionbone formationgrowth factorsqPCR
References
- Adams SL, Cohen AJ, Lassová L. Integration of signaling pathways regulating chondrocyte differentiation during endochondral bone formation. J Cell Physiol. 2007; 213(3): 635–641.
- Amizuka N, Hasegawa T, Oda K, et al. Histology of epiphyseal cartilage calcification and endochondral ossification. Front Biosci (Elite Ed). 2012; 4: 2085–2100.
- Patil AS, Sable RB, Kothari RM. Occurrence, biochemical profile of vascular endothelial growth factor (VEGF) isoforms and their functions in endochondral ossification. J Cell Physiol. 2012; 227(4): 1298–1308.
- Burdan F, Szumiło J, Korobowicz A, et al. Morphology and physiology of the epiphyseal growth plate. Folia Histochem Cytobiol. 2009; 47(1): 5–16.
- Brochhausen C, Lehmann M, Halstenberg S, et al. Signalling molecules and growth factors for tissue engineering of cartilage-what can we learn from the growth plate? J Tissue Eng Regen Med. 2009; 3(6): 416–429.
- Mackie EJ, Tatarczuch L, Mirams M. The skeleton: a multi-functional complex organ: the growth plate chondrocyte and endochondral ossification. J Endocrinol. 2011; 211(2): 109–121.
- Marino R. Growth plate biology: new insights. Curr Opin Endocrinol Diabetes Obes. 2011; 18(1): 9–13.
- Lui JC, Nilsson O, Baron J. Recent research on the growth plate: Recent insights into the regulation of the growth plate. J Mol Endocrinol. 2014; 53(1): T1–T9.
- Bonucci E. Fine structure of early cartilage calcification. J Ultrastruct Res. 1967; 20(1): 33–50.
- Ali SY, Sajdera SW, Anderson HC. Isolation and characterization of calcifying matrix vesicles from epiphyseal cartilage. Proc Natl Acad Sci U S A. 1970; 67(3): 1513–1520.
- Anderson H. VESICLES ASSOCIATED WITH CALCIFICATION IN THE MATRIX OF EPIPHYSEAL CARTILAGE. J Cell Biol. 1969; 41(1): 59–72.
- Jaroszewicz J, Bazarnik P, Osiecka-Iwan A, et al. From Matrix Vesicles to Miniature Rocks: Evolution of Calcium Deposits in Calf Costochondral Junctions. Cartilage. 2020 [Epub ahead of print]: 1947603520941225.
- Anderson HC, Hodges PT, Aguilera XM, et al. Bone morphogenetic protein (BMP) localization in developing human and rat growth plate, metaphysis, epiphysis, and articular cartilage. J Histochem Cytochem. 2000; 48(11): 1493–1502.
- Nahar NN, Missana LR, Garimella R, et al. Matrix vesicles are carriers of bone morphogenetic proteins (BMPs), vascular endothelial growth factor (VEGF), and noncollagenous matrix proteins. J Bone Miner Metab. 2008; 26(5): 514–519.
- Enomoto-Iwamoto M, Iwamoto M, Mukudai Y, et al. Bone morphogenetic protein signaling is required for maintenance of differentiated phenotype, control of proliferation, and hypertrophy in chondrocytes. J Cell Biol. 1998; 140(2): 409–418.
- Tsumaki N, Yoshikawa H. The role of bone morphogenetic proteins in endochondral bone formation. Cytokine & Growth Factor Reviews. 2005; 16(3): 279–285.
- Salazar VS, Gamer LW, Rosen V. BMP signalling in skeletal development, disease and repair. Nat Rev Endocrinol. 2016; 12(4): 203–221.
- Nilsson O, Parker EA, Hegde A, et al. Gradients in bone morphogenetic protein-related gene expression across the growth plate. J Endocrinol. 2007; 193(1): 75–84.
- Snelling SJB, Hulley PA, Loughlin J. BMP5 activates multiple signaling pathways and promotes chondrogenic differentiation in the ATDC5 growth plate model. Growth Factors. 2010; 28(4): 268–279.
- Horner A, Bishop NJ, Bord S, et al. Immunolocalisation of vascular endothelial growth factor (VEGF) in human neonatal growth plate cartilage. J Anat. 1999; 194 ( Pt 4): 519–524.
