Cecconi Francesco, Levine Beth
Dulbecco Telethon Institute at the Department of Biology, University of Rome Tor Vergata, 00133 Rome, Italy; Laboratory of Molecular Neuroembryology, IRCCS Fondazione Santa Lucia, 00143 Rome, Italy.
Howard Hughes Medical Institute, Southwestern Medical Center, University of Texas, Dallas, TX 75390, USA; Department of Internal Medicine, Southwestern Medical Center, University of Texas, Dallas, TX 75390, USA; Department of Microbiology, Southwestern Medical Center, University of Texas, Dallas, TX 75390, USA.
Dev Cell. 2008 Sep;15(3):344-357. doi: 10.1016/j.devcel.2008.08.012.
Autophagy is important for the degradation of bulk cytoplasm, long-lived proteins, and entire organelles. In lower eukaryotes, autophagy functions as a cell death mechanism or as a stress response during development. However, autophagy's significance in vertebrate development, and the role (if any) of vertebrate-specific factors in its regulation, remains unexplained. Through careful analysis of the current autophagy gene mutant mouse models, we propose that in mammals, autophagy may be involved in specific cytosolic rearrangements needed for proliferation, death, and differentiation during embryogenesis and postnatal development. Thus, autophagy is a process of cytosolic "renovation," crucial in cell fate decisions.
自噬对于大量细胞质、长寿命蛋白质及整个细胞器的降解至关重要。在低等真核生物中,自噬在发育过程中作为一种细胞死亡机制或应激反应发挥作用。然而,自噬在脊椎动物发育中的意义以及脊椎动物特异性因子在其调控中的作用(如果有的话)仍未得到解释。通过对当前自噬基因敲除小鼠模型的仔细分析,我们提出,在哺乳动物中,自噬可能参与胚胎发生和出生后发育过程中增殖、死亡及分化所需的特定胞质重排。因此,自噬是一种胞质“更新”过程,在细胞命运决定中至关重要。