Phagocytosis and macroautophagy/autophagy are 2 processes involved in lysosome-mediated clearance of extracellular and intracellular components, respectively. Recent studies have identified the recruitment of the autophagic protein LC3 during phagocytosis of apoptotic corpses in what is now called LC3-associated phagocytosis (LAP). LAP is a distinct process from autophagy but it relies on some members of the autophagy pathway to allow efficient degradation of the phagocytosed cargo.
View Article and Find Full Text PDFAutophagy is a cellular process that allows degradation by the lysosome of cytoplasmic components such as proteins or organelles. Many studies that used model organisms, showed that autophagy plays an important role in multiple developmental processes like degradation of mitochondria of spermatozoids after fertilization, fetal growth or resistance to nutrient starvation. It is also essential to programmed cell death.
View Article and Find Full Text PDFFor a long time, autophagy has been mainly studied in yeast or mammalian cell lines, and assays for analyzing autophagy in these models have been well described. More recently, the involvement of autophagy in various physiological functions has been investigated in multicellular organisms. Modification of autophagy flux is involved in developmental processes, resistance to stress conditions, aging, cell death and multiple pathologies.
View Article and Find Full Text PDFWe recently described in C. elegans embryos, the acquisition of specialized functions for orthologs of yeast Atg8 (e.g.
View Article and Find Full Text PDFThe formation of the autophagic vesicles requires the recruitment of ubiquitin-like Atg8 proteins to the membrane of nascent autophagosomes. Seven Atg8 homologs are present in mammals, split into the LC3 and the GABARAP/GATE-16 families, whose respective functions are unknown. Using Caenorhabditis elegans, we investigated the functions of the GABARAP and the LC3 homologs, LGG-1 and LGG-2, in autophagosome biogenesis.
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