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兔腹膜巨噬细胞释放软骨细胞刺激因子。

Release of chondrocyte-stimulating factor by rabbit peritoneal macrophages.

作者信息

Phadke K, Nanda S, Marder P, Carlson D G

出版信息

Clin Exp Immunol. 1981 Feb;43(2):408-16.

Abstract

Cultured rabbit peritoneal macrophages, after stimulation with lipopolysaccharides (LPS), produce a factor that induces normal rabbit articular cartilage cells (chondrocytes) to release collagenase and other neutral proteases in their culture medium. The release of the factor as well as the activation of chondrocytes can be significantly inhibited by paramethasone (10(-6) M). Rabbit peripheral blood monocytes produce this factor in smaller quantities. Activation with LPS does not enhance the release of factor any further by these cells. Lymphocytes have no direct effect on the chondrocytic protease synthesis. Furthermore, conditioned medium of activated lymphocytes failed to stimulate monocytes or macrophages in the absence of LPS. The macrophage medium exhibits mitogenic and phytohaemagglutinin-enhancing activity towards thymocytes of C3H/HeJ mice, but not against species-specific rabbit lymphocytes. The lymphocyte-activating factor, derived from a mouse macrophage cell line, P388D1 cells, or from other sources, was unable to stimulate chondrocytic protease secretion. Such specific induction of chondrocytic proteases by a macrophage-derived factor may have an important role in cartilage destruction in arthritic conditions, where synovium is only marginally involved.

摘要

用脂多糖(LPS)刺激培养的兔腹膜巨噬细胞后,会产生一种因子,该因子可诱导正常兔关节软骨细胞(软骨细胞)在其培养基中释放胶原酶和其他中性蛋白酶。对甲基强的松龙(10⁻⁶M)可显著抑制该因子的释放以及软骨细胞的活化。兔外周血单核细胞产生的这种因子数量较少。LPS激活这些细胞不会进一步增强因子的释放。淋巴细胞对软骨细胞蛋白酶合成没有直接影响。此外,在没有LPS的情况下,活化淋巴细胞的条件培养基无法刺激单核细胞或巨噬细胞。巨噬细胞培养基对C3H/HeJ小鼠的胸腺细胞具有促有丝分裂和增强植物血凝素的活性,但对种属特异性兔淋巴细胞则无此作用。源自小鼠巨噬细胞系P388D1细胞或其他来源的淋巴细胞激活因子无法刺激软骨细胞蛋白酶分泌。巨噬细胞衍生因子对软骨细胞蛋白酶的这种特异性诱导在关节炎病症的软骨破坏中可能起重要作用,在这些病症中滑膜仅轻微受累。

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