- Carlevaro MF, Cermelli S, Cancedda R, et al. Vascular endothelial growth factor (VEGF) in cartilage neovascularization and chondrocyte differentiation: auto-paracrine role during endochondral bone formation. J Cell Sci. 2000; 113 ( Pt 1): 59–69.
- Engsig MT, Chen QJ, Vu TH, et al. Matrix metalloproteinase 9 and vascular endothelial growth factor are essential for osteoclast recruitment into developing long bones. J Cell Biol. 2000; 151(4): 879–889.
- Ortega N, Wang Ke, Ferrara N, et al. Complementary interplay between matrix metalloproteinase-9, vascular endothelial growth factor and osteoclast function drives endochondral bone formation. Dis Model Mech. 2010; 3(3-4): 224–235.
- Yang YQ, Tan YY, Wong R, et al. The role of vascular endothelial growth factor in ossification. Int J Oral Sci. 2012; 4(2): 64–68.
- Kerkhofs J, Roberts SJ, Luyten FP, et al. Relating the chondrocyte gene network to growth plate morphology: from genes to phenotype. PLoS One. 2012; 7(4): e34729.
- Li Bo, Wang H, Qiu G, et al. Synergistic Effects of Vascular Endothelial Growth Factor on Bone Morphogenetic Proteins Induced Bone Formation In Vivo: Influencing Factors and Future Research Directions. Biomed Res Int. 2016; 2016: 2869572.
- Iwan A, Moskalewski S, Hyc A. Growth factor profile in calcified cartilage from the metaphysis of a calf costochondral junction, the site of initial bone formation. Biomed Rep. 2021; 14(6): 54.
- BRIGHTON C, SUGIOKA Y, HUNT R. Cytoplasmic Structures of Epiphyseal Plate Chondrocytes. J Bone Joint Surg. 1973; 55(4): 771–784.
- Byard RW, Foster BK, Byers S. Immunohistochemical characterisation of the costochondral junction in SIDS. J Clin Pathol. 1993; 46(2): 108–112.
- Clark CC, Tolin BS, Brighton CT. The effect of oxygen tension on proteoglycan synthesis and aggregation in mammalian growth plate chondrocytes. J Orthop Res. 1991; 9(4): 477–484.
- Wozney J. Overview of Bone Morphogenetic Proteins. Spine. 2002; 27(Supplement): S2–S8.
- Termaat MF, Den Boer FC, Bakker FC, et al. Bone morphogenetic proteins. Development and clinical efficacy in the treatment of fractures and bone defects. J Bone Joint Surg Am. 2005; 87(6): 1367–1378.
- Vukicevic S, Oppermann H, Verbanac D, et al. The clinical use of bone morphogenetic proteins revisited: a novel biocompatible carrier device OSTEOGROW for bone healing. Int Orthop. 2014; 38(3): 635–647.
- James AW, LaChaud G, Shen J, et al. A Review of the Clinical Side Effects of Bone Morphogenetic Protein-2. Tissue Eng Part B Rev. 2016; 22(4): 284–297.
- Epstein NE. Basic science and spine literature document bone morphogenetic protein increases cancer risk. Surg Neurol Int. 2014; 5(Suppl 15): S552–S560.
- Seeherman H, Wozney JM. Delivery of bone morphogenetic proteins for orthopedic tissue regeneration. Cytokine Growth Factor Rev. 2005; 16(3): 329–345.
- Park SY, Kim KH, Kim S, et al. BMP-2 Gene Delivery-Based Bone Regeneration in Dentistry. Pharmaceutics. 2019; 11(8).
- Loozen LD, Kruyt MC, Kragten AHM, et al. BMP-2 gene delivery in cell-loaded and cell-free constructs for bone regeneration. PLoS One. 2019; 14(7): e0220028.
- Mumcuoglu D, Fahmy-Garcia S, Ridwan Y, et al. Injectable BMP-2 delivery system based on collagen-derived microspheres and alginate induced bone formation in a time- and dose-dependent manner. Eur Cell Mater. 2018; 35: 242–254.
- Maisani M, Sindhu KR, Fenelon M, et al. Prolonged delivery of BMP-2 by a non-polymer hydrogel for bone defect regeneration. Drug Deliv Transl Res. 2018; 8(1): 178–190.
- Marsell R, Einhorn TA. The biology of fracture healing. Injury. 2011; 42(6): 551–555.
