Galais Mathilde, Pradel Baptiste, Vergne Isabelle, Robert-Hebmann Véronique, Espert Lucile, Biard-Piechaczyk Martine
Institut de recherche en infectiologie de Montpellier (IRIM), Université de Montpellier, CNRS, 1919, route de Mende, 34293 Montpellier, France.
Institut de pharmacologie et de biologie structurale (IPBS), Université de Toulouse, CNRS, UPS, 205, route de Narbonne, 31400 Toulouse, France.
Med Sci (Paris). 2019 Aug-Sep;35(8-9):635-642. doi: 10.1051/medsci/2019129. Epub 2019 Sep 18.
Phagocytosis and macroautophagy, named here autophagy, are two essential mechanisms of lysosomal degradation of diverse cargos into membrane structures. Both mechanisms are involved in immune regulation and cell survival. However, phagocytosis triggers degradation of extracellular material whereas autophagy engulfs only cytoplasmic elements. Furthermore, activation and maturation of these two processes are different. LAP (LC3-associated phagocytosis) is a form of phagocytosis that uses components of the autophagy pathway. It can eliminate (i) pathogens, (ii) immune complexes, (iii) threatening neighbouring cells, dead or alive, and (iv) cell debris, such as POS (photoreceptor outer segment) and the midbody released at the end of mitosis. Cells have thus optimized their means of elimination of dangerous components by sharing some fundamental elements coming from the two main lysosomal degradation pathways.
吞噬作用和巨自噬(本文中称为自噬)是将各种货物降解为膜结构的两种重要的溶酶体降解机制。这两种机制都参与免疫调节和细胞存活。然而,吞噬作用触发细胞外物质的降解,而自噬仅吞噬细胞质成分。此外,这两个过程的激活和成熟是不同的。LC3相关吞噬作用(LAP)是一种利用自噬途径成分的吞噬作用形式。它可以清除(i)病原体,(ii)免疫复合物,(iii)威胁相邻细胞,无论其死活,以及(iv)细胞碎片,如光感受器外段(POS)和有丝分裂末期释放的中间体。因此,细胞通过共享来自两种主要溶酶体降解途径的一些基本元件,优化了它们清除危险成分的方式。