Anti-apoptotic BCL-2 family members in development

被引:290
作者
Opferman, Joseph T. [1 ]
Kothari, Anisha [1 ]
机构
[1] St Jude Childrens Res Hosp, Dept Cell & Mol Biol, 262 Danny Thomas Pl,MS 340, Memphis, TN 38105 USA
基金
英国科研创新办公室;
关键词
PROGRAMMED CELL-DEATH; ANTIAPOPTOTIC MCL-1; POLYCYSTIC KIDNEY; NERVOUS-SYSTEM; IN-VIVO; SURVIVAL; EXPRESSION; PROTEIN; NEURONS; GENE;
D O I
10.1038/cdd.2017.170
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Almost 30 years ago it was first appreciated that anti-apoptotic B-cell lymphoma-2 (BCL-2) prevents the induction of apoptosis not only in malignant cells, but also in normal cellular lineages. This critical observation has rapidly evolved from merely identifying new BCL-2 family members to understanding how their biochemical interactions trigger the cell death process, and, more recently, to pharmacological inhibition of anti-apoptotic BCL-2 function in disease. Indeed, the proper regulation of apoptosis is important in many aspects of life including development, homeostasis, and disease biology. To better understand these processes, scientists have used many tools to assess the contribution of individual anti-apoptotic BCL-2 family members. This review will focus on the prominent roles for BCL-2 and other pro-survival family members in promoting the development of mammals during early embryogenesis, neurogenesis, and hematopoiesis.
引用
收藏
页码:37 / 45
页数:9
相关论文
共 85 条
[1]   BCL-2 GENE IS HIGHLY EXPRESSED DURING NEUROGENESIS IN THE CENTRAL-NERVOUS-SYSTEM [J].
ABEDOHMAE, S ;
HARADA, N ;
YAMADA, K ;
TANAKA, R .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1993, 191 (03) :915-921
[2]   Interleukin-2 receptor common gamma-chain signaling cytokines regulate activated T cell apoptosis in response to growth factor withdrawal: Selective induction of anti-apoptotic (bcl-2, bcl-x(L)) but not pro-apoptotic (bax, bcl-x(S)) gene expression [J].
Akbar, AN ;
Borthwick, NJ ;
Wickremasinghe, RG ;
Panayiotidis, P ;
Pilling, D ;
Bofill, M ;
Krajewski, S ;
Reed, JC ;
Salmon, M .
EUROPEAN JOURNAL OF IMMUNOLOGY, 1996, 26 (02) :294-299
[3]   THE PROTOONCOGENE BCL-2 CAN SELECTIVELY RESCUE NEUROTROPHIC FACTOR-DEPENDENT NEURONS FROM APOPTOSIS [J].
ALLSOPP, TE ;
WYATT, S ;
PATERSON, HF ;
DAVIES, AM .
CELL, 1993, 73 (02) :295-307
[4]   Mcl-1 is a key regulator of apoptosis during CNS development and after DNA damage [J].
Arbour, Nicole ;
Vanderluit, Jacqueline L. ;
Le Grand, J. Nicole ;
Jahani-Asl, Arezu ;
Ruzhynsky, Vladimir A. ;
Cheung, Eric C. C. ;
Kelly, Melissa A. ;
MacKenzie, Alexander E. ;
Park, David S. ;
Opferman, Joseph T. ;
Slack, Ruth S. .
JOURNAL OF NEUROSCIENCE, 2008, 28 (24) :6068-6078
[5]   Thrombopoietin, but not erythropoietin promotes viability and inhibits apoptosis of multipotent murine hematopoietic progenitor cells in vitro [J].
Borge, OJ ;
Ramsfjell, V ;
Veiby, OP ;
Murphy, MJ ;
Lok, S ;
Jacobsen, SEW .
BLOOD, 1996, 88 (08) :2859-2870
[6]   Degenerative disorders caused by Bcl-2 deficiency prevented by loss of its BH3-only antagonist bim [J].
Bouillet, P ;
Cory, S ;
Zhang, LC ;
Strasser, A ;
Adams, JM .
DEVELOPMENTAL CELL, 2001, 1 (05) :645-653
[7]   Developmental Regulated Expression of Anti- and Pro-Apoptotic BCL-2 Family Genes During Human Early Embryonic Development [J].
Boumela, I. ;
Assou, S. ;
Haouzi, D. ;
Dechaud, H. ;
Ait-Ahmed, O. ;
Hamamah, S. .
CURRENT MEDICINAL CHEMISTRY, 2014, 21 (11) :1361-1369
[8]   Constitutive death of platelets leading to scavenger receptor-mediated phagocytosis - A caspase-independent cell clearance program [J].
Brown, SB ;
Clarke, MCH ;
Magowan, L ;
Sanderson, H ;
Savill, J .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2000, 275 (08) :5987-5996
[9]   mcl-1 is an immediate-early gene activated by the granulocyte-macrophage colony-stimulating factor (GM-CSF) signaling pathway and is one component of the GM-CSF viability response [J].
Chao, JR ;
Wang, JM ;
Lee, SF ;
Peng, HW ;
Lin, YH ;
Chou, CH ;
Li, JC ;
Huang, HM ;
Chou, CK ;
Kuo, ML ;
Yen, JJY ;
Yang-Yen, HF .
MOLECULAR AND CELLULAR BIOLOGY, 1998, 18 (08) :4883-4898
[10]   The BCL-2 Family Reunion [J].
Chipuk, Jerry E. ;
Moldoveanu, Tudor ;
Llambi, Fabien ;
Parsons, Melissa J. ;
Green, Douglas R. .
MOLECULAR CELL, 2010, 37 (03) :299-310