TY - JOUR
T1 - Autophagy genes in immunity
AU - Virgin, Herbert W.
AU - Levine, Beth
N1 - Funding Information:
We thank A. Diehl for medical illustration. Supported by the US National Institutes of Health (R01 CA074730, R01 CA096511, R01 AI054483, R01 AI065982 and U54 AI057160 to H.W.V., and R01 AI151267 and R01 CA109618 to B.L.), the Howard Hughes Medical Institute (B.L.) and the Ellison Medical Foundation (B.L.).
PY - 2009
Y1 - 2009
N2 - In its classical form, autophagy is a pathway by which cytoplasmic constituents, including intracellular pathogens, are sequestered in a double-membrane-bound autophagosome and delivered to the lysosome for degradation. This pathway has been linked to diverse aspects of innate and adaptive immunity, including pathogen resistance, production of type I interferon, antigen presentation, tolerance and lymphocyte development, as well as the negative regulation of cytokine signaling and inflammation. Most of these links have emerged from studies in which genes encoding molecules involved in autophagy are inactivated in immune effector cells. However, it is not yet known whether all of the critical functions of such genes in immunity represent 'classical autophagy' or possible as-yet-undefined autophagolysosome-independent functions of these genes. This review summarizes phenotypes that result from the inactivation of autophagy genes in the immune system and discusses the pleiotropic functions of autophagy genes in immunity.
AB - In its classical form, autophagy is a pathway by which cytoplasmic constituents, including intracellular pathogens, are sequestered in a double-membrane-bound autophagosome and delivered to the lysosome for degradation. This pathway has been linked to diverse aspects of innate and adaptive immunity, including pathogen resistance, production of type I interferon, antigen presentation, tolerance and lymphocyte development, as well as the negative regulation of cytokine signaling and inflammation. Most of these links have emerged from studies in which genes encoding molecules involved in autophagy are inactivated in immune effector cells. However, it is not yet known whether all of the critical functions of such genes in immunity represent 'classical autophagy' or possible as-yet-undefined autophagolysosome-independent functions of these genes. This review summarizes phenotypes that result from the inactivation of autophagy genes in the immune system and discusses the pleiotropic functions of autophagy genes in immunity.
UR - http://www.scopus.com/inward/record.url?scp=65249108735&partnerID=8YFLogxK
U2 - 10.1038/ni.1726
DO - 10.1038/ni.1726
M3 - Review article
C2 - 19381141
AN - SCOPUS:65249108735
SN - 1529-2908
VL - 10
SP - 461
EP - 470
JO - Nature immunology
JF - Nature immunology
IS - 5
ER -