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视黄醇和地塞米松对培养的人关节软骨细胞和滑膜细胞中细胞因子介导的金属蛋白酶及其抑制剂调控的影响。

Effects of retinol and dexamethasone on cytokine-mediated control of metalloproteinases and their inhibitors by human articular chondrocytes and synovial cells in culture.

作者信息

McGuire-Goldring M K, Murphy G, Gowen M, Meats J E, Ebsworth N M, Poll C, Reynolds J J, Russell R G

出版信息

Biochim Biophys Acta. 1983 Sep 22;763(2):129-39. doi: 10.1016/0167-4889(83)90036-8.

Abstract

Human articular chondrocytes in culture produced large amounts of specific mammalian collagenase, gelatinase and proteoglycanase when exposed to dialysed supernatant medium derived from cultured human blood mononuclear cells (mononuclear cell factor) or to conditioned medium, partially purified by fractionation with ammonium sulphate (60-90% fraction), from cultures of human synovial tissue (synovial factor). Human chondrocytes and synovial cells also released into culture medium an inhibitor of collagenase of apparent molecular weight about 30 000, which appeared to be similar to the tissue inhibitor of metalloproteinases synthesised by tissues in culture. The amounts of free collagenase inhibitor were reduced in culture media from chondrocytes or synovial cells exposed to mononuclear cell factor or synovial factor. While retinol inhibited the production of collagenase brought about by mononuclear cell factor or synovial factor, it restored the levels of inhibitor, which were reduced in the presence of mononuclear cell factor or synovial factor. Dexamethasone markedly reduced the production of collagenase by synovial cells, while only partially inhibiting factor-stimulated collagenase production by chondrocytes. Addition of puromycin as an inhibitor of protein synthesis reduced the amounts of both collagenase and inhibitor to control or undetectable levels.

摘要

培养的人关节软骨细胞在暴露于源自培养的人血单核细胞的透析上清液培养基(单核细胞因子)或经硫酸铵分级分离(60 - 90%级分)部分纯化的人滑膜组织培养物的条件培养基(滑膜因子)时,会产生大量特定的哺乳动物胶原酶、明胶酶和蛋白聚糖酶。人软骨细胞和滑膜细胞还向培养基中释放一种表观分子量约为30000的胶原酶抑制剂,它似乎与培养组织合成的金属蛋白酶组织抑制剂相似。在暴露于单核细胞因子或滑膜因子的软骨细胞或滑膜细胞的培养基中,游离胶原酶抑制剂的量减少。虽然视黄醇抑制单核细胞因子或滑膜因子引起的胶原酶产生,但它恢复了在单核细胞因子或滑膜因子存在下减少的抑制剂水平。地塞米松显著降低滑膜细胞胶原酶的产生,而仅部分抑制因子刺激的软骨细胞胶原酶产生。添加嘌呤霉素作为蛋白质合成抑制剂可将胶原酶和抑制剂的量降低至对照水平或检测不到的水平。

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