CNRS FRE 3235, Université Paris Descartes, Paris, France.
PLoS Pathog. 2013;9(5):e1003328. doi: 10.1371/journal.ppat.1003328. Epub 2013 May 2.
Productive HIV infection of CD4(+) T cells leads to a caspase-independent cell death pathway associated with lysosomal membrane permeabilization (LMP) and cathepsin release, resulting in mitochondrial outer membrane permeabilization (MOMP). Herein, we demonstrate that HIV infection induces damage-regulated autophagy modulator (DRAM) expression in a p53-dependent manner. Knocking down the expression of DRAM and p53 genes with specific siRNAs inhibited autophagy and LMP. However, inhibition of Atg5 and Beclin genes that prevents autophagy had a minor effect on LMP and cell death. The knock down of DRAM gene inhibited cytochrome C release, MOMP and cell death. However, knocking down DRAM, we increased viral infection and production. Our study shows for the first time the involvement of DRAM in host-pathogen interactions, which may represent a mechanism of defense via the elimination of infected cells.
HIV 对 CD4(+)T 细胞的有效感染会导致一种半胱天冬酶非依赖性细胞死亡途径,该途径与溶酶体膜通透性(LMP)和组织蛋白酶释放有关,最终导致线粒体外膜通透性(MOMP)。在此,我们证明 HIV 感染以依赖 p53 的方式诱导损伤调节自噬调节剂(DRAM)的表达。用特异性 siRNA 敲低 DRAM 和 p53 基因的表达会抑制自噬和 LMP。然而,抑制自噬的 Atg5 和 Beclin 基因的敲低对 LMP 和细胞死亡的影响较小。DRAM 基因的敲低抑制了细胞色素 C 的释放、MOMP 和细胞死亡。然而,敲低 DRAM 基因会增加病毒感染和产生。我们的研究首次表明,DRAM 参与了宿主-病原体的相互作用,这可能代表了通过消除受感染细胞来进行防御的一种机制。