TY - JOUR
T1 - Regulation of mammalian autophagy in physiology and pathophysiology.
AU - Ravikumar, Brinda
AU - Sarkar, Sovan
AU - Davies, Janet E.
AU - Futter, Marie
AU - Garcia-Arencibia, Moises
AU - Green-Thompson, Zeyn W.
AU - Jimenez-Sanchez, Maria
AU - Korolchuk, Viktor I.
AU - Lichtenberg, Maike
AU - Luo, Shouqing
AU - Massey, Dunecan C.O.
AU - Menzies, Fiona M.
AU - Moreau, Kevin
AU - Narayanan, Usha
AU - Renna, Maurizio
AU - Siddiqi, Farah H.
AU - Underwood, Benjamin R.
AU - Winslow, AR
AU - Rubinsztein, David C.
PY - 2010/10
Y1 - 2010/10
N2 - (Macro)autophagy is a bulk degradation process that mediates the clearance of long-lived proteins and organelles. Autophagy is initiated by double-membraned structures, which engulf portions of cytoplasm. The resulting autophagosomes ultimately fuse with lysosomes, where their contents are degraded. Although the term autophagy was first used in 1963, the field has witnessed dramatic growth in the last 5 years, partly as a consequence of the discovery of key components of its cellular machinery. In this review we focus on mammalian autophagy, and we give an overview of the understanding of its machinery and the signaling cascades that regulate it. As recent studies have also shown that autophagy is critical in a range of normal human physiological processes, and defective autophagy is associated with diverse diseases, including neurodegeneration, lysosomal storage diseases, cancers, and Crohn's disease, we discuss the roles of autophagy in health and disease, while trying to critically evaluate if the coincidence between autophagy and these conditions is causal or an epiphenomenon. Finally, we consider the possibility of autophagy upregulation as a therapeutic approach for various conditions.
AB - (Macro)autophagy is a bulk degradation process that mediates the clearance of long-lived proteins and organelles. Autophagy is initiated by double-membraned structures, which engulf portions of cytoplasm. The resulting autophagosomes ultimately fuse with lysosomes, where their contents are degraded. Although the term autophagy was first used in 1963, the field has witnessed dramatic growth in the last 5 years, partly as a consequence of the discovery of key components of its cellular machinery. In this review we focus on mammalian autophagy, and we give an overview of the understanding of its machinery and the signaling cascades that regulate it. As recent studies have also shown that autophagy is critical in a range of normal human physiological processes, and defective autophagy is associated with diverse diseases, including neurodegeneration, lysosomal storage diseases, cancers, and Crohn's disease, we discuss the roles of autophagy in health and disease, while trying to critically evaluate if the coincidence between autophagy and these conditions is causal or an epiphenomenon. Finally, we consider the possibility of autophagy upregulation as a therapeutic approach for various conditions.
KW - Animals
KW - Autophagy
KW - Eukaryotic Cells
KW - Humans
KW - Mammals
KW - Phagosomes
KW - Signal Transduction
KW - Stress
KW - Physiological
U2 - 10.1152/physrev.00030.2009
DO - 10.1152/physrev.00030.2009
M3 - Article
SN - 1522-1210
VL - 90
SP - 1383
EP - 1435
JO - Physiol Rev
JF - Physiol Rev
IS - 4
ER -