Integrated activation of MAP3Ks balances cell fate in response to stress.
| Autor: | Winter-Vann AM; Department of Pharmacology, 1108 Mary Ellen Jones Bldg, Campus Box 7365, University of North Carolina School of Medicine, Chapel Hill, North Carolina 27599-7365, USA., Johnson GL |
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| Jazyk: | angličtina |
| Zdroj: | Journal of cellular biochemistry [J Cell Biochem] 2007 Nov 01; Vol. 102 (4), pp. 848-58. |
| DOI: | 10.1002/jcb.21522 |
| Abstrakt: | In vivo, tissues and organs are exposed to numerous stressors that require cells to respond appropriately for viability and homeostasis. Cells respond to these stressors, which range from UV irradiation, heat shock, chemicals, and changes in osmolality, to oxidative stress and inflammatory cytokines, by activating pathways that protect cells from damage. If the stress is too great, cells commit to undergo apoptosis. Such cell fate decisions involve the stress-mediated activation of mitogen-activated protein kinase (MAPK) networks, ultimately under the control of MAPK kinase kinases, or MAP3Ks. It is the MAP3Ks that coordinate the localization, duration and magnitude of MAPK activation in response to cell stress. A single stressor may activate several MAP3Ks, each of which impacts the balance between survival and apoptotic signaling. In this prospect article, we review the specific MAP3Ks that integrate the physiological response to cell stressors. The interrelationships among different stressors are discussed, with an emphasis on how the balance of signaling through MAP3Ks controls the MAPK response to determine cell fate. ((c) 2007 Wiley-Liss, Inc.) |
| Databáze: | MEDLINE |
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