Biogenesis and function of multivesicular bodies.
By Robert C. Piper, David J. Katzmann. Annual Review of Cell and Developmental Biology, 2007
792 citations recorded by the source corpus.
Subfields: Cell Biology, Epidemiology, Physiology
View Paper: https://www.semanticscholar.org/paper/916832cb474a39c072d6b96327fc27f66de4654a
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In Cell Biology
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In Epidemiology
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Citations in the corpus
- Exosome Function: From Tumor Immunology to Pathogen Biology (2008, background): “ESCRT-I, -II and -III recognize monoubiquitinated cargoes and promote their inclusion in MVBs (14).”
- Endosome maturation (2011, background): “These include the following (Mellman, 1996; Zerial and McBride, 2001; Maxfield and McGraw, 2004; Piper and Katzmann, 2007; Luzio et al, 2007b; van Meel and Klumperman, 2008; Woodman and Futter, 2008; Saftig and Klumperman, 2009; Jovic et al, 2010; Von Bartheld and Altick, 2011).”
- Post-translational modifications in signal integration (2010, background): “The ubiquitination of EGFR by c-Cbl and the recognition of this ubiquitin moiety by adaptor proteins in the endosomal sorting complex required for transport (ESCRT) complex acts as a signal to sort the receptor for degradatio”
- Molecular Mechanism of Multivesicular Body Biogenesis by ESCRT Complexes (2010, methodology): “(57 mol%), POPS (10 mol%), cholesterol (25 mol%), PI(3)P (3 mol%), Ni-”
- Biogenesis of extracellular vesicles (EV): exosomes, microvesicles, retrovirus-like vesicles, and apoptotic bodies (2013, positive): “For instance, actinmyosin interactions appear critical to the formation of all four types of EVs [66, 85, 100, 115].”
- Membrane Scission by the ESCRT-III Complex (2009, background): “When PtdIns(3)P was replaced by another endosomal phosphoinositide, phosphatidylinositol-3,5-bisphosphate (PtdIns(3,5)P2), the reaction proceeded just as with PtdIns(3)P (Supplementary Fig.”
- Mechanisms of regulated unconventional protein secretion (2009, background): “MVBs have well-characterized roles in receptor downregulation and protein degradatio”
- Membrane budding and scission by the ESCRT machinery: it's all in the neck (2010, neutral): “Late endosomes filled with ILVs are referred to as multivesicular bodies (MVBs) or sometimes multivesicular endosome”
- Molecular Biology of Hepatitis B Virus Infection (2015, neutral): “on proteins normally associated with the endosomal sorting complex required for transport (ESCRT) and with the formation of multivesicular bodies (MVPs) (Piper and Katzmann, 2007; Watanabe et al., 2007).”