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TPC2 介导癌细胞中的自噬进展和细胞外囊泡分泌。

TPC2 mediates autophagy progression and extracellular vesicle secretion in cancer cells.

机构信息

City University of Hong Kong ShenZhen Research Institute, ShenZhen, China; Department of Biomedical Sciences, City University of Hong Kong, Hong Kong, China.

City University of Hong Kong ShenZhen Research Institute, ShenZhen, China; Department of Biomedical Sciences, City University of Hong Kong, Hong Kong, China.

出版信息

Exp Cell Res. 2018 Sep 15;370(2):478-489. doi: 10.1016/j.yexcr.2018.07.013. Epub 2018 Jul 7.

Abstract

Autophagy is an evolutionarily conserved lysosomal degradation process, and is involved in various cellular processes. Here we studied the role of two pore channel 2 (TPC2), a lysosomal non-selective Na/Ca channel, in autophagy progression. We found that TPC overexpression in 4T1 mouse breast cancer cell line or in HeLa human cervical cancer cell line inhibited the fusion between autophagosome and lysosome, resulting in the accumulation of autophagosomes accompanied with increased lysosomal pH and TFEB nuclear localization. Interestingly, we also found that extracellular vesicle (EV) secretion was markedly decreased in TPC2 overexpressing cells but was induced in TPC2 knockdown cells. In addition, migration of TPC2 knockdown cells, not TPC2 overexpressing cells, was inhibited. Taken together, these results support a role of TPC2 in autophagy progression and EV trafficking in cancer cells.

摘要

自噬是一种进化上保守的溶酶体降解过程,参与各种细胞过程。在这里,我们研究了两个孔道蛋白 2(TPC2),一种溶酶体非选择性的 Na/Ca 通道,在自噬进展中的作用。我们发现,在 4T1 小鼠乳腺癌细胞系或 HeLa 人宫颈癌细胞系中过表达 TPC2 会抑制自噬体与溶酶体之间的融合,导致自噬体积累,同时溶酶体 pH 值升高和 TFEB 核定位增加。有趣的是,我们还发现 TPC2 过表达细胞中细胞外囊泡(EV)的分泌明显减少,而 TPC2 敲低细胞中 EV 的分泌则增加。此外,TPC2 敲低细胞的迁移受到抑制,而 TPC2 过表达细胞的迁移不受影响。总之,这些结果支持 TPC2 在癌细胞自噬进展和 EV 运输中的作用。

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