The mitochondrial death pathway: a promising therapeutic target in diseases

被引:215
作者
Gupta, Sanjeev [1 ,2 ]
Kass, George E. N. [3 ]
Szegezdi, Eva [1 ,2 ]
Joseph, Bertrand [4 ]
机构
[1] Natl Univ Ireland, Sch Nat Sci, Galway, Ireland
[2] Natl Univ Ireland, NCBES, Galway, Ireland
[3] Univ Surrey, Fac Med & Hlth Sci, Guildford GU2 5XH, Surrey, England
[4] Karolinska Inst, Dept Oncol Pathol, CCK, Stockholm, Sweden
关键词
mitochondrial permeability transition; apoptosis; Bcl-2; caspases; mitochondrial outer membrane permeabilization; PERMEABILITY TRANSITION PORE; CYTOCHROME-C RELEASE; ADENINE-NUCLEOTIDE TRANSLOCATOR; AMYOTROPHIC-LATERAL-SCLEROSIS; BCL-2; FAMILY-MEMBERS; SENSITIVE POTASSIUM CHANNELS; ETOPOSIDE-INDUCED APOPTOSIS; METASTATIC BREAST-CANCER; COMPRISE VDAC MOLECULES; DEPENDENT ANION CHANNEL;
D O I
10.1111/j.1582-4934.2009.00697.x
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
The mitochondrial pathway to apoptosis is a major pathway of physiological cell death in vertebrates. The mitochondrial cell death pathway commences when apoptogenic molecules present between the outer and inner mitochondrial membranes are released into the cytosol by mitochondrial outer membrane permeabilization ( MOMP). BCL-2 family members are the sentinels of MOMP in the mitochondrial apoptotic pathway; the pro-apoptotic B cell lymphoma (BCL)-2 proteins, BCL-2 associated x protein and BCL-2 antagonist killer 1 induce MOMP whereas the anti-apoptotic BCL-2 proteins, BCL-2, BCL-x(L) and myeloid cell leukaemia 1 prevent MOMP from occurring. The release of pro-apoptotic factors such as cytochrome c from mitochondria leads to formation of a multimeric complex known as the apoptosome and initiates caspase activation cascades. These pathways are important for normal cellular homeostasis and play key roles in the pathogenesis of many diseases. In this review, we will provide a brief overview of the mitochondrial death pathway and focus on a selection of diseases whose pathogenesis involves the mitochondrial death pathway and we will examine the various pharmacological approaches that target this pathway.
引用
收藏
页码:1004 / 1033
页数:30
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