hide
Free keywords:
cardiomyocyte
collagen
extracellular matrix (ECM)
gene expression
p38 MAPK
transcription factor
activated protein-kinase
collagen gene-expression
messenger-rna
i
collagen
posttranscriptional regulation
cardiac fibroblasts
transgenic mice
p38
cells
binding
Biochemistry & Molecular Biology
Abstract:
p38 MAPKs (mitogen-activated protein kinases) play important roles in the regulation of cellular responses to environmental stress. Recently, this signalling pathway has also been implicated in the regulation of processes unrelated to stress, for example, in T lymphocytes and cardiomyocytes. In order to identify molecular targets responsible for the housekeeping functions of p38 MAPKs, we have analysed the differences in the transcriptomes of normally proliferating wild-type and p38 alpha knockout immortalized embryonic cardiomyocytes. Interestingly, many potential components of the myocardium extracellular matrix were found to be upregulated in the absence of p38 alpha. Further analysis of the microarray data identified TEF-1 (transcriptional enhancer factor-1), a known regulator of heart-specific gene expression, and C/EBP beta (CCAAT/enhancer-binding protein beta), as the two transcription factors the binding sites of which were most enriched in the promoters of p38 alpha-regulated genes. We have focused on the study of the extracellular matrix component COL1A1 (alpha 1 chain of type I collagen) and found evidence for the involvement of both TEF-1 and C/EBP beta in the p38 alpha-dependent inhibition of COL1A1 transcription. Our data therefore show that p38 MAPKs regulate TEF-1 and C/EBP beta transcriptional activity in the absence of environmental stress and suggests a role for p38a in the expression of extracellular matrix components that maintain organ architecture.
