Regulation of articular chondrocyte proliferation and differentiation by indian hedgehog and parathyroid hormone–related protein in mice
Xuesong Chen
Yale University School of Medicine, New Haven, Connecticut
Search for more papers by this authorCarolyn M. Macica
Yale University School of Medicine, New Haven, Connecticut
Search for more papers by this authorAli Nasiri
Yale University School of Medicine, New Haven, Connecticut
Search for more papers by this authorCorresponding Author
Arthur E. Broadus
Yale University School of Medicine, New Haven, Connecticut
Department of Internal Medicine, Yale University School of Medicine, Section of Endocrinology, 333 Cedar Street, New Haven, CT 06520-8020Search for more papers by this authorXuesong Chen
Yale University School of Medicine, New Haven, Connecticut
Search for more papers by this authorCarolyn M. Macica
Yale University School of Medicine, New Haven, Connecticut
Search for more papers by this authorAli Nasiri
Yale University School of Medicine, New Haven, Connecticut
Search for more papers by this authorCorresponding Author
Arthur E. Broadus
Yale University School of Medicine, New Haven, Connecticut
Department of Internal Medicine, Yale University School of Medicine, Section of Endocrinology, 333 Cedar Street, New Haven, CT 06520-8020Search for more papers by this authorAbstract
Objective
Chondrocytes of the epiphyseal growth zone are regulated by the Indian hedgehog (IHH)–parathyroid hormone–related protein (PTHrP) axis. In weight-bearing joints, this growth zone comes to be subdivided by the secondary ossification center into distinct articular and growth cartilage structures. The purpose of this study was to explore the cells of origin, localization, regulation of expression, and putative functions of IHH and PTHrP in articular cartilage in the mouse.
Methods
We assessed IHH and PTHrP expression in an allelic PTHrP-LacZ–knockin mouse and several versions of PTHrP-null mice. Selected joints were unloaded surgically to examine load-induction of PTHrP and IHH.
Results
The embryonic growth zone appears to serve as the source of PTHrP-expressing proliferative chondrocytes that populate both the forming articular cartilage and growth plate structures. In articular cartilage, these cells take the form of articular chondrocytes in the midzone. In PTHrP-knockout mice, mineralizing chondrocytes encroach upon developing articular cartilage but appear to be prevented from mineralizing the joint space by IHH-driven surface chondrocyte proliferation. In growing and adult mice, PTHrP expression in articular chondrocytes is load-induced, and unloading is associated with rapid changes in PTHrP expression and articular chondrocyte differentiation.
Conclusion
We conclude that the IHH–PTHrP axis participates in the maintenance of articular cartilage. Dysregulation of this system might contribute to the pathogenesis of arthritis.
REFERENCES
- 1 Kronenberg HM. Developmental regulation of the growth plate. Nature 2003; 423: 332–6.
- 2 Vortkamp A, Lee K, Lanske B, Segre GV, Kronenberg HM, Tabin CJ. Regulation of rate of cartilage differentiation by Indian hedgehog and PTH-related protein. Science 1996; 273: 613–22.
- 3 Niswander L. Interplay between the molecular signals that control vertebrate limb development. Int J Dev Biol 2002; 46: 877–81.
- 4 Long F, Zhang XM, Karp S, Yang Y, McMahon AP. Genetic manipulation of hedgehog signaling in the endochondral skeleton reveals a direct role in the regulation of chondrocyte proliferation. Development 2001; 128: 5099–108.
- 5 Kobayashi T, Soegiarto DW, Yang Y, Lanske B, Schipani E, McMahon AP, et al. Indian hedgehog stimulates periarticular chondrocyte differentiation to regulate growth plate length independently of PTHrP. J Clin Invest 2005; 115: 1734–42.
- 6 Shubin NH. Origin of evolutionary novelty: examples from limbs. J Morphol 2002; 252: 15–28.
- 7 Shubin NH, Daeschler EB, Jenkins FA Jr. The pectoral fin of Tiktaalik roseae and the origin of the tetrapod limb. Nature 2006; 440: 764–71.
- 8 Haines EW. The evolution of epiphyses and of endochondral bone. Biol Rev 1942; 17: 267–91.
