Zhang Yi, Foster Robert, Sun Xiuli, Yin Qiaoqiao, Li Yi, Hanley Gregory, Stuart Charles, Gan Yili, Li Chuanfu, Zhang Zhiyong, Yin Deling
Department of Internal Medicine, College of Medicine, East Tennessee State University, Johnson City, TN 37614, United States.
J Neuroimmunol. 2008 Aug 30;200(1-2):71-6. doi: 10.1016/j.jneuroim.2008.06.014. Epub 2008 Jul 24.
Restraint stress, either physical or psychological, can modulate immune function. However, the mechanisms associated with stress-induced lymphocyte reduction remains to be elucidated. We have previously shown that chronic stress induces Fas-mediated lymphocyte reduction. Here, we investigated the mechanisms by which restraint stress modulates lymphocyte reduction. Our data have shown that inhibition of p53 by the p53 inhibitor PFT-alpha attenuates stress-induced reduction in lymphocyte numbers. These results were verified using p53 knockout mice, suggesting a pivotal role of p53 in this process. In addition our data have indicated that PI3K/nuclear factor kappa B (NF-kappaB) signaling pathway plays an important role in the stress-induced lymphocyte reduction. Our study thus demonstrates that restraint stress promotes lymphocyte reduction through p53 and PI3K/NF-kappaB pathways.
身体或心理上的束缚应激都可以调节免疫功能。然而,与应激诱导的淋巴细胞减少相关的机制仍有待阐明。我们之前已经表明,慢性应激会诱导Fas介导的淋巴细胞减少。在此,我们研究了束缚应激调节淋巴细胞减少的机制。我们的数据表明,p53抑制剂PFT-α对p53的抑制作用减弱了应激诱导的淋巴细胞数量减少。使用p53基因敲除小鼠验证了这些结果,表明p53在此过程中起关键作用。此外,我们的数据表明,PI3K/核因子κB(NF-κB)信号通路在应激诱导的淋巴细胞减少中起重要作用。因此,我们的研究表明,束缚应激通过p53和PI3K/NF-κB途径促进淋巴细胞减少。