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Cell Immunol. 1997 Sep 15;180(2):116-23.

The p38 mitogen-activated protein kinase pathway in activated and anergic Th1 cells.

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1
Inflammatory Diseases Research, Dupont Merck Pharmaceutical Company, Wilmington, Delaware 19880-0400, USA.

Abstract

Stimulation of T cells through the TCR leads to activation of the mitogen-activated protein kinase (MAPK) family members ERK (extracellular signal-regulated kinase) and JNK (jun NH2-terminal kinase). These kinases act in synergy to increase the activity of the transcription factor AP-1 which is involved in the transcriptional upregulation of IL-2. Recently a third MAPK member, p38, has been identified. The effects of T cell activation on this pathway have not yet been elucidated. Using two murine Th1 clones, we demonstrate that the p38 pathway is induced upon anti-CD3 plus anti-CD28 crosslinking or PMA plus ionomycin stimulation. p38 activity was induced fully by anti-CD3 or PMA alone and is not enhanced by costimulation even at low levels of TCR signaling. p38 activity peaked at 20 min and was significantly decreased by 2 hr. Anergic (tolerant) Th1 cells showed decreased p38 activity as well as decreased ERK and JNK activities even though levels of these proteins remained unchanged.

PMID:
9341741
DOI:
10.1006/cimm.1997.1182
[Indexed for MEDLINE]
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