Department of Biochemistry and Molecular Biology, Monash University, Clayton campus, Melbourne, Victoria 3000, Australia.
Cells. 2012 Jul 30;1(3):396-408. doi: 10.3390/cells1030396.
Autophagy is an intracellular degradative process with a number of roles, one of which can be the protection of eukaryotic cells from invading microbes. Microtubule-associated protein light-chain 3 (LC3) is a key autophagy-related protein that is recruited to the double-membrane autophagosome responsible for sequestering material intended for delivery to lysosomes. GFP-LC3 is widely used as a marker of autophagosome formation as denoted by the formation of green puncta when viewed by fluorescence microscopy. Recently, it has been demonstrated that LC3 can be recruited to other membranes including single-membrane phagosomes, in a process termed LC3-associated phagocytosis (LAP). Thus, the observation of green puncta in cells can no longer, by itself, be taken as evidence of autophagy. This review will clarify those features of LAP which serve to distinguish it from autophagy and that make connections with host autophagic responses in terms of infection by microbial pathogens. More specifically, it will refer to concurrent studies of the mechanism by which LAP is triggered in comparison to autophagy.
自噬是一种具有多种作用的细胞内降解过程,其中之一可以是保护真核细胞免受入侵微生物的侵害。微管相关蛋白轻链 3(LC3)是一种关键的自噬相关蛋白,它被招募到负责隔离递送至溶酶体的物质的双层自噬体上。GFP-LC3 被广泛用作自噬体形成的标记物,因为通过荧光显微镜观察可以看到绿色斑点的形成。最近,已经证明 LC3 可以被招募到其他膜上,包括单膜吞噬体,这个过程称为 LC3 相关吞噬作用(LAP)。因此,细胞中绿色斑点的观察本身不能再被视为自噬的证据。这篇综述将澄清 LAP 的那些特征,这些特征将其与自噬区分开来,并在微生物病原体感染方面与宿主自噬反应建立联系。更具体地说,它将参考同时进行的研究,以了解 LAP 与自噬相比被触发的机制。