Mori T, Ando K, Tanaka K, Ikeda Y, Koga Y
Department of Infectious Diseases, Tokai University School of Medicine, Kanagawa, Japan.
Blood. 1997 May 15;89(10):3565-73.
The effects of cytomegalovirus (CMV) infection on hematopoietic progenitor cells in vivo were investigated to elucidate the pathogenesis of CMV-induced myelosuppression. BALB/c mice were inoculated with 0.2LD50 of murine CMV (MCMV). Lineage marker negative, c-kit positive (Lin-c-kit+) and Lin-CD34+ cells, which are both phenotypically defined as hematopoietic progenitor cells, showed a significant reduction in number on day 3 postinfection (pi). Moreover, the reduction in the number of day-14 colony-forming units-spleen (CFU-S), another indicator to identify hematopoietic progenitor cells, was noted on day 3 pi. To clarify the mechanism of such depletion, we examined the cells undergoing apoptosis in the Lin- populations and found a 15-fold increase in the apoptosis-induction of these cells. Furthermore, an increase in the expression level of Fas, which mediates apoptosis, was observed in such Lin-c-kit+ and Lin-Sca-1+ cells on day 3 pi. In vitro treatment with the anti-Fas antibody accelerated the apoptosis in Lin- cells, but not in the uninfected control cells, thus indicating that the upregulated Fas on Lin- cells is directly related to the acceleration of apoptosis found in these cells in vivo. These results suggest that MCMV infection reduces the number of hematopoietic progenitor cells in bone marrow at least in part due to Fas-mediated apoptosis, and this phenomenon is thus considered to contribute to CMV-induced myelosuppression.
为阐明巨细胞病毒(CMV)诱导骨髓抑制的发病机制,研究了CMV感染对体内造血祖细胞的影响。给BALB/c小鼠接种0.2LD50的鼠巨细胞病毒(MCMV)。谱系标记阴性、c-kit阳性(Lin-c-kit+)和Lin-CD34+细胞,这两种细胞在表型上都被定义为造血祖细胞,在感染后第3天(pi)数量显著减少。此外,在感染后第3天,另一种识别造血祖细胞的指标——第14天脾集落形成单位(CFU-S)数量也减少。为阐明这种耗竭的机制,我们检查了Lin-群体中正在经历凋亡的细胞,发现这些细胞的凋亡诱导增加了15倍。此外,在感染后第3天,在这些Lin-c-kit+和Lin-Sca-1+细胞中观察到介导凋亡的Fas表达水平增加。用抗Fas抗体进行体外处理可加速Lin-细胞的凋亡,但未感染的对照细胞则无此现象,这表明Lin-细胞上上调的Fas与体内这些细胞中发现的凋亡加速直接相关。这些结果表明,MCMV感染至少部分由于Fas介导的凋亡而减少了骨髓中造血祖细胞的数量,因此这种现象被认为是CMV诱导骨髓抑制的原因之一。