CHMP5 is essential for late endosome function and down-regulation of receptor signaling during mouse embryogenesis |
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| Authors: | Shim Jae-Hyuck Xiao Changchun Hayden Matthew S Lee Ki-Young Trombetta E Sergio Pypaert Marc Nara Atsuki Yoshimori Tamotsu Wilm Bettina Erdjument-Bromage Hediye Tempst Paul Hogan Brigid L M Mellman Ira Ghosh Sankar |
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| Affiliation: | Section of Immunobiology, Ludwig Institute for Cancer Research, Yale University School of Medicine, New Haven, CT 06520, USA. |
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| Abstract: | Charged MVB protein 5 (CHMP5) is a coiled coil protein homologous to the yeast Vps60/Mos10 gene and other ESCRT-III complex members, although its precise function in either yeast or mammalian cells is unknown. We deleted the CHMP5 gene in mice, resulting in a phenotype of early embryonic lethality, reflecting defective late endosome function and dysregulation of signal transduction. Chmp5-/- cells exhibit enlarged late endosomal compartments that contain abundant internal vesicles expressing proteins that are characteristic of late endosomes and lysosomes. This is in contrast to ESCRT-III mutants in yeast, which are defective in multivesicular body (MVB) formation. The degradative capacity of Chmp5-/- cells was reduced, and undigested proteins from multiple pathways accumulated in enlarged MVBs that failed to traffic their cargo to lysosomes. Therefore, CHMP5 regulates late endosome function downstream of MVB formation, and the loss of CHMP5 enhances signal transduction by inhibiting lysosomal degradation of activated receptors. |
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