Meisenholder G W, Martin S J, Green D R, Nordberg J, Babior B M, Gottlieb R A
Scripps Research Institute, La Jolla, California 92037, USA.
J Biol Chem. 1996 Jul 5;271(27):16260-2. doi: 10.1074/jbc.271.27.16260.
Cytoplasmic acidification is now recognized as a feature of apoptosis in a variety of systems. However, its relation to other events in the process of apoptosis is not yet characterized. In this work, we examined the effect of BCL-2 overexpression on acidification mediated by cycloheximide treatment or Fas ligation in Jurkat T-lymphoblasts. We find that BCL-2 overexpression attenuates cytoplasmic acidification and apoptosis detected by annexin V labeling. Acidification and phosphatidylserine externalization were found to occur concurrently. We also examined the requirement for protease activation for cytoplasmic acidification to occur and found that inhibition of interleukin-1beta converting enzyme/CED-3 family proteases (using carbobenzoxy-Val-Ala-Asp-fluoromethylketone, an inhibitor of these proteases) prevents acidification and apoptosis mediated by Fas ligation. These studies suggest that BCL-2 acts at a point upstream of acidification and that protease activation is also upstream of acidification.
细胞质酸化现已被公认为多种系统中细胞凋亡的一个特征。然而,它与细胞凋亡过程中其他事件的关系尚未明确。在这项研究中,我们检测了BCL-2过表达对放线菌酮处理或Fas配体诱导的Jurkat T淋巴细胞母细胞酸化的影响。我们发现,BCL-2过表达可减弱膜联蛋白V标记检测到的细胞质酸化和细胞凋亡。酸化和磷脂酰丝氨酸外化同时发生。我们还检测了细胞质酸化发生时对蛋白酶激活的需求,发现抑制白细胞介素-1β转换酶/CED-3家族蛋白酶(使用苄氧羰基-Val-Ala-Asp-氟甲基酮,这些蛋白酶的一种抑制剂)可阻止Fas配体诱导的酸化和细胞凋亡。这些研究表明,BCL-2作用于酸化上游的某个位点,并且蛋白酶激活也在酸化上游。