Arakawa Satoko, Honda Shinya, Yamaguchi Hirofumi, Shimizu Shigeomi
Department of Pathological Cell Biology, Medical Research Institute, Tokyo Medical and Dental University.
Proc Jpn Acad Ser B Phys Biol Sci. 2017;93(6):378-385. doi: 10.2183/pjab.93.023.
ATG5 and ATG7 are considered to be essential molecules for the induction of autophagy. However, we found that cells lacking ATG5 or ATG7 can still form autophagosomes/autolysosomes and perform autophagic protein degradation when subjected to certain types of stress. Although the lipidation of LC3 is accepted as a good indicator of autophagy, this did not occur during ATG5/ATG7-independent alternative autophagy. Unlike conventional autophagy, autophagosomes appeared to be generated in a Rab9-dependent manner by the fusion of the phagophores with vesicles derived from the trans-Golgi and late endosomes. Therefore, mammalian autophagy can occur via at least two different pathways; the ATG5/ATG7-dependent conventional pathway and an ATG5/ATG7-independent alternative pathway.
ATG5和ATG7被认为是诱导自噬的关键分子。然而,我们发现缺乏ATG5或ATG7的细胞在受到某些类型的应激时,仍然可以形成自噬体/自溶酶体并进行自噬性蛋白质降解。尽管LC3的脂化被公认为是自噬的一个良好指标,但在不依赖ATG5/ATG7的替代性自噬过程中并未发生这种情况。与传统自噬不同,自噬体似乎是以Rab9依赖的方式由吞噬泡与源自反式高尔基体和晚期内体的囊泡融合产生的。因此,哺乳动物的自噬可以通过至少两种不同的途径发生;依赖ATG5/ATG7的传统途径和不依赖ATG5/ATG7的替代性途径。