Souvannavong V, Lemaire C, Brown S, Adam A
Centre national de la recherche scientifique, Unité de recherche associée 1116, Institut de biochimie, Université Paris-Sud, Orsay, France.
Biochem Cell Biol. 1997;75(6):783-8.
Expression of alkaline phosphatase (APase) by 7TD1 B-cell hybridoma was amplified by ultraviolet irradiation; cell growth was inhibited and cell death by apoptosis was increased. Irradiation induced high levels of APase activity in cycling as well as in apoptotic cells. In contrast, APase activity faded with time in nonirradiated cells and was no longer expressed in spontaneous apoptotic cells appearing after several days in culture. This was demonstrated by cell morphology, DNA fragmentation, and flow cytometry after simultaneous staining of DNA with Hoechst 33342 and APase with naphthol AS-TR phosphate--fast red RC fluorescent reagent. Levamisole, a specific inhibitor of APase activity, almost totally abrogated apoptosis induced by ultraviolet irradiation at doses that failed to affect 7TD1 cell survival. These data suggest that APase could play a role in the signalling cascade that mediates apoptosis in irradiated cells.
紫外线照射可增强7TD1 B细胞杂交瘤碱性磷酸酶(APase)的表达;细胞生长受到抑制,凋亡导致的细胞死亡增加。照射在增殖细胞和凋亡细胞中均诱导出高水平的APase活性。相反,未照射细胞中的APase活性随时间逐渐消失,且在培养几天后出现的自发凋亡细胞中不再表达。在用Hoechst 33342对DNA进行同步染色并用萘酚AS-TR磷酸酯-固红RC荧光试剂对APase进行染色后,通过细胞形态学、DNA片段化和流式细胞术证实了这一点。左旋咪唑是APase活性的特异性抑制剂,在不影响7TD1细胞存活的剂量下,几乎完全消除了紫外线照射诱导的凋亡。这些数据表明,APase可能在介导照射细胞凋亡的信号级联反应中发挥作用。