TY - JOUR
T1 - Cell death by necrosis
T2 - towards a molecular definition
AU - Golstein, Pierre
AU - Kroemer, Guido
N1 - Funding Information:
P.G. is supported by the EU (Trans-death), INSERM, CNRS and ARC. G.K. is supported by a special grant from Ligue Nationale contre le Cancer, EU (Trans-Death, Death Train) and INSERM.
PY - 2007/1/1
Y1 - 2007/1/1
N2 - Necrosis has been defined as a type of cell death that lacks the features of apoptosis and autophagy, and is usually considered to be uncontrolled. Recent research suggests, however, that its occurrence and course might be tightly regulated. After signaling- or damage-induced lesions, necrosis can include signs of controlled processes such as mitochondrial dysfunction, enhanced generation of reactive oxygen species, ATP depletion, proteolysis by calpains and cathepsins, and early plasma membrane rupture. In addition, the inhibition of specific proteins involved in regulating apoptosis or autophagy can change the type of cell death to necrosis. Because necrosis is prominent in ischemia, trauma and possibly some forms of neurodegeneration, further biochemical comprehension and molecular definition of this process could have important clinical implications.
AB - Necrosis has been defined as a type of cell death that lacks the features of apoptosis and autophagy, and is usually considered to be uncontrolled. Recent research suggests, however, that its occurrence and course might be tightly regulated. After signaling- or damage-induced lesions, necrosis can include signs of controlled processes such as mitochondrial dysfunction, enhanced generation of reactive oxygen species, ATP depletion, proteolysis by calpains and cathepsins, and early plasma membrane rupture. In addition, the inhibition of specific proteins involved in regulating apoptosis or autophagy can change the type of cell death to necrosis. Because necrosis is prominent in ischemia, trauma and possibly some forms of neurodegeneration, further biochemical comprehension and molecular definition of this process could have important clinical implications.
UR - http://www.scopus.com/inward/record.url?scp=33846018602&partnerID=8YFLogxK
U2 - 10.1016/j.tibs.2006.11.001
DO - 10.1016/j.tibs.2006.11.001
M3 - Review article
C2 - 17141506
AN - SCOPUS:33846018602
SN - 0968-0004
VL - 32
SP - 37
EP - 43
JO - Trends in Biochemical Sciences
JF - Trends in Biochemical Sciences
IS - 1
ER -