MAMMALIAN MAPK SIGNAL TRANSDUCTION PATHWAYS ACTIVATED BY STRESS AND INFLAMMATION: A 10-YEAR UPDATE

被引:1171
作者
Kyriakis, John M. [1 ]
Avruch, Joseph
机构
[1] Tufts Med Ctr, Mol Cardiol Res Inst, Dept Med, Boston, MA 02111 USA
关键词
TUMOR-NECROSIS-FACTOR; N-TERMINAL KINASE; JUN NH2-TERMINAL KINASE; GERMINAL CENTER KINASE; TOLL-LIKE RECEPTORS; T-CELL-ACTIVATION; HEMATOPOIETIC PROGENITOR KINASE; EMBRYONIC CARDIOVASCULAR DEVELOPMENT; PATTERN-RECOGNITION RECEPTORS; STE20-RELATED PROTEIN-KINASE;
D O I
10.1152/physrev.00028.2011
中图分类号
Q4 [生理学];
学科分类号
071003 ;
摘要
Kyriakis JM, Avruch J. Mammalian MAPK Signal Transduction Pathways Activated by Stress and Inflammation: A 10-Year Update. Physiol Rev 92: 689-737, 2012; doi:10.1152/physrev.00028.2011.-The mammalian stress-activated families of mitogen-activated protein kinases (MAPKs) were first elucidated in 1994, and by 2001, substantial progress had been made in identifying the architecture of the pathways upstream of these kinases as well as in cataloguing candidate substrates. This information remains largely sound. Nevertheless, an informed understanding of the physiological and pathophysiological roles of these kinases remained to be accomplished. In the past decade, there has been an explosion of new work using RNAi in cells, as well as transgenic, knockout and conditional knockout technology in mice that has provided valuable insight into the functions of stress-activated MAPK pathways. These findings have important implications in our understanding of organ development, innate and acquired immunity, and diseases such as atherosclerosis, tumorigenesis, and type 2 diabetes. These new developments bring us within striking distance of the development and validation of novel treatment strategies. Herein we first summarize the molecular components of the mammalian stress-regulated MAPK pathways and their regulation as described thus far. We then review some of the in vivo functions of these pathways.
引用
收藏
页码:689 / 737
页数:49
相关论文
共 351 条
[1]   Essential role of p38α MAP kinase in placental but not embryonic cardiovascular development [J].
Adams, RH ;
Porras, A ;
Alonso, G ;
Jones, M ;
Vintersten, K ;
Panelli, S ;
Valladares, A ;
Perez, L ;
Klein, R ;
Nebreda, AR .
MOLECULAR CELL, 2000, 6 (01) :109-116
[2]   Phosphorylation of Ser307 in insulin receptor substrate-1 blocks interactions with the insulin receptor and inhibits insulin action [J].
Aguirre, V ;
Werner, ED ;
Giraud, J ;
Lee, YH ;
Shoelson, SE ;
White, MF .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2002, 277 (02) :1531-1537
[3]   The c-Jun NH2-terminal kinase promotes insulin resistance during association with insulin receptor substrate-1 and phosphorylation of Ser307 [J].
Aguirre, V ;
Uchida, T ;
Yenush, L ;
Davis, R ;
White, MF .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2000, 275 (12) :9047-9054
[4]   Hematopoietic Progenitor Kinase 1 Is a Negative Regulator of Dendritic Cell Activation [J].
Alzabin, Saba ;
Bhardwaj, Nina ;
Kiefer, Friedemann ;
Sawasdikosol, Sansana ;
Burakoff, Steven .
JOURNAL OF IMMUNOLOGY, 2009, 182 (10) :6187-6194
[5]   SH2/SH3 adaptor proteins can link tyrosine kinases to a Ste20-related protein kinase, HPK1 [J].
Anafi, M ;
Kiefer, F ;
Gish, GD ;
Mbamalu, G ;
Iscove, NN ;
Pawson, T .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1997, 272 (44) :27804-27811
[6]   The kinases MSK1 and MSK2 act as negative regulators of Toll-like receptor signaling [J].
Ananieva, Olga ;
Darragh, Joanne ;
Johansen, Claus ;
Carr, Julia M. ;
McIlrath, Joanne ;
Park, Jin Mo ;
Wingate, Andrew ;
Monk, Claire E. ;
Toth, Rachel ;
Santos, Susana G. ;
Iversen, Lars ;
Arthur, J. Simon C. .
NATURE IMMUNOLOGY, 2008, 9 (09) :1028-1036
[7]  
Arch RH, 2000, GENE DEV, V12, P2821
[8]   The specificities of protein kinase inhibitors: an update [J].
Bain, J ;
McLauchlan, H ;
Elliott, M ;
Cohen, P .
BIOCHEMICAL JOURNAL, 2003, 371 :199-204
[9]   The selectivity of protein kinase inhibitors: a further update [J].
Bain, Jenny ;
Plater, Lorna ;
Elliott, Matt ;
Shpiro, Natalia ;
Hastie, C. James ;
Mclauchlan, Hilary ;
Klevernic, Iva ;
Arthur, J. Simon C. ;
Alessi, Dario R. ;
Cohen, Philip .
BIOCHEMICAL JOURNAL, 2007, 408 :297-315
[10]   Signaling by proinflammatory cytokines: oligomerization of TRAF2 and TRAF6 is sufficient for JNK and IKK activation and target gene induction via an amino-terminal effector domain [J].
Baud, V ;
Liu, ZG ;
Bennett, B ;
Suzuki, N ;
Xia, Y ;
Karin, M .
GENES & DEVELOPMENT, 1999, 13 (10) :1297-1308