Waring P, Lambert D, Sjaarda A, Hurne A, Beaver J
Division of Immunology and Cell Biology, John Curtin School of Medical Research, Australian National University, PO Box 334, Canberra, Australia.
Cell Death Differ. 1999 Jul;6(7):624-37. doi: 10.1038/sj.cdd.4400540.
Phosphatidylserine (PS) exposure on propidium iodide negative cells using FITC labelled annexin-V has been used to quantify apoptosis in vitro and in vivo. Detection of PS within cells undergoing necrosis is also possible if labelled annexin-V specific for PS enters the cell following early membrane damage. Necrotic or late apoptotic cells can be excluded from flow cytometric analysis using propidium iodide which enters and stains cells with compromised membrane integrity. Here we show that thymocytes undergoing death exclusively by necrosis show early exposure of PS prior to loss of membrane integrity. This early exposure of PS occurs in cells treated with agents which both raise intracellular calcium levels and are also capable of interacting with protein thiol groups. We also demonstrate that PS exposure in thymocytes induced to undergo apoptosis by three different agents does not correlate with calcium rises but correlates with and precedes DNA fragmentation.
使用异硫氰酸荧光素(FITC)标记的膜联蛋白V来检测碘化丙啶阴性细胞上的磷脂酰丝氨酸(PS)暴露,已被用于在体外和体内定量细胞凋亡。如果针对PS的标记膜联蛋白V在早期膜损伤后进入细胞,那么也可以检测正在经历坏死的细胞内的PS。使用碘化丙啶可以将坏死或晚期凋亡细胞排除在流式细胞术分析之外,碘化丙啶会进入并染色膜完整性受损的细胞。在这里,我们表明仅通过坏死死亡的胸腺细胞在膜完整性丧失之前就显示出PS的早期暴露。PS的这种早期暴露发生在用既能提高细胞内钙水平又能与蛋白质硫醇基团相互作用的试剂处理的细胞中。我们还证明,由三种不同试剂诱导发生凋亡的胸腺细胞中的PS暴露与钙升高无关,但与DNA片段化相关且先于DNA片段化。