| Literature DB >> 35000547 |
Valentina Millarte1, Martin Spiess1.
Abstract
Selective autophagy of damaged organelles assures maintenance of cellular homeostasis in eukaryotes. While the mechanisms by which cells selectively remove dysfunctional mitochondria, lysosomes, endoplasmic reticulum and other organelles has been well characterized, little is known about specific autophagy of damaged early endosomes. In our recent study, we uncovered a new role for RABEP1/Rabaptin5, a long-established regulator of early endosome function, in targeting the autophagy machinery to early endosomes damaged by chloroquine or by internalized Salmonella via interaction with RB1CC1/FIP200 and ATG16L1.Entities:
Keywords: ATG16L1; FIP200; Rabaptin5; Salmonella; autophagy; early endosome
Mesh:
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Year: 2022 PMID: 35000547 PMCID: PMC9037546 DOI: 10.1080/15548627.2021.2021497
Source DB: PubMed Journal: Autophagy ISSN: 1554-8627 Impact factor: 16.016