| Literature DB >> 20673754 |
Keiichi Tamai1, Nobuyuki Tanaka, Takashi Nakano, Eiji Kakazu, Yasuteru Kondo, Jun Inoue, Masaaki Shiina, Koji Fukushima, Tomoaki Hoshino, Kouichi Sano, Yoshiyuki Ueno, Tooru Shimosegawa, Kazuo Sugamura.
Abstract
Exosomes are nanovesicles derived from multivesicular bodies (MVBs) in antigen-presenting cells. The components of the ESCRT (endosomal sorting complex required for transport) pathway are critical for the formation of MVBs, however the relationship between the ESCRT pathway and the secretion of exosomes remains unclear. We here demonstrate that Hrs, an ESCRT-0 protein, is required for fascilitating the secretion of exosomes in dendritic cells (DCs). Ultrastructural analyses showed typical saucer-shaped exosomes in the culture supernatant from both the control and Hrs-depleted DCs. However, the amount of exosome secretion was significantly decreased in Hrs-depleted DCs following stimulations with ovalbumin (OVA) as well as calcium ionophore. Antigen-presentation activity was also suppressed in exsosomes purified from Hrs-depleted DCs, while no alteration in OVA degradation was seen in Hrs-depleted DCs. These data indicated that Hrs is involved in the regulation of antigen-presentation activity through the exosome secretion. Copyright 2010 Elsevier Inc. All rights reserved.Entities:
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Year: 2010 PMID: 20673754 DOI: 10.1016/j.bbrc.2010.07.083
Source DB: PubMed Journal: Biochem Biophys Res Commun ISSN: 0006-291X Impact factor: 3.575