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II型胶原蛋白的隐蔽序列可诱导软骨细胞肥大,并伴有MMP-13的诱导和胶原酶活性:对发育和关节炎的影响。

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.

作者信息

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

机构信息

Joint Diseases Laboratory, Shriners Hospitals for Children and Department of Surgery, McGill University, Montreal, Quebec, Canada.

出版信息

Matrix Biol. 2007 May;26(4):247-58. doi: 10.1016/j.matbio.2007.01.006. Epub 2007 Jan 19.

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.

摘要

本研究的目的是确定一种可诱导胶原酶活性的II型胶原蛋白肽是否也能诱导关节软骨中的软骨细胞终末分化(肥大)。将正常成年牛关节软骨的全层外植体在添加或不添加II型胶原蛋白(残基195 - 218)的24聚体合成肽(CB12-II)的情况下进行培养。肽CB12-II缺乏任何RGD序列,且源自II型胶原蛋白的CB12片段。通过ELISA检测软骨和培养基中胶原酶对II型胶原蛋白的切割情况。使用实时RT-PCR分析软骨细胞肥大标志物COL10A1和MMP-13的基因表达。通过抗Ki67、抗PCNA(增殖标志物)、X型胶原蛋白免疫染色、胶原酶对II型胶原蛋白的切割(肥大标志物)以及TUNEL染色(肥大和凋亡标志物)来检测软骨细胞肥大的渐进成熟阶段。在高浓度但自然存在的浓度(10 microM及以上)下,胶原肽CB12-II在中层区域(第4天)和表层区域(第6天)诱导MMP-13表达增加(24小时)以及胶原酶对II型胶原蛋白的切割增加。此外,该肽在第1天诱导中层和深层区域的增殖增加,并在第4天扩展至表层区域。在第4天COL10A1表达上调,在第6天中层区域至表层区域的X型染色上调。在第4天深层下部区域以及第7天表层区域的凋亡细胞死亡增加。在对照组中也观察到深层区域凋亡增加。我们的结果表明,II型胶原蛋白的隐蔽肽序列诱导胶原酶活性的同时伴有软骨细胞肥大,并与细胞和基质变化相关。这种诱导发生在先前健康的关节软骨的中层和表层区域。软骨细胞对变性II型胶原蛋白隐蔽序列的这种反应可能在软骨内骨化的自然肥大以及骨关节炎软骨病理发展中起作用。

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