Function of reactive oxygen species during animal development:: Passive or active?

被引:306
作者
Covarrubias, Luis [1 ]
Hernandez-Garcia, David [1 ]
Schnabel, Denhi [1 ]
Salas-Vidal, Enrique [1 ]
Castro-Obregon, Susana [1 ]
机构
[1] Univ Nacl Autonoma Mexico, Inst Biotechnol, Dept Dev Genet & Mol Physiol, Cuernavaca 62210, Morelos, Mexico
关键词
reactive oxygen species; superoxide; hydrogen peroxide; oxidative stress; antioxidants; redox regulation; signal transduction; proliferation; differentiation; apoptosis; pogrammed cell death; morphogenesis; development;
D O I
10.1016/j.ydbio.2008.04.041
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
Oxidative stress is considered causal of aging and pathological cell death, however, very little is known about its function in the natural processes that support the formation of an organism. It is generally thought that Cells most continuously protect themselves from the possible damage caused by reactive oxygen species (ROS) (passive ROS function). However, presently, ROS are recognized as physiologically relevant molecules that mediate cell responses to a variety of stimuli, and the activities of several molecules, some developmentally relevant, are directly or indirectly regulated by oxidative stress (active ROS function). Here we review recent data that are suggestive of specific ROS functions during development of animals, Particularly mammals. (C) 2008 Elsevier Inc. All rights reserved.
引用
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页码:1 / 11
页数:11
相关论文
共 181 条
[1]   Oxidative stress and gene regulation [J].
Allen, RG ;
Tresini, M .
FREE RADICAL BIOLOGY AND MEDICINE, 2000, 28 (03) :463-499
[2]   DIFFERENTIAL INCORPORATION OF FATTY-ACIDS INTO AND PEROXIDATIVE LOSS OF FATTY-ACIDS FROM PHOSPHOLIPIDS OF HUMAN SPERMATOZOA [J].
ALVAREZ, JG ;
STOREY, BT .
MOLECULAR REPRODUCTION AND DEVELOPMENT, 1995, 42 (03) :334-346
[3]   Reactive oxygen generated by Nox1 triggers the angiogenic switch [J].
Arbiser, JL ;
Petros, J ;
Klafter, R ;
Govindajaran, B ;
McLaughlin, ER ;
Brown, LF ;
Cohen, C ;
Moses, M ;
Kilroy, S ;
Arnold, RS ;
Lambeth, JD .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2002, 99 (02) :715-720
[4]  
Arthur JR, 2000, CELL MOL LIFE SCI, V57, P1825
[5]   Genetically encoded fluorescent indicator for intracellular hydrogen peroxide [J].
Belousov, VV ;
Fradkov, AF ;
Lukyanov, KA ;
Staroverov, DB ;
Shakhbazov, KS ;
Terskikh, AV ;
Lukyanov, S .
NATURE METHODS, 2006, 3 (04) :281-286
[6]   Focal adhesion kinase regulation by oxidative stress in different cell types [J].
Ben Mahdi, MH ;
Andrieu, V ;
Pasquier, C .
IUBMB LIFE, 2000, 50 (4-5) :291-299
[7]   A gradient of cytoplasmic Cactus degradation establishes the nuclear localization gradient of the dorsal morphogen in Drosophila [J].
Bergmann, A ;
Stein, D ;
Geisler, R ;
Hagenmaier, S ;
Schmid, B ;
Fernandez, N ;
Schnell, B ;
NussleinVolhard, C .
MECHANISMS OF DEVELOPMENT, 1996, 60 (01) :109-123
[8]   Specific aquaporins facilitate the diffusion of hydrogen peroxide across membranes [J].
Bienert, Gerd P. ;
Moller, Anders L. B. ;
Kristiansen, Kim A. ;
Schulz, Alexander ;
Moller, Ian M. ;
Schjoerring, Jan K. ;
Jahn, Thomas P. .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2007, 282 (02) :1183-1192
[9]   Programmed cell death via mitochondria: Different modes of dying [J].
Bras, M ;
Queenan, B ;
Susin, SA .
BIOCHEMISTRY-MOSCOW, 2005, 70 (02) :231-+
[10]   Loss of Aif function causes cell death in the mouse embryo, but the temporal progression of patterning is normal [J].
Brown, Doris ;
Yu, Benjamin D. ;
Joza, Nicholas ;
Benit, Paule ;
Meneses, Juanito ;
Firpo, Meri ;
Rustin, Pierre ;
Penninger, Josef M. ;
Martin, Gail R. .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2006, 103 (26) :9918-9923