坏死
程序性细胞死亡
自噬
细胞凋亡
细胞生物学
卡尔帕因
神经退行性变
生物
活性氧
蛋白质水解
医学
病理
生物化学
遗传学
疾病
酶
作者
Pierre Golstein,Guido Kroemer
标识
DOI:10.1016/j.tibs.2006.11.001
摘要
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.
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