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肿瘤坏死因子α通过一种独立于核因子κB受体活化因子配体(RANKL)且与之强烈协同的直接作用,有力地激活破骨细胞。

TNFalpha potently activates osteoclasts, through a direct action independent of and strongly synergistic with RANKL.

作者信息

Fuller Karen, Murphy Chiho, Kirstein Barrie, Fox Simon W, Chambers Timothy J

机构信息

Department of Cellular Pathology, St. George's Hospital Medical School, London SW17 ORE, United Kingdom.

出版信息

Endocrinology. 2002 Mar;143(3):1108-18. doi: 10.1210/endo.143.3.8701.

Abstract

TNFalpha is pivotal to the pathogenesis of inflammatory and possibly postmenopausal osteolysis. Much recent work has clarified mechanisms by which TNFalpha promotes osteoclastogenesis, but the means by which it activates osteoclasts to resorb bone remain uncertain. We found that very low concentrations of TNFalpha promoted actin ring formation, which correlates with functional activation in osteoclasts, both in osteoclasts formed in vitro and extracted from newborn rats. TNFalpha was equipotent with RANKL for this action. Activation by TNFalpha was unaffected by blockade of RANKL by OPG, its soluble decoy receptor, suggesting that this was due to a direct action on osteoclasts. Bone resorption was similarly directly and potently stimulated, in a RANKL-independent manner in osteoclasts, whether these were formed in vitro or in vivo. Interestingly, TNFalpha promoted actin ring formation at concentrations an order of magnitude below those required for osteoclastic differentiation. Moreover, TNFalpha strongly synergized with RANKL, such that miniscule concentrations of TNFalpha were sufficient to substantially augment osteoclast activation. The extreme sensitivity of osteoclasts to activation by TNFalpha suggests that the most sensitive osteolytic response of bone to TNFalpha is through activation of existing osteoclasts; and the strong synergy with RANKL provides a mechanism whereby increased osteolysis can be achieved without disturbance to the underlying pattern of osteoclastic localization.

摘要

肿瘤坏死因子α(TNFα)在炎症性及可能的绝经后骨质溶解的发病机制中起关键作用。近期的许多研究阐明了TNFα促进破骨细胞生成的机制,但它激活破骨细胞进行骨吸收的方式仍不明确。我们发现,极低浓度的TNFα就能促进肌动蛋白环的形成,这与破骨细胞的功能激活相关,无论是在体外形成的还是从新生大鼠中提取的破骨细胞中均如此。TNFα在这一作用上与核因子κB受体活化因子配体(RANKL)等效。TNFα的激活不受其可溶性诱饵受体骨保护素(OPG)对RANKL的阻断影响,这表明这是对破骨细胞的直接作用。无论是体外还是体内形成的破骨细胞,骨吸收同样以RANKL非依赖的方式受到直接且强效的刺激。有趣的是,TNFα促进肌动蛋白环形成的浓度比破骨细胞分化所需浓度低一个数量级。此外,TNFα与RANKL强烈协同,以至于极微量的TNFα就足以显著增强破骨细胞的激活。破骨细胞对TNFα激活的极端敏感性表明,骨对TNFα最敏感的溶骨反应是通过激活现有的破骨细胞实现的;并且与RANKL的强烈协同作用提供了一种机制,借此可以在不干扰破骨细胞定位的基本模式的情况下实现骨溶解增加。

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