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再生与耐受因子调节三磷酸腺苷诱导人巨噬细胞分泌白细胞介素1β的作用。

Regeneration and tolerance factor modulates the effect of adenosine triphosphate-induced interleukin 1 beta secretion in human macrophages.

作者信息

Derks Richard, Beaman Kenneth

机构信息

Department of Microbiology and Immunology, Finch University of Health Sciences, The Chicago Medical School, North Chicago, IL 60064, USA.

出版信息

Hum Immunol. 2004 Jul;65(7):676-82. doi: 10.1016/j.humimm.2004.04.006.

Abstract

These studies characterize a molecule known as regeneration and tolerance factor (RTF), which controls inflammation by regulating interleukin 1 beta (IL-1 beta) secretion. Recently, it has been demonstrated that the interaction of adenosine triphosphate (ATP) with the P2X7 purinoceptor induces the secretion of IL-1 beta and initiates the inflammatory response. In these experiments, that the addition of ATP to macrophages was found to induce P2X7 activation and secretion of IL-1 beta. This secretion is enhanced with anti-RTF antibody in combination with exogenous ATP (p< 0.005). RTF is also revealed to be able to influence surface ATPase activity and, increase PI incorporation, which is an indicator of P2X7 activation. We demonstrate that RTF has a role in controlling IL-1 beta secretion by regulating P2X7 activity.

摘要

这些研究对一种名为再生与耐受因子(RTF)的分子进行了表征,该分子通过调节白细胞介素1β(IL-1β)的分泌来控制炎症。最近,有研究表明三磷酸腺苷(ATP)与P2X7嘌呤受体的相互作用会诱导IL-1β的分泌并引发炎症反应。在这些实验中,发现向巨噬细胞中添加ATP会诱导P2X7激活和IL-1β的分泌。抗RTF抗体与外源性ATP联合使用时,这种分泌会增强(p<0.005)。还发现RTF能够影响表面ATP酶活性,并增加磷脂酰肌醇(PI)掺入,这是P2X7激活的一个指标。我们证明RTF通过调节P2X7活性在控制IL-1β分泌中发挥作用。

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