Département de Pathologie et Biologie Cellulaire, Université de Montréal, C.P. 6128, Succursale centre-ville, Montréal, QC H3C 3J7, Canada.
Montreal Neurological Institute, McGill University, 3801 University Avenue, Montreal, QC H3A 2B4, Canada.
Cell. 2016 Jul 14;166(2):314-327. doi: 10.1016/j.cell.2016.05.039. Epub 2016 Jun 23.
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.
抗原呈递对于建立免疫耐受以及对于抗感染和癌症的免疫反应至关重要。尽管抗原呈递可以通过自噬介导,但在这里我们展示了一种依赖于线粒体来源的囊泡(MDV)的生成和运输而不是自噬/线粒体自噬的线粒体抗原呈递(MitAP)途径。我们发现,与帕金森病(PD)相关的两种线粒体蛋白 PINK1 和 Parkin 积极抑制 MDV 形成和 MitAP。在没有 PINK1 或 Parkin 的情况下,炎症条件会在体外和体内的免疫细胞中触发 MitAP。MitAP 和 MDV 的形成需要 Rab9 和分选连接蛋白 9,Parkin 抑制其向线粒体的募集。鉴定 PINK1 和 Parkin 作为炎症引发的免疫反应抑制途径的抑制剂,提示对 PD 病理学有了新的认识。