Kasai T, Ohguchi K, Nakashima S, Ito Y, Naganawa T, Kondo N, Nozawa Y
Department of Pediatrics, Gifu University School of Medicine, Japan.
J Immunol. 1998 Dec 15;161(12):6469-74.
Apoptosis is an active form of cell death that can be induced by a wide variety of agents and conditions. In response to actinomycin D, hydrogen peroxide (H2O2), or TNF-alpha, Jurkat T cells underwent typical apoptosis. Phospholipase D (PLD) activity in intact cells determined by phosphatidylbutanol generation was up-regulated by these agents. The PLD activation was in a time-dependent manner during apoptosis. It was also shown that the PLD activity measured by using exogenous substrate in the lysate from apoptotic cells was higher than that in the lysate from control untreated cells. The PLD activity in lysate from control untreated cells was stimulated by unsaturated fatty acids (UFA), but not by guanosine 5'-O-(3-thiotriphosphate). However, the PLD activity in the apoptotic cell lysate was no longer enhanced by the addition of oleate, suggesting that the increased PLD activity during apoptosis was attributed to the PLD of UFA-dependent type, but not the small G protein-dependent one. In fact, the release of free UFA was increased during apoptosis. The caspase inhibitors, z-DEVD and z-VAD, effectively suppressed PLD activation and apoptosis, but UFA release was unaffected. These results suggest the possibility that UFA-dependent type PLD may be implicated in apoptotic process in Jurkat T cells. This is the first demonstration that the PLD of UFA-dependent type would be involved in cellular responses.
细胞凋亡是一种细胞死亡的主动形式,可由多种因素和条件诱导。在放线菌素D、过氧化氢(H2O2)或肿瘤坏死因子-α的作用下,Jurkat T细胞发生典型的细胞凋亡。通过磷脂酰丁醇生成测定的完整细胞中的磷脂酶D(PLD)活性被这些因素上调。在细胞凋亡过程中,PLD的激活呈时间依赖性。还表明,用凋亡细胞裂解物中的外源性底物测量的PLD活性高于未处理对照细胞裂解物中的活性。未处理对照细胞裂解物中的PLD活性受到不饱和脂肪酸(UFA)的刺激,但不受鸟苷5'-O-(3-硫代三磷酸)的刺激。然而,凋亡细胞裂解物中的PLD活性不再因添加油酸而增强,这表明细胞凋亡过程中PLD活性的增加归因于UFA依赖性类型的PLD,而不是小G蛋白依赖性的PLD。事实上,在细胞凋亡过程中游离UFA的释放增加。半胱天冬酶抑制剂z-DEVD和z-VAD有效抑制PLD激活和细胞凋亡,但UFA释放不受影响。这些结果表明,UFA依赖性类型的PLD可能参与Jurkat T细胞的凋亡过程。这是首次证明UFA依赖性类型的PLD参与细胞反应。