Literature DB >> 17306969

Chondrocyte hypertrophy can be induced by a cryptic sequence of type II collagen and is accompanied by the induction of MMP-13 and collagenase activity: implications for development and arthritis.

Elena V Tchetina1, Masahiko Kobayashi, Tadashi Yasuda, Tineke Meijers, Isabelle Pidoux, A Robin Poole.   

Abstract

The objective of this study was to determine whether a peptide of type II collagen which can induce collagenase activity can also induce chondrocyte terminal differentiation (hypertrophy) in articulate cartilage. Full depth explants of normal adult bovine articular cartilage were cultured with or without a 24 mer synthetic peptide of type II collagen (residues 195-218) (CB12-II). Peptide CB12-II lacks any RGD sequence and is derived from the CB12 fragment of type II collagen. Type II collagen cleavage by collagenase was measured by ELISA in cartilage and medium. Real-time RT-PCR was used to analyze gene expression of the chondrocyte hypertrophy markers COL10A1 and MMP-13. Immunostaining for anti-Ki67, anti-PCNA, (proliferation markers), type X collagen, cleavage of type II collagen by collagenases (hypertrophy markers) and TUNEL staining (hypertrophy and apoptosis markers) were used to detect progressive maturational stages of chondrocyte hypertrophy. At high but naturally occurring concentrations (10 microM and up) the collagen peptide CB12-II induced an increase in the expression of MMP-13 (24 h) and cleavage of type II collagen by collagenase in the mid zone (day 4) and also in the superficial zone (day 6). Furthermore the peptide induced an increase in proliferation on day 1 in the mid and deep zones extending to the superficial zone by day 4. There was also upregulation of COL10A1 expression at day 4 and of type X staining in the mid zone extending to the superficial zone by day 6. Apoptotic cell death was increased by day 4 in the lower deep zone and also in the superficial zone at day 7. The increase in apoptosis in the deep zone was also seen in controls. Our results show that the induction of collagenase activity by a cryptic peptide sequence of type II collagen, is accompanied by chondrocyte hypertrophy and associated with cellular and matrix changes. This induction occurs in the mid and superficial zones of previously healthy articular cartilage. This response of the chondrocyte to a cryptic sequence of denatured type II collagen may play a role in naturally occurring hypertrophy in endochondral ossification and in the development of cartilage pathology in osteoarthritis.

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Year:  2007        PMID: 17306969     DOI: 10.1016/j.matbio.2007.01.006

Source DB:  PubMed          Journal:  Matrix Biol        ISSN: 0945-053X            Impact factor:   11.583


  27 in total

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2.  Joint aging and chondrocyte cell death.

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3.  Roles of inflammatory and anabolic cytokines in cartilage metabolism: signals and multiple effectors converge upon MMP-13 regulation in osteoarthritis.

Authors:  Mary B Goldring; Miguel Otero; Darren A Plumb; Cecilia Dragomir; Marta Favero; Karim El Hachem; Ko Hashimoto; Helmtrud I Roach; Eleonora Olivotto; Rosa Maria Borzì; Kenneth B Marcu
Journal:  Eur Cell Mater       Date:  2011-02-24       Impact factor: 3.942

4.  Matrix metalloproteinase 13-deficient mice are resistant to osteoarthritic cartilage erosion but not chondrocyte hypertrophy or osteophyte development.

Authors:  C B Little; A Barai; D Burkhardt; S M Smith; A J Fosang; Z Werb; M Shah; E W Thompson
Journal:  Arthritis Rheum       Date:  2009-12

5.  Regulation of gene expression by PI3K in mouse growth plate chondrocytes.

Authors:  Veronica Ulici; Claudine G James; Katie D Hoenselaar; Frank Beier
Journal:  PLoS One       Date:  2010-01-25       Impact factor: 3.240

6.  Smurf2 induces degradation of GSK-3beta and upregulates beta-catenin in chondrocytes: a potential mechanism for Smurf2-induced degeneration of articular cartilage.

Authors:  Qiuqian Wu; Jason H Huang; Erik R Sampson; Kyung-O K Kim; Michael J Zuscik; Regis J O'Keefe; Di Chen; Randy N Rosier
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Review 7.  Stem cell- and scaffold-based tissue engineering approaches to osteochondral regenerative medicine.

Authors:  Sarah Sundelacruz; David L Kaplan
Journal:  Semin Cell Dev Biol       Date:  2009-08       Impact factor: 7.727

8.  Localization of the cis-enhancer element for mouse type X collagen expression in hypertrophic chondrocytes in vivo.

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Journal:  J Bone Miner Res       Date:  2009-06       Impact factor: 6.741

9.  Osteoblasts derived from osteophytes produce interleukin-6, interleukin-8, and matrix metalloproteinase-13 in osteoarthritis.

Authors:  Kei Sakao; Kenji A Takahashi; Yuji Arai; Masazumi Saito; Kuniaki Honjo; Nobuyuki Hiraoka; Hidetsugu Asada; Masaharu Shin-Ya; Jiro Imanishi; Osam Mazda; Toshikazu Kubo
Journal:  J Bone Miner Metab       Date:  2009-04-01       Impact factor: 2.626

10.  Mustn1 is expressed during chondrogenesis and is necessary for chondrocyte proliferation and differentiation in vitro.

Authors:  Robert P Gersch; Michael Hadjiargyrou
Journal:  Bone       Date:  2009-05-03       Impact factor: 4.398

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