Developmentally programmed cell death in Drosophila

被引:61
作者
Denton, Donna [1 ,2 ,4 ]
Aung-Htut, May T. [1 ]
Kumar, Sharad [1 ,2 ,3 ,4 ]
机构
[1] Ctr Canc Biol, SA Pathol, Adelaide, SA 5000, Australia
[2] Univ Adelaide, Sch Mol & Biomed Sci, Adelaide, SA 5005, Australia
[3] Univ Adelaide, Dept Med, Adelaide, SA 5005, Australia
[4] Univ S Australia, Div Hlth Sci, Adelaide, SA 5001, Australia
来源
BIOCHIMICA ET BIOPHYSICA ACTA-MOLECULAR CELL RESEARCH | 2013年 / 1833卷 / 12期
基金
英国医学研究理事会;
关键词
Apoptosis; Autophagy; Caspases; Development; Drosophila; Programmed cell death; NEGATIVE BACTERIAL-INFECTION; STRESS-INDUCED APOPTOSIS; APICAL CASPASE DRONC; B FACTOR RELISH; CAENORHABDITIS-ELEGANS; CYTOCHROME-C; ECDYSONE RECEPTOR; NURSE CELLS; MELANOGASTER OOGENESIS; PROVIDES COMPETENCE;
D O I
10.1016/j.bbamcr.2013.06.014
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
During the development of metazoans, programmed cell death (PCD) is essential for tissue patterning, removal of unwanted cells and maintaining homeostasis. In the past 20 years Drosophila melanogaster has been one of the systems of choice for studies involving developmental cell death, providing an ideal genetically tractable model of intermediary complexity between Caenorhabditis elegans and mammals. The lessons learned from studies using Drosophila indicate both the conserved nature of the many cell death pathways as well as novel and unexpected mechanisms. In this article we review the understanding of PCD during Drosophila development, highlighting the key mechanisms that are evolutionarily conserved as well as apparently unusual pathways, which indicate divergence, but provide evidence of complexity acquired during organismic evolution. This article is part of a Special Section entitled: Cell Death Pathways. Guest Editors: Frank Madeo and Slaven Stekovic. (C) 2013 Elsevier B.V. All rights reserved.
引用
收藏
页码:3499 / 3506
页数:8
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