首页> 外文期刊>Biochimica et biophysica acta. Molecular cell research >Integrin alpha 1 beta 1 mediates collagen induction of MMP-13 expression in MC615 chondrocytes
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Integrin alpha 1 beta 1 mediates collagen induction of MMP-13 expression in MC615 chondrocytes

机译:整合素α1beta 1介导MC615软骨细胞中MMP-13表达的胶原蛋白诱导。

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摘要

During endochondral ossification, type I collagen is synthesized by osteoblasts together with some hypertrophic chondrocytes. Type I collagen has also been reported to be progressively synthesized in degenerative joints. Because Matrix Metalloproteinase-13 (MMP-13) plays an active role in remodeling cartilage in fetal development and osteoarthritic cartilage, we investigated whether type I collagen could activate MMP-13 expression in chondrocytes. We used a well-established chondrocytic cell line (MC615) and we found that MMP-13 expression was induced in MC615 cells cultured in type I collagen gel. We also found that a I I integrin, a major collagen receptor, was expressed by MC615 cells and we further assessed the role of alpha 1 beta 1 integrin in conducting MMP-13 expression. Induction of MMP-13 expression by collagen was potently and synergistically inhibited by blocking antibodies against alpha 1 and beta 1 integrin subunits, indicating that alpha 1 beta 1 integrin mediates the MMP-13-inducing cellular signal generated by three-dimensional type I collagen. We also determined that activities of tyrosine kinase and ERK and JNK MAP kinases were required for this collagen-induced MMP-13 expression. Interestingly, bone morphogenetic protein (BMP)-2 opposed this induction, an effect that may be related to a role of BMP-2 in the maintenance of cartilage matrix. (c) 2005 Elsevier B.V All rights reserved.
机译:在软骨内骨化过程中,I型胶原由成骨细胞与一些肥大的软骨细胞合成。据报道,I型胶原在退化性关节中逐渐合成。由于基质金属蛋白酶-13(MMP-13)在胎儿发育和骨关节炎软骨重塑中起着积极作用,因此我们研究了I型胶原是否可以激活软骨细胞中MMP-13的表达。我们使用了成熟的软骨细胞系(MC615),我们发现在I型胶原凝胶中培养的MC615细胞中诱导了MMP-13表达。我们还发现MC615细胞表达了一种主要的胶原受体I I整合素,我们进一步评估了α1 beta 1整合素在进行MMP-13表达中的作用。阻断α1和β1整联蛋白亚基抗体可有效和协同抑制胶原蛋白对MMP-13表达的诱导,表明α1β1整联蛋白介导了三维I型胶原蛋白产生的MMP-13诱导细胞信号。我们还确定,这种胶原蛋白诱导的MMP-13表达需要酪氨酸激酶,ERK和JNK MAP激酶的活性。有趣的是,骨形态发生蛋白(BMP)-2反对这种诱导作用,这种作用可能与BMP-2在维持软骨基质中的作用有关。 (c)2005 Elsevier B.V保留所有权利。

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