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肿瘤坏死因子-α诱导U937细胞凋亡过程中的胞质酸化和溶酶体碱化

Cytosolic acidification and lysosomal alkalinization during TNF-alpha induced apoptosis in U937 cells.

作者信息

Nilsson Cathrine, Johansson Uno, Johansson Ann-Charlotte, Kågedal Katarina, Ollinger Karin

机构信息

Division of Experimental Pathology, Faculty of Health Sciences, Linköping University, S-581 85 Linköping, Sweden.

出版信息

Apoptosis. 2006 Jul;11(7):1149-59. doi: 10.1007/s10495-006-7108-5.

Abstract

Apoptosis is often associated with acidification of the cytosol and since loss of lysosomal proton gradient and release of lysosomal content are early events during apoptosis, we investigated if the lysosomal compartment could contribute to cytosolic acidification. After exposure of U937 cells to tumor necrosis factor-alpha, three populations; healthy, pre-apoptotic, and apoptotic cells, were identified by flow cytometry. These populations were investigated regarding intra-cellular pH and apoptosis-associated events. There was a drop in cytosolic pH from 7.2 +/- 0.1 in healthy cells to 6.8 +/- 0.1 in pre-apoptotic, caspase-negative cells. In apoptotic, caspase-positive cells, the pH was further decreased to 5.7 +/- 0.04. The cytosolic acidification was not affected by addition of specific inhibitors towards caspases or the mitochondrial F(0)F(1)-ATPase. In parallel to the cytosolic acidification, a rise in lysosomal pH from 4.3 +/- 0.3, in the healthy population, to 4.8 +/- 0.3 and 5.5 +/- 0.3 in the pre-apoptotic- and apoptotic populations, respectively, was detected. In addition, lysosomal membrane permeability increased as detected as release of cathepsin D from lysosomes to the cytosol in pre-apoptotic and apoptotic cells. We, thus, suggest that lysosomal proton release is the cause of the cytosolic acidification of U937 cells exposed to TNF-alpha.

摘要

细胞凋亡常与胞质溶胶酸化相关,由于溶酶体质子梯度丧失和溶酶体内容物释放是细胞凋亡过程中的早期事件,我们研究了溶酶体区室是否会导致胞质溶胶酸化。将U937细胞暴露于肿瘤坏死因子-α后,通过流式细胞术鉴定出三个群体:健康细胞、凋亡前期细胞和凋亡细胞。对这些群体的细胞内pH值和凋亡相关事件进行了研究。健康细胞的胞质pH值从7.2±0.1降至凋亡前期、半胱天冬酶阴性细胞的6.8±0.1。在凋亡的、半胱天冬酶阳性细胞中,pH值进一步降至5.7±0.04。添加针对半胱天冬酶或线粒体F(0)F(1)-ATP酶的特异性抑制剂不会影响胞质溶胶酸化。与胞质溶胶酸化同时,检测到溶酶体pH值从健康群体中的4.3±0.3分别升至凋亡前期群体和凋亡群体中的4.8±0.3和5.5±0.3。此外,在凋亡前期和凋亡细胞中,溶酶体膜通透性增加,表现为组织蛋白酶D从溶酶体释放到胞质溶胶中。因此,我们认为溶酶体质子释放是暴露于TNF-α的U937细胞胞质溶胶酸化的原因。

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