帕金
品脱1
粒体自噬
生物
自噬
细胞生物学
抗原呈递
线粒体
免疫系统
抗原
交叉展示
免疫学
疾病
帕金森病
遗传学
细胞凋亡
T细胞
病理
医学
作者
Diana Matheoud,Ayumu Sugiura,Angélique Bellemare‐Pelletier,Annie Laplante,Christiane Rondeau,Magali Chemali,Ali Fazel,John Bergeron,Louis‐Éric Trudeau,Yan Burelle,Étienne Gagnon,Heidi M. McBride,Michel Desjardins
出处
期刊:Cell
[Cell Press]
日期:2016-06-25
卷期号:166 (2): 314-327
被引量:570
标识
DOI:10.1016/j.cell.2016.05.039
摘要
Antigen presentation is essential for establishing immune tolerance and for immune responses against infectious disease and cancer. Although antigen presentation can be mediated by autophagy, here we demonstrate a pathway for mitochondrial antigen presentation (MitAP) that relies on the generation and trafficking of mitochondrial-derived vesicles (MDVs) rather than on autophagy/mitophagy. We find that PINK1 and Parkin, two mitochondrial proteins linked to Parkinson’s disease (PD), actively inhibit MDV formation and MitAP. In absence of PINK1 or Parkin, inflammatory conditions trigger MitAP in immune cells, both in vitro and in vivo. MitAP and the formation of MDVs require Rab9 and Sorting nexin 9, whose recruitment to mitochondria is inhibited by Parkin. The identification of PINK1 and Parkin as suppressors of an immune-response-eliciting pathway provoked by inflammation suggests new insights into PD pathology.
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