Nagafuji K, Takenaka K, Niho Y
Dep. of Hematology, Hara Sanshin General Hospital.
Nihon Rinsho. 1996 Jul;54(7):1790-6.
We investigated the expression of Fas(CD95) on hematopoietic progenitor cells. CD34+ cells freshly isolated from bone marrow did not express Fas. However, interferon-gamma(IFN-gamma) and/or tumor necrosis factor-alpha (TNF-alpha) induced the expression of Fas after 48 hours of serum-free culture. The TNF-alpha-induced Fas expression is mediated by p55-TNF-alpha receptor. Human CD34+ cells expressed Fas following low dose ionizing radiation in a dose-dependent fashion. CD34+ cells isolated from bone marrow were cultured with hematopoietic growth factors for 7 days. CD34+ cells cultured with hematopoietic growth factors gradually became positive for Fas and rapidly lost Bcl-2 expression. Fas system is considered to play important roles at the level of hematopoietic progenitor cells in both physiologic and pathologic conditions.
我们研究了造血祖细胞上Fas(CD95)的表达。从骨髓中新鲜分离的CD34+细胞不表达Fas。然而,在无血清培养48小时后,γ干扰素(IFN-γ)和/或肿瘤坏死因子-α(TNF-α)诱导了Fas的表达。TNF-α诱导的Fas表达由p55-TNF-α受体介导。人CD34+细胞在低剂量电离辐射后以剂量依赖方式表达Fas。从骨髓中分离的CD34+细胞与造血生长因子一起培养7天。与造血生长因子一起培养的CD34+细胞逐渐Fas呈阳性,并迅速丧失Bcl-2表达。Fas系统被认为在生理和病理条件下的造血祖细胞水平上发挥重要作用。