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PMID: 10807318 Published · ppublish English Journal Article Review

MAP kinase pathways activated by stress: the p38 MAPK pathway.

Critical care medicine ·Vol. 28 ·No. 4 Suppl ·2000-04-00 ·Pages N67-77

Obata T, Brown GE, Yaffe MB

Abstract

A stress-activated serine/threonine protein kinase, p38 mitogen-activated protein kinase (p38 MAPK), belongs to the MAP kinase superfamily. Diverse extracellular stimuli, including ultraviolet light, irradiation, heat shock, high osmotic stress, proinflammatory cytokines and certain mitogens, trigger a stress-regulated protein kinase cascade culminating in activation of p38 MAPK through phosphorylation on a TGY motif within the kinase activation loop. p38 MAPK appears to play a major role in apoptosis, cytokine production, transcriptional regulation, and cytoskeletal reorganization, and has been causally implicated in sepsis, ischemic heart disease, arthritis, human immunodeficiency virus infection, and Alzheimer's disease. The availability of specific inhibitors helps to clarify the role that p38 MAPK plays in these processes, and may ultimately offer therapeutic benefit for certain critically ill patients.

MeSH Terms
Apoptosis/physiology Critical Illness Enzyme Inhibitors/pharmacology Humans MAP Kinase Signaling System/physiology Mitogen-Activated Protein Kinases/antagonists & inhibitors,physiology Stress, Physiological/physiopathology Transcription, Genetic/physiology p38 Mitogen-Activated Protein Kinases
Chemicals
Enzyme Inhibitors Mitogen-Activated Protein Kinases p38 Mitogen-Activated Protein Kinases
Authors & Affiliations
3 authors, click to expand affiliations / ORCID
Obata T
Department of Medicine, Beth Israel Deaconess Medical Center, Boston, MA, USA.
Brown G E
Yaffe M B
Article Info
Journal
Critical care medicine
Abbr.
Crit Care Med
ISSN
0090-3493
Published
2000-04-00
Pages
N67-77
Language
English
Region
United States
NLM ID
0355501
Subset
IM
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