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软骨细胞介导的软骨降解:前列腺素E2、环磷酸腺苷和α干扰素的调节作用

Chondrocyte mediated cartilage degradation: regulation by prostaglandin E2, cyclic AMP and interferon alpha.

作者信息

Steinberg J J, Sledge C B

机构信息

Department of Medicine, Brigham and Women's Hospital, Harvard Medical School, Boston, MA 02115.

出版信息

J Rheumatol Suppl. 1991 Feb;27:63-5.

PMID:1851230
Abstract

Local responses to cytokines and their induced products play a critical role in outcome in the arthritic joint. Using a bovine nasal cartilage culture model, chondrocyte mediated breakdown was stimulated by lipopolysaccharides or tumor necrosis factor. Cartilage breakdown was inhibited in a dose dependent manner by prostaglandin E2, cyclic AMP enhancement and interferon alpha. The possible regulatory roles played by these agents in cytokine activated cartilage breakdown suggest potential therapeutic strategies in human arthritis.

摘要

对细胞因子及其诱导产物的局部反应在关节炎关节的转归中起关键作用。利用牛鼻软骨培养模型,脂多糖或肿瘤坏死因子可刺激软骨细胞介导的破坏。前列腺素E2、环磷酸腺苷增强剂和α干扰素可剂量依赖性地抑制软骨破坏。这些因子在细胞因子激活的软骨破坏中可能发挥的调节作用提示了人类关节炎的潜在治疗策略。

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