Department of Biological Sciences Centre for BioImaging Sciences, National University of Singapore, 117543 Singapore.
Cell Microbiol. 2012 Aug;14(8):1242-56. doi: 10.1111/j.1462-5822.2012.01795.x. Epub 2012 Apr 24.
The early branching eukaryote Trypanosoma brucei contains functional autophagy machinery that allows regulated degradation of its own cellular components. In this study, we examined the function of two Atg8 genes, TbAtg8.1 and TbAtg8.2, in starvation-induced autophagosome formation and cell death in procyclic T. brucei. Upon starvation, both TbAtg8.1 and TbAtg8.2 localize to punctate structures characteristic of autophagosomes as shown by fluorescence and electron microscopy, and wortmannin and chloroquine treatments. While TbAtg8.1 depletion has no detectable effects on TbAtg8.2 recruitment to autophagosomes, TbAtg8.2 depletion greatly reduced the autophagosome relocation of TbAtg8.1. Depletion of TbAtg8.1 and 8.2, individually or together, promote cell survival under starvation conditions. Taken together, these observations confirm the presence of an autophagy-related cell death pathway in T. brucei, where TbAtg8.1 and TbAtg8.2 play essential but distinct roles in autophagosome formation and cell death.
早期分支真核生物布氏锥虫含有功能正常的自噬机制,允许自身细胞成分的降解。在这项研究中,我们研究了两个 Atg8 基因(TbAtg8.1 和 TbAtg8.2)在饥饿诱导的前鞭毛体自噬体形成和细胞死亡中的作用。在饥饿状态下,如荧光和电子显微镜以及渥曼青霉素和氯喹处理所示,TbAtg8.1 和 TbAtg8.2 均定位于自噬体的点状结构。虽然 TbAtg8.1 的耗竭对 TbAtg8.2 招募到自噬体没有可检测到的影响,但 TbAtg8.2 的耗竭大大减少了 TbAtg8.1 的自噬体重定位。TbAtg8.1 和 8.2 的单独或联合耗竭均可促进在饥饿条件下细胞的存活。总之,这些观察结果证实了布氏锥虫中存在与自噬相关的细胞死亡途径,其中 TbAtg8.1 和 TbAtg8.2 在自噬体形成和细胞死亡中发挥着重要但不同的作用。