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p38 mitogen-activated protein kinase up-regulates NF-kappaB transcriptional activation through RelA phosphorylation during stretch-induced myogenesis.

Abstract：

:p38 MAPK and nuclear factor-B (NF-B) signaling pathways play an indispensable role in the control of skeletal myogenesis. The specific contribution of these signaling pathways to the response of myoblast to the mechanical stimulation and the molecular mechanisms underlying this response remain unresolved. Using an established in vitro model, we now show that p38 MAP kinase activity regulates the transcriptional activation of NF-kappaB in response to mechanical stimulation of myoblasts. Furthermore, SB203580 blocked stretch-induced NF-kappaB activation during myogenesis, not through down-regulation of degradation of IkappaB-alpha, and consequent translocation of the p65 subunit of NF-kappaB to the nucleus. It is likely that stretch-induced NF-kappaB activation by phosphorylation of p65 NF-kappaB. Moreover, depletion of p38alpha using siRNA significantly reduces stretch-induced phosphorylation of RelA and NF-kappaB activity. These results provides the first evidence of a cross-talk between p38 MAPK and NF-kappaB signaling pathways during stretch-induced myogenesis, with phosphorylation of RelA being one of the effectors of this promyogenic mechanism. The alpha isoform of p38MAP kinase regulates the transcriptional activation of NF-kappaB following stimulation with cyclic stretch.

journal_name

Biochem Biophys Res Commun

journal_title

Biochemical and biophysical research communications

authors

Ji G,Liu D,Liu J,Gao H,Yuan X,Shen G

doi

10.1016/j.bbrc.2009.11.095

subject

Has Abstract

pub_date

2010-01-01 00:00:00

pages

547-51

issue

1

eissn

0006-291X

issn

1090-2104

pii

S0006-291X(09)02272-4

journal_volume

391

pub_type

杂志文章

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