- 9 Reno PL, McBurney DL, Lovejoy CO, Horton WE Jr. Ossification of the mouse metatarsal: differentiation and proliferation in the presence/absence of a defined growth plate. Anat Rec A Discov Mol Cell Evol Biol 2006; 288: 104–18.
- 10 Haines RW. Eudiathrodial joints in fishes. J Anat 1942; 77 (Pt 1): 12–9.
- 11 Chen X, Macica CM, Dreyer BE, Hammond VE, Hens JR, Philbrick WM, et al. Initial characterization of PTH-related protein gene-driven lacZ expression in the mouse. J Bone Miner Res 2006; 20: 113–23.
- 12 Chen X, Macica CM, Nasiri A, Judex S, Broadus AE. Mechanical regulation of PTHrP expression in entheses. Bone 2007; 41: 752–9.
- 13 Broadus AE, Macica CM, Chen X. The PTHrP functional domain is at the gates of endochondral bones. Ann N Y Acad Sci 2007; 1116: 65–81.
- 14 Karaplis AC, Luz A, Glowacki J, Bronson RJ, Tybolewicz VL, Kronenberg HM, et al. Lethal skeletal dysplasia from targeted disruption of the parathyroid hormone-related peptide gene. Genes Dev 1994; 8: 277–89.
- 15 Jiang XI, Kalajzic Z, Maye P, Braut A, Bellizzi J, Mina M, et al. Histological analysis of GFP expression in murine bone. J Histochem Cytochem 2005; 53: 593–602.
- 16 Young DC, Kinsley SD, Ryan KA, Dutko FJ. Selective inactivation of eukaryotic β-galactosidase in assays for inhibitors of HIV-1 TAT using bacterial β-galactosidase as a reporter enzyme. Anal Biochem 1993; 215: 24–39.
- 17 Philbrick WM, Dreyer BE, Nakchbandi IA, Karaplis AC. Parathyroid hormone-related protein is required for tooth eruption. Proc Natl Acad Sci U S A 1998; 95: 11846–51.
- 18 Nolte T, Kaufmann W, Schorsch F, Soames T, Weber E. Standardized assessment of cell proliferation: the approach of the RITA-CEPA working group. Exp Toxicol Pathol 2005; 57: 91–103.
- 19 Kember NF. Comparative patterns of cell division in epiphyseal cartilage plates in the rat. J Anat 1972; 111: 137–42.
- 20 Storm EE, Huynh TV, Copeland NG, Jenkins NA, Kingsley DM, Lee SJ. Limb alterations in brachypodism mice due to mutations in a new member of the TGFβ-superfamily. Nature 1994; 368: 639–43.
- 21 Brunet LJ, McMahon JA, McMahon AP, Harland RM. Noggin, cartilage morphogenesis, and joint formation in the mammalian skeleton. Science 1998; 280: 1455–7.
- 22 Pacifici M, Koyama E, Iwamoto M. Mechanisms of synovial joint and articular cartilage formation: recent advances, but many lingering mysteries. Birth Defects Res C Embryo Today 2005; 75: 237–48.
- 23 Lanske B, Karaplis AC, Lee K, Luz A, Vortkamp A, Pirro A, et al. PTH/PTHrP receptor in early development and Indian hedgehog-regulated bone growth. Science 1996; 273: 613–22.
- 24 Reno PL, Horton WE Jr, Elsey RM, Lovejoy CO. Growth plate formation and development in alligator and mouse metapodials: evolutionary and functional implications. J Exp Zoolog B Mol Dev Evol 2007; 308: 283–96.
- 25 Chen X, Macica CM, Ng KW, Broadus E. Stretch-induced PTH-related protein gene expression in osteoblasts. J Bone Miner Res 2005; 20: 1454–61.
- 26
Clemens TL,
Broadus AE.
Physiologic actions of PTH and PTHrP. IV. Vascular, cardiovascular, and neurologic actions. In:
JP Bilezikian, editor.
The parathyroids.
2nd ed.
New York:
Academic Press;
2001. p
261–74.
10.1016/B978-012098651-4/50018-3 Google Scholar
- 27 Tanaka N, Ohno S, Honda K, Tanimoto K, Doi T, Ohno-Nakahara M, et al. Cyclic mechanical strain regulates the PTHrP expression in cultured chondrocytes via activation of the Ca2+ channel. J Dent Res 2005; 84: 64–8.
