In Vivo Requirement for Atg5 in Antigen Presentation by Dendritic Cells

被引:392
作者
Lee, Heung Kyu [1 ]
Mattei, Lisa M. [1 ]
Steinberg, Benjamin E. [2 ,3 ]
Alberts, Philipp [1 ]
Lee, Yun Hee [1 ]
Chervonsky, Alexander [5 ]
Mizushima, Noboru [6 ]
Grinstein, Sergio [2 ,4 ]
Iwasaki, Akiko [1 ]
机构
[1] Yale Univ, Sch Med, Dept Immunobiol, New Haven, CT 06520 USA
[2] Hosp Sick Children, Cell Biol Program, Toronto, ON M5G 1X8, Canada
[3] Univ Toronto, Inst Med Sci, Toronto, ON M5S 1A8, Canada
[4] Univ Toronto, Dept Biochem, Toronto, ON M5S 1A8, Canada
[5] Univ Chicago, Dept Pathol, Chicago, IL 60637 USA
[6] Tokyo Med & Dent Univ, Dept Physiol & Cell Biol, Tokyo 1138519, Japan
关键词
HERPES-SIMPLEX-VIRUS; CLASS-II MOLECULES; CD4(+) T-CELLS; RESTRICTED PRESENTATION; DIFFERENTIAL ROLES; CROSS-PRESENTATION; ADAPTIVE IMMUNITY; AUTOPHAGY PROTEIN; CYTOSOLIC ANTIGEN; TYPE-2; INFECTION;
D O I
10.1016/j.immuni.2009.12.006
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Autophagy is known to be important in presentation of cytosolic antigens on MHC class II (MHC II). However, the role of autophagic process in antigen presentation in vivo is unclear. Mice with dendritic cell (DC)-conditional deletion in Atg5, a key autophagy gene, showed impaired CD4(+) T cell priming after herpes simplex virus infection and succumbed to rapid disease. The most pronounced defect of Atg5(-/-) DCs was the processing and presentation of phagocytosed antigens containing Toll-like receptor stimuli for MHC class II. In contrast, cross-presentation of peptides on MHC I was intact in the absence of Atg5. Although induction of metabolic autophagy did not enhance MHC II presentation, autophagic machinery was required for optimal phagosome-to-lysosome fusion and subsequent processing of antigen for MHC II loading. Thus, our study revealed that DCs utilize autophagic machinery to optimally process and present extracellular microbial antigens for MHC II presentation.
引用
收藏
页码:227 / 239
页数:13
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