Département de pathologie et biologie cellulaire, Université de Montréal, Montreal, Canada.
Cell Mol Life Sci. 2011 May;68(9):1533-41. doi: 10.1007/s00018-011-0660-3. Epub 2011 Mar 10.
The classical view that endogenous antigens are processed by the proteasome and loaded on MHC class I molecules in the endoplasmic reticulum, while exogenous antigens taken up by endocytosis or phagocytosis are degraded and loaded on MHC class II in lysosome-derived organelles, has evolved along with the improvement of our understanding of the cell biology of antigen-presenting cells. In recent years, evidence for alternative presentation pathways has emerged. Exogenous antigens can be processed by the proteasome and loaded on MHC class I through a pathway called cross-presentation. Moreover, endogenous antigens can be targeted to lytic organelles for presentation on MHC class II through autophagy, a highly conserved cellular process of self-eating. Recent evidence indicates that the vacuolar degradation of endogenous antigens is also beneficial for presentation on MHC class I molecules. This review focuses on how various forms of autophagy participate to presentation of these antigens on MHC class I.
经典观点认为,内源性抗原在细胞质中通过蛋白酶体处理并加载到 MHC I 类分子上,而通过胞吞作用或吞噬作用摄取的外源性抗原在溶酶体衍生的细胞器中降解并加载到 MHC II 类分子上,这一观点随着人们对抗原呈递细胞的细胞生物学理解的提高而不断发展。近年来,出现了替代呈递途径的证据。外源性抗原可以通过一种称为交叉呈递的途径通过蛋白酶体处理并加载到 MHC I 类分子上。此外,内源性抗原可以通过自噬(一种高度保守的自我吞噬的细胞过程)靶向溶酶体进行 MHC II 类分子的呈递。最近的证据表明,内源性抗原的液泡降解也有利于 MHC I 类分子的呈递。这篇综述重点介绍了各种形式的自噬如何参与这些抗原在 MHC I 类分子上的呈递。