Derks Richard, Beaman Kenneth
Department of Microbiology and Immunology, Finch University of Health Sciences, The Chicago Medical School, North Chicago, IL 60064, USA.
Hum Immunol. 2004 Jul;65(7):676-82. doi: 10.1016/j.humimm.2004.04.006.
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.
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。