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p38α and p38δ MAPK are key regulators of p21 Cip1 gene expression in human keratinocytes
Author(s) -
Saha Kamalika,
Eckert Richard L.
Publication year - 2013
Publication title -
the faseb journal
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.709
H-Index - 277
eISSN - 1530-6860
pISSN - 0892-6638
DOI - 10.1096/fasebj.27.1_supplement.lb110
Subject(s) - p38 mitogen activated protein kinases , microbiology and biotechnology , effector , kinase , protein kinase c , biology , regulation of gene expression , mapk/erk pathway , keratinocyte , gene expression , gene , cell culture , biochemistry , genetics
PKCδ increases keratinocyte differentiation via a mechanism that involves activation of p38δ MAPK. We recently showed that PKCδ also suppresses cell proliferation by increasing expression of the p21 Cip1 cyclin‐dependent kinase inhibitor. However, the downstream effectors that mediate this PKCδ‐dependent regulation are not known. Our present studies suggest that PKCδ activates p38δ which regulates p21 Cip1 promoter activity, as exogenously expressed p38δ increases p21 Cip1 mRNA and protein level in human keratinocytes. Treatment with SB202190, a p38α/β inhibitor, or dominant negative p38α, leads to a decrease in PKCδ‐dependent p21 Cip1 promoter activity, implicating p38α as a second mediator of this regulation. p21 Cip1 promoter truncation experiments indicate that p38δ increases the activity via a putative p53 response element. This suggests that p38α and δ may act in conjunction with or through p53 to regulate p21 Cip1 gene expression. In addition, we show that p38α and p38δ overexpression increases p53 promoter activity, suggesting that p38α and δ regulate p53 gene expression. We propose that PKCδ activates p38α and p38δ which in turn activates p53 to increase p21 Cip1 expression leading to cessation of keratinocyte proliferation.