The STATs in cell stress-type responses

被引:38
作者
Dudley A.C. [1 ]
Thomas D. [2 ]
Best J. [1 ]
Jenkins A. [1 ]
机构
[1] The Department of Medicine, St. Vincent's Hospital, The University of Melbourne, Melbourne, VIC
[2] The Peter McCallum Cancer Center, Melbourne, VIC
关键词
Genistein; Cellular Stress; Serine Phosphorylation; Hyperosmotic Stress; Cell Survival Pathway;
D O I
10.1186/1478-811X-2-8
中图分类号
学科分类号
摘要
In the early 1990's, a new cell signaling pathway was described. This new paradigm, now known as the JAK/STAT pathway, has been extensively investigated in immune-type cells in response to interferons and interleukins. However, recent evidence suggests that the JAK/STAT pathway also mediates diverse cellular responses to various forms of biological stress including hypoxia/reperfusion, endotoxin, ultraviolet light, and hyperosmolarity. The current literature describing the JAK/STAT pathway's role in cellular stress responses has been reviewed herein, but it is clear that our knowledge in this area is far from complete. © 2004 Doudley et al; licensee BioMed Central Ltd.
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共 42 条
[1]  
Hardie D.G., Roles of the AMP-activated/SNF1 protein kinase family in the response to cellular stress, Biochem Soc Symp, 64, pp. 13-27, (1999)
[2]  
Minden A., Karin M., Regulation and function of the JNK subgroup of MAP kinases, Biochim Biophys Acta, 1333, (1997)
[3]  
Kisseleva T., Bhattacharya S., Braunstein J., Schindler C.W., Signaling through the JAK/STAT pathway, recent advances and future challenges, Gene, 285, pp. 1-24, (2002)
[4]  
Lim C.P., Cao X., Serine phosphorylation and negative regulation of Stat3 by JNK, J Biol Chem, 274, pp. 31055-31061, (1999)
[5]  
Kovarik P., Stoiber D., Eyers P.A., Menghini R., Neininger A., Gaestel M., Cohen P., Decker T., Stress-induced phosphorylation of STAT1 at Ser727 requires p38 mitogen-activated protein kinase whereas IFN-gamma uses a different signaling pathway, Proc Natl Acad Sci U S A, 96, pp. 13956-13961, (1999)
[6]  
Ramsauer K., Sadzak I., Porras A., Pilz A., Nebreda A.R., Decker T., Kovarik P., p38 MAPK enhances STAT1-dependent transcription independently of Ser-727 phosphorylation, Proc Natl Acad Sci U S A, 99, pp. 12859-12864, (2002)
[7]  
Maziere C., Dantin F., Dubois F., Santus R., Maziere J., Biphasic effect of UVA radiation on STAT1 activity and tyrosine phosphorylation in cultured human keratinocytes, Free Radic Biol Med, 28, pp. 1430-1437, (2000)
[8]  
McGinn S., Poronnik P., King M., Gallery E.D., Pollock C.A., High glucose and endothelial cell growth: Novel effects independent of autocrine TGF-beta 1 and hyperosmolarity, Am J Physiol Cell Physiol, 284, (2003)
[9]  
Mandarino L.J., Current hypotheses for the biochemical basis of diabetic retinopathy, Diabetes Care, 15, pp. 1892-1901, (1992)
[10]  
Nishikawa T., Edelstein D., Du X.L., Yamagishi S., Matsumura T., Kaneda Y., Yorek M.A., Beebe D., Oates P.J., Hammes H.P., Et al., Normalizing mitochondrial superoxide production blocks three pathways of hyperglycaemic damage, Nature, 404, pp. 787-790, (2000)