Matsumoto Y, Shinzato T, Amano I, Takai I, Kimura Y, Morita H, Miwa M, Nakane K, Yoshikai Y, Maeda K
Department of Internal Medicine, Nagoya University Branch Hospital, Japan.
Biochem Biophys Res Commun. 1995 Oct 4;215(1):98-105. doi: 10.1006/bbrc.1995.2438.
Chronic renal failure (CRF) is often complicated by lymphopenia, which may be partly responsible for immune deficiency. We hypothesized that lymphopenia in CRF might result from apoptosis of T cells in vivo. To elucidate the involvement of Fas antigen which mediates apoptosis, we analyzed Fas expression on peripheral blood T cells in uremic non-dialyzed (non-HD) patients and hemodialysis (HD) patients. T cells from both uremic groups expressed Fas with higher intensity than control T cells. When two uremic groups were compared, Fas intensity on T cells was significantly higher in non-HD patients than in patients on HD. Moreover, uremic T cells were shown to undergo accelerated apoptosis when cultured in vitro, in correlation with Fas expression. Our results suggest that T cells in CRF may undergo apoptosis by the Fas system and that hemodialysis treatment has beneficial effects in the light of the inhibition of T cell apoptosis.
慢性肾衰竭(CRF)常伴有淋巴细胞减少,这可能是免疫缺陷的部分原因。我们推测CRF中的淋巴细胞减少可能是体内T细胞凋亡所致。为阐明介导凋亡的Fas抗原的作用,我们分析了未透析的尿毒症患者(非血液透析患者)和血液透析(HD)患者外周血T细胞上Fas的表达。两个尿毒症组的T细胞表达Fas的强度均高于对照T细胞。比较两个尿毒症组时,非血液透析患者T细胞上的Fas强度显著高于血液透析患者。此外,尿毒症T细胞在体外培养时显示出加速凋亡,这与Fas表达相关。我们的结果表明,CRF中的T细胞可能通过Fas系统发生凋亡,并且从抑制T细胞凋亡的角度来看,血液透析治疗具有有益作用。