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培养的关节软骨细胞及骨关节炎软骨中β1整合素的表达

Expression of beta 1 integrins by cultured articular chondrocytes and in osteoarthritic cartilage.

作者信息

Loeser R F, Carlson C S, McGee M P

机构信息

Department of Internal Medicine, Bowman Gray School of Medicine of Wake Forest University, Winston-Salem, North Carolina 27157, USA.

出版信息

Exp Cell Res. 1995 Apr;217(2):248-57. doi: 10.1006/excr.1995.1084.

Abstract

Expression of beta 1 integrins was studied in vitro as articular chondrocytes reestablished a matrix in culture and in situ in a nonhuman primate model of osteoarthritis in order to investigate a potential role for integrins in mediating cell-extracellular matrix interactions in cartilage. Chondrocytes were found to express alpha 1 beta 1, alpha 3 beta 1, and alpha 5 beta 1 integrins both in vitro and in situ. Cell surface expression of beta 1 integrins increased as chondrocytes were maintained in cultured from 3 to 7 days. Increased beta 1 integrin expression was also observed in osteoarthritic cartilage compared with normal cartilage. The greatest relative increase in both systems was noted for the alpha 1 beta 1 integrin. The increase in chondrocyte beta 1 integrin expression in vitro was noted in both monolayer and alginate cultures and occurred prior to detectable changes in the differentiated phenotype of the chondrocyte. Disruption of the cytoskeleton with the drug dihydrocytochalasin B inhibited the cell culture induced increase in integrin expression, while treatment of cultured cells with TGF-beta resulted in increased expression of the alpha 5 beta 1 integrin. The modulation of beta 1 integrin expression noted in vitro and in situ indicates that chondrocytes are capable of regulated expression of beta 1 integrins and suggests that beta 1 integrins may play an important role in mediating chondrocyte-extracellular matrix interactions in cartilage.

摘要

为了研究整合素在介导软骨细胞与细胞外基质相互作用中的潜在作用,我们在体外研究了β1整合素的表达,此时关节软骨细胞在培养物中重新建立基质,并在非人类灵长类骨关节炎模型中进行原位研究。发现软骨细胞在体外和原位均表达α1β1、α3β1和α5β1整合素。随着软骨细胞在培养中维持3至7天,β1整合素的细胞表面表达增加。与正常软骨相比,骨关节炎软骨中也观察到β1整合素表达增加。在两个系统中,α1β1整合素的相对增加最为显著。在单层和藻酸盐培养中均注意到软骨细胞β1整合素表达在体外增加,且发生在软骨细胞分化表型出现可检测变化之前。用药物二氢细胞松弛素B破坏细胞骨架可抑制细胞培养诱导的整合素表达增加,而用转化生长因子-β处理培养细胞则导致α5β1整合素表达增加。在体外和原位观察到的β1整合素表达调节表明,软骨细胞能够调节β1整合素的表达,并提示β1整合素可能在介导软骨细胞与细胞外基质相互作用中发挥重要作用。

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