TY - JOUR
T1 - A regulatory role for p38δ MAPK in keratinocyte differentiation
T2 - Evidence for p38δ-ERK1/2 complex formation
AU - Efimova, Tatiana
AU - Broome, Ann Marie
AU - Eckert, Richard L.
PY - 2003/9/5
Y1 - 2003/9/5
N2 - p38 MAPK isoforms are important in the regulation of a variety of cellular processes. Among the four described p38 isoforms, p38α, β, and δ are expressed in keratinocytes (Dashti, S. R., Efimova, T., and Eckert, R. L. (2001) J. Biol. Chem. 276, 8059-8063). However, very little is known about how individual p38 isoforms regulate keratinocyte function. In the present study, we use okadaic acid (OA) as a tool to study the role of p38 MAPKs as regulators of keratinocyte differentiation. We demonstrate that OA activates p38δ but not other p38 isoforms. p38δ activation is increased as early as 0.5 h after OA addition, and activity is maximal at 8 and 24 h. ERK1 and ERK2 activity are reduced on an identical time course. We show that p38δ forms a complex with ERK1/2, and overexpression of p38δ inhibits ERK1/2 activity without reducing ERK1/2 level. Thus, p38δ may directly suppress ERK1/2 activity. Additional studies show that p38δ is expressed in the epidermis, suggesting a role for p38δ in regulating differentiation. To evaluate its function, we show that increased p38δ activity is associated with increased levels of AP1 and CAATT enhancer binding protein factors, increased binding of these factors to the involucrin (hINV) promoter, and increased expression. Moreover, these responses are maintained in the presence of SB203580, an agent that inhibits p38α and β, further suggesting a central role for the p38δ isoform. Dominant-negative p38 also inhibits these responses. These unique observations suggest that p38δ is the major p38 isoform driving suprabasal hINV gene expression and that p38δ directly regulates ERK1/2 activity via formation of a p38δ-ERK1/2 complex.
AB - p38 MAPK isoforms are important in the regulation of a variety of cellular processes. Among the four described p38 isoforms, p38α, β, and δ are expressed in keratinocytes (Dashti, S. R., Efimova, T., and Eckert, R. L. (2001) J. Biol. Chem. 276, 8059-8063). However, very little is known about how individual p38 isoforms regulate keratinocyte function. In the present study, we use okadaic acid (OA) as a tool to study the role of p38 MAPKs as regulators of keratinocyte differentiation. We demonstrate that OA activates p38δ but not other p38 isoforms. p38δ activation is increased as early as 0.5 h after OA addition, and activity is maximal at 8 and 24 h. ERK1 and ERK2 activity are reduced on an identical time course. We show that p38δ forms a complex with ERK1/2, and overexpression of p38δ inhibits ERK1/2 activity without reducing ERK1/2 level. Thus, p38δ may directly suppress ERK1/2 activity. Additional studies show that p38δ is expressed in the epidermis, suggesting a role for p38δ in regulating differentiation. To evaluate its function, we show that increased p38δ activity is associated with increased levels of AP1 and CAATT enhancer binding protein factors, increased binding of these factors to the involucrin (hINV) promoter, and increased expression. Moreover, these responses are maintained in the presence of SB203580, an agent that inhibits p38α and β, further suggesting a central role for the p38δ isoform. Dominant-negative p38 also inhibits these responses. These unique observations suggest that p38δ is the major p38 isoform driving suprabasal hINV gene expression and that p38δ directly regulates ERK1/2 activity via formation of a p38δ-ERK1/2 complex.
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U2 - 10.1074/jbc.M302759200
DO - 10.1074/jbc.M302759200
M3 - Article
C2 - 12810719
AN - SCOPUS:0141557549
SN - 0021-9258
VL - 278
SP - 34277
EP - 34285
JO - Journal of Biological Chemistry
JF - Journal of Biological Chemistry
IS - 36
ER -