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激活素A对白细胞介素-6生物活性的抑制作用及其对炎性关节病的影响。

Suppression of IL-6 biological activities by activin A and implications for inflammatory arthropathies.

作者信息

Yu E W, Dolter K E, Shao L E, Yu J

机构信息

Department of Molecular and Experimental Medicine, The Scripps Research Institute, La Jolla, CA 92037, USA.

出版信息

Clin Exp Immunol. 1998 Apr;112(1):126-32. doi: 10.1046/j.1365-2249.1998.00522.x.

Abstract

Activin A is a cytokine whose multiple functions have yet to be fully determined. In this study, the role of proinflammatory cytokines in regulatory control of activin A production was shown in synoviocytes and chondrocytes. Additional facets of functional inflammation-related activities of activin A were also determined. Results showed that activin A concentrations in the synovial fluid of patients with rheumatoid arthritis and gout were elevated relative to those in patients with osteoarthritis. Further studies showed that production of activin A by synoviocytes and chondrocytes in culture was stimulated by cytokines such as IL-1, transforming growth factor-beta (TGF-beta), interferon-gamma (IFN-gamma), and IL-8, consistent with previous studies in regard to the control of activin A production in marrow stromal cells and monocytes by cytokines, glucocorticoids and retinoic acid. In addition, the relationship of activin A to IL-6-induced biological activities was investigated. Three major IL-6 activities involved in inflammatory responses were found to be suppressed by activin A. In a dose-dependent manner, activin A efficiently suppressed IL-6-induced proliferation of 7TD1 B lymphoid cells, phagocytic activity of monocytic M1 cells, and fibrinogen production in HepG2. Therefore, it is likely that activin A serves as a suppressor for IL-6, dampening inflammatory responses, and has the potential to perform some previously unrecognized roles in inflammation.

摘要

激活素A是一种细胞因子,其多种功能尚未完全确定。在本研究中,促炎细胞因子在滑膜细胞和软骨细胞中对激活素A产生的调节控制作用得以展现。激活素A与炎症相关的功能活动的其他方面也得到了确定。结果显示,类风湿性关节炎和痛风患者滑液中的激活素A浓度相对于骨关节炎患者有所升高。进一步研究表明,培养中的滑膜细胞和软骨细胞产生激活素A受到白细胞介素-1(IL-1)、转化生长因子-β(TGF-β)、干扰素-γ(IFN-γ)和IL-8等细胞因子的刺激,这与之前关于细胞因子、糖皮质激素和视黄酸对骨髓基质细胞和单核细胞中激活素A产生的控制研究一致。此外,还研究了激活素A与IL-6诱导的生物学活性之间的关系。发现激活素A抑制了参与炎症反应的三种主要IL-6活性。激活素A以剂量依赖的方式有效抑制了IL-6诱导的7TD1 B淋巴细胞增殖、单核细胞M1细胞的吞噬活性以及HepG2细胞中纤维蛋白原的产生。因此,激活素A很可能作为IL-6的抑制剂,减轻炎症反应,并有可能在炎症中发挥一些先前未被认识的作用。

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