Autophagy in T and B cell homeostasis Recycling for sustainable growth

被引:8
作者
Arnold, Johan [1 ]
Murera, Diane [1 ]
Arbogast, Florent [1 ]
Muller, Sylviane [1 ,2 ]
Gros, Frederic [1 ,3 ]
机构
[1] CNRS, Immunopathol & Chim Therapeut, Lab Excellence MEDALIS, Inst Biol Mol & Cellulaire, 15 Rue Descartes, F-67084 Strasbourg, France
[2] Univ Strasbourg, Inst Etud Avancees USIAS, Strasbourg, France
[3] Univ Strasbourg, Strasbourg, France
来源
M S-MEDECINE SCIENCES | 2016年 / 32卷 / 03期
关键词
SYSTEMIC-LUPUS-ERYTHEMATOSUS; MHC CLASS-II; ANTIGEN PRESENTATION; INFLUENZA INFECTION; CENTRAL TOLERANCE; GENE ATG5; LYMPHOCYTES; MACROAUTOPHAGY; PROTEINS; SURVIVAL;
D O I
10.1051/medsci/20163203013
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
100103 [病原生物学]; 100218 [急诊医学];
摘要
Macroautophagy often abbreviated by "autophagy" is an intracellular degradation mechanism linked to lysosomal activity. Autophagy is conserved from yeast to mammals and plays a role in the response to energetic stress and in organelle homeostasis. Autophagy is also involved in the regulation of immunity, in particular in the adaptive immune response, which involves B and T lymphocytes. It was indeed shown that autophagy impacts the development of B and T cells as well as the education of T cells in the thymus. Autophagy also modulates activation, survival and polarization of T cells. It plays a role in antigen presentation by B cells, and in their TLR-mediated activation, and thus likely in their initial activation. Finally, autophagy is required for the survival of memory lymphocytes and effector cells like antibody-producing plasma cells. Interestingly, autophagy is deregulated in several autoimmune pathologies. The modulation of this phenomenon could possibly lead to new treatments aiming at limiting lymphocyte activation driving these pathologies. © 2016 médecine/sciences-Inserm.
引用
收藏
页码:281 / 289
页数:9
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