Autophagy, immunity and human disease

被引:31
作者
Heath, Robert J. [2 ]
Xavier, Ramnik J. [1 ,2 ,3 ]
机构
[1] Harvard Univ, Massachusetts Gen Hosp, Sch Med, Ctr Computat & Integrat Biol,Richard B Simches Re, Boston, MA 02114 USA
[2] Harvard Univ, Massachusetts Gen Hosp, Sch Med, Gastrointestinal Unit,Ctr Inflammatory Bowel Dis, Boston, MA 02114 USA
[3] Broad Inst MIT & Harvard, Cambridge, MA USA
关键词
adaptive immunity; autophagy; Crohn's disease; innate immunity; GENOME-WIDE ASSOCIATION; CROHNS-DISEASE; SUSCEPTIBILITY LOCI; TUMOR-SUPPRESSOR; GENE ATG5; BECLIN; COMPLEX; LC3; MACROPHAGES; ATG16L1;
D O I
10.1097/MOG.0b013e32833104f1
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Purpose of review To give an overview of autophagy and its effects on innate and adaptive immunity and touch on some of the roles of autophagy in disease. Recent findings Precise regulation of autophagy is necessary to maintain metabolic equilibrium, immune homeostasis, delineate cell fate and influence host cell responses to cytosolic pathogens. A growing number of studies have implicated that inactivation of autophagy-selective responses contributes to inflammatory disorders, neurodegeneration and cancer, but the precise steps at which disease-associated autophagy-related (ATG) genes affect autophagy pathways is unknown at present. Summary In eukaryotic cells autophagy is constitutively active at low levels, whereas significant up-regulation occurs in response to a multitude of stresses. Autophagy has achieved notoriety as a perturbed biological process in many disease states and an exponential increase of studies attribute roles for autophagy in innate and adaptive immunity. Understanding how individual disease-associated ATG genes function will lead to a better understanding of and potentially novel therapies for treating the diseases in which they are involved.
引用
收藏
页码:512 / 520
页数:9
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