| Literature DB >> 23880766 |
Junichi Seino1, Li Wang, Yoichiro Harada, Chengcheng Huang, Kumiko Ishii, Noboru Mizushima, Tadashi Suzuki.
Abstract
Macroautophagy is an essential, homeostatic process involving degradation of a cell's own components; it plays a role in catabolizing cellular components, such as protein or lipids, and damaged or excess organelles. Here, we show that in Atg5(-/-) cells, sialyloligosaccharides specifically accumulated in the cytosol. Accumulation of these glycans was observed under non-starved conditions, suggesting that non-induced, basal autophagy is essential for their catabolism. Interestingly, once accumulated in the cytosol, sialylglycans cannot be efficiently catabolized by resumption of the autophagic process, suggesting that functional autophagy is important for preventing sialyloligosaccharides from accumulating in the cytosol. Moreover, knockdown of sialin, a lysosomal transporter of sialic acids, resulted in a significant reduction of sialyloligosaccharides, implying that autophagy affects the substrate specificity of this transporter. This study thus provides a surprising link between basal autophagy and catabolism of N-linked glycans.Entities:
Keywords: Autophagy; Glycan Catabolism; Glycoprotein; Lysosomal Glycoproteins; Lysosomes; Oligosaccharide; Sialic Acid; Sialin; Sialyloligosaccharides
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Year: 2013 PMID: 23880766 PMCID: PMC3772239 DOI: 10.1074/jbc.M113.464503
Source DB: PubMed Journal: J Biol Chem ISSN: 0021-9258 Impact factor: 5.157