- 28 O'Connor KM. Unweighting accelerates tidemark advancement in articular cartilage at the knee joint of rats. J Bone Miner Res 1997; 12: 580–9.
- 29 Brandt KD. Response of joint structures to inactivity and to reloading after immobilization. Arthritis Rheum 2003; 49: 267–71.
- 30 Carter DR, Beaupre GS, Wong M, Smith RL, Andriacchi TP, Schurman DJ. The mechanobiology of articular cartilage development and degeneration. Clin Orthop Relat Res 2004; 427 Suppl: S69–77.
- 31 Wu QQ, Zhang Y, Chen Q. Indian hedgehog is an essential component of mechanotransduction complex to stimulate chondrocyte proliferation. J Biol Chem 2001; 276: 35290–6.
- 32 Tang GH, Rabie AB, Hagg U. Indian hedgehog: a mechanotransduction mediator in condylar cartilage. J Dent Res 2004; 83: 434–8.
- 33 Hoshino A, Wallace WA. Impact-absorbing properties of the human knee. J Bone Joint Surg Br 1987; 69: 807–11.
- 34 Edwards CJ, Francis-West PH. Bone morphogenetic proteins in the development and healing of synovial joints. Semin Arthritis Rheum 2001; 31: 33–42.
- 35 Hyde G, Dover S, Aszodi A, Wallis GA, Boot-Handford RP. Lineage tracing using matrilin-1 gene expression reveals that articular chondrocytes exist as the joint interzone forms. Dev Biol 2007; 304: 825–33.
- 36 Koyama E, Shibukawa Y, Nagayama M, Sugito H, Young B, Yuasa T, et al. A distinct cohort of progenitor cells participates in synovial joint and articular cartilage formation during mouse limb skeletogenesis. Dev Biol 2008; 316: 62–73.
- 37 Burton DW, Foster M, Johnson KA, Hiramoto M, Deftos LJ, Terkeltaub R. Chondrocyte calcium-sensing receptor expression is up-regulated in early guinea pig knee osteoarthritis and modulates PTHrP, MMP-13, and TIMP-3 expression. Osteoarthritis Cartilage 2005; 13: 395–404.
- 38 Semevolos SA, Nixon AJ, Fortier LA, Strassheim ML, Haupt J. Age-related expression of molecular regulators of hypertrophy and maturation in articular cartilage. J Orthop Res 2006; 24: 1773–81.
- 39 Rabie AB, Tang GH, Xiong H, Hagg U. PTHrP regulates chondrocyte maturation in condylar cartilage. J Dent Res 2003; 82: 627–31.
- 40 Thiede MA, Daifotis AG, Weir EC, Brines ML, Burtis WJ, Ikeda K, et al. Intrauterine occupancy controls expression of the parathyroid hormone-related peptide gene in preterm rat myometrium. Proc Natl Acad Sci U S A 1990; 87: 6969–73.
- 41 Alvarez J, Sohn P, Zeng X, Doetschman T, Robbins DJ, Serra R. TGFβ2 mediates the effects of hedgehog on hypertrophic differentiation and PTHrP expression. Development 2002; 129: 1913–24.
- 42 Ho AM, Johnson MD, Kingsley DM. Role of the mouse ank gene in control of tissue calcification and arthritis. Science 2000; 289: 265–70.
- 43 Zhang Y, Brown MA, Peach C, Russell G, Wordsworth BP. Investigation of the role of ENPP1 and TNAP genes in chondrocalcinosis. Rheumatology (Oxford) 2007; 46: 586–9.
- 44 Goldring MB. The role of the chondrocyte in osteoarthritis [review]. Arthritis Rheum 2000; 43: 1916–26.
- 45 Sandell LJ, Aigner T. Articular cartilage and changes in arthritis. An introduction: cell biology of osteoarthritis. Arthritis Res 2001; 3: 107–13.
- 46 Drissi H, Zuscik M, Rosier R, O'Keefe R. Transcriptional regulation of chondrocyte maturation: potential involvement of transcription factors in OA pathogenesis. Mol Aspects Med 2005; 26: 169–79.