- Academy of Medical Royal Colleges. Ethical issues in paediatric organ donation. UK Donation Ethics Committee (UKDEC) 2015:4. URL: https://www.aomrc.org.uk/wp-content/uploads/2016/04/Paediatric_organ_donation_position_0615-2.pdf.
- He T, Huang Y, Chak JC, et al. Recommendations for improving accuracy of gene expression data in bone and cartilage tissue engineering. Sci Rep. 2018; 8(1): 14874.
- Lopa S, Ceriani C, Cecchinato R, et al. Stability of housekeeping genes in human intervertebral disc, endplate and articular cartilage cells in multiple conditions for reliable transcriptional analysis. Eur Cell Mater. 2016; 31: 395–406.
- Han H, Liu L, Chen M, et al. The optimal compound reference genes for qRT-PCR analysis in the developing rat long bones under physiological conditions and prenatal dexamethasone exposure model. Reprod Toxicol. 2020; 98: 242–251.
- Arnott JA, Lambi AG, Mundy C, et al. The role of connective tissue growth factor (CTGF/CCN2) in skeletogenesis. Crit Rev Eukaryot Gene Expr. 2011; 21(1): 43–69.
- Ramazani Y, Knops N, Elmonem MA, et al. Connective tissue growth factor (CTGF) from basics to clinics. Matrix Biol. 2018; 68-69: 44–66.
- Bell PA, Dennis EP, Hartley CL, et al. Mesencephalic astrocyte-derived neurotropic factor is an important factor in chondrocyte ER homeostasis. Cell Stress Chaperones. 2019; 24(1): 159–173.
- Reddy S, Devlin R, Menaa C, et al. Isolation and characterization of a cDNA clone encoding a novel peptide (OSF) that enhances osteoclast formation and bone resorption. J Cell Physiol. 1998; 177(4): 636–645, doi: 10.1002/(SICI)1097-4652(199812)177:4<636::AID-JCP14>3.0.CO;2-H.
- Steiglitz BM, Ayala M, Narayanan K, et al. Bone morphogenetic protein-1/Tolloid-like proteinases process dentin matrix protein-1. J Biol Chem. 2004; 279(2): 980–986.
- Vadon-Le Goff S, Hulmes DJS, Moali C. BMP-1/tolloid-like proteinases synchronize matrix assembly with growth factor activation to promote morphogenesis and tissue remodeling. Matrix Biol. 2015; 44-46: 14–23.
- Mailhot G, Yang M, Mason-Savas A, et al. BMP-5 expression increases during chondrocyte differentiation in vivo and in vitro and promotes proliferation and cartilage matrix synthesis in primary chondrocyte cultures. J Cell Physiol. 2008; 214(1): 56–64.
- Ye F, Xu H, Yin H, et al. The role of BMP6 in the proliferation and differentiation of chicken cartilage cells. PLoS One. 2019; 14(7): e0204384.
- Yakar S, Werner H, Rosen CJ. Insulin-like growth factors: actions on the skeleton. J Mol Endocrinol. 2018; 61(1): T115–T137.
- Racine HL, Serrat MA. The Actions of IGF-1 in the Growth Plate and Its Role in Postnatal Bone Elongation. Curr Osteoporos Rep. 2020; 18(3): 210–227.
- Wozney JM, Rosen V. Bone morphogenetic protein and bone morphogenetic protein gene family in bone formation and repair. Clin Orthop Relat Res. 1998(346): 26–37.
- Wutzl A, Rauner M, Seemann R, et al. Bone morphogenetic proteins 2, 5, and 6 in combination stimulate osteoblasts but not osteoclasts in vitro. J Orthop Res. 2010; 28(11): 1431–1439.
- Zhou N, Li Qi, Lin X, et al. BMP2 induces chondrogenic differentiation, osteogenic differentiation and endochondral ossification in stem cells. Cell Tissue Res. 2016; 366(1): 101–111.
- Bahamonde M, Lyons K. BMP3: To Be or Not To Be a BMP. J Bone Joint Surg Am-American Volume. 2001; 83: S1-56–S1–62.
- Gamer LW, Cox K, Carlo JM, et al. Overexpression of BMP3 in the developing skeleton alters endochondral bone formation resulting in spontaneous rib fractures. Dev Dyn. 2009; 238(9): 2374–2381.
- Peng H, Wright V, Usas A, et al. Synergistic enhancement of bone formation and healing by stem cell-expressed VEGF and bone morphogenetic protein-4. J Clin Invest. 2002; 110(6): 751–759.
- Shum L, Wang X, Kane AA, et al. BMP4 promotes chondrocyte proliferation and hypertrophy in the endochondral cranial base. Int J Dev Biol 2003;47(6):423-431. .
- Gao X, Usas A, Lu A, et al. BMP2 is superior to BMP4 for promoting human muscle-derived stem cell-mediated bone regeneration in a critical-sized calvarial defect model. Cell Transplant. 2013; 22(12): 2393–2408.
- Chang SC, Hoang B, Thomas JT, et al. Cartilage-derived morphogenetic proteins. New members of the transforming growth factor-beta superfamily predominantly expressed in long bones during human embryonic development. J Biol Chem. 1994; 269(45): 28227–28234.
- Tsumaki N, Tanaka K, Arikawa-Hirasawa E, et al. Role of CDMP-1 in skeletal morphogenesis: promotion of mesenchymal cell recruitment and chondrocyte differentiation. J Cell Biol. 1999; 144(1): 161–173.
- Storm EE, Huynh TV, Copeland NG, et al. Limb alterations in brachypodism mice due to mutations in a new member of the TGF beta-superfamily. Nature. 1994; 368(6472): 639–643.
- Polinkovsky A, Robin NH, Thomas JT, et al. Mutations in CDMP1 cause autosomal dominant brachydactyly type C. Nat Genet. 1997; 17(1): 18–19.
- Zhang X, Zara J, Siu RK, et al. The role of NELL-1, a growth factor associated with craniosynostosis, in promoting bone regeneration. J Dent Res. 2010; 89(9): 865–878.
- Tanjaya J, Zhang Y, Lee S, et al. Efficacy of Intraperitoneal Administration of PEGylated NELL-1 for Bone Formation. Biores Open Access. 2016; 5(1): 159–170.
- James AW, Shen J, Tsuei R, et al. NELL-1 induces Sca-1+ mesenchymal progenitor cell expansion in models of bone maintenance and repair. JCI Insight. 2017; 2(12).
- Qi H, Kim JK, Ha P, et al. Inactivation of Nell-1 in Chondrocytes Significantly Impedes Appendicular Skeletogenesis. J Bone Miner Res. 2019; 34(3): 533–546.
- Chen G, Deng C, Li YP. TGF-β and BMP signaling in osteoblast differentiation and bone formation. Int J Biol Sci. 2012; 8(2): 272–288.
- Wu M, Chen G, Li YP. TGF-β and BMP signaling in osteoblast, skeletal development, and bone formation, homeostasis and disease. Bone Res. 2016; 4: 16009.
- Wezeman FH, Bollnow MR. Immunohistochemical localization of fibroblast growth factor-2 in normal and brachymorphic mouse tibial growth plate and articular cartilage. Histochem J. 1997; 29(6): 505–514.
- Nagai H, Tsukuda R, Mayahara H. Effects of basic fibroblast growth factor (bFGF) on bone formation in growing rats. Bone. 1995; 16(3): 367–373.
- Kusafuka K, Hiraki Y, Shukunami C, et al. Cartilage-specific matrix protein, chondromodulin-I (ChM-I), is a strong angio-inhibitor in endochondral ossification of human neonatal vertebral tissues in vivo: relationship with angiogenic factors in the cartilage. Acta Histochem. 2002; 104(2): 167–175.
- Gerber HP, Vu TH, Ryan AM, et al. VEGF couples hypertrophic cartilage remodeling, ossification and angiogenesis during endochondral bone formation. Nat Med. 1999; 5(6): 623–628.
- Nagao M, Hamilton JL, Kc R, et al. Vascular Endothelial Growth Factor in Cartilage Development and Osteoarthritis. Sci Rep. 2017; 7(1): 13027.
- Vadalà G, Russo F, Musumeci M, et al. Targeting VEGF-A in cartilage repair and regeneration: state of the art and perspectives. J Biol Regul Homeost Agents 2018;32(6 suppl. ):217-224. .
- Horner A, Kemp P, Summers C, et al. Expression and distribution of transforming growth factor-beta isoforms and their signaling receptors in growing human bone. Bone. 1998; 23(2): 95–102.