Translocation of protein kinase C epsilon and protein kinase C delta to membrane is required for ultraviolet B-induced activation of mitogen-activated protein kinases and apoptosis

Citation
Ny. Chen et al., Translocation of protein kinase C epsilon and protein kinase C delta to membrane is required for ultraviolet B-induced activation of mitogen-activated protein kinases and apoptosis, J BIOL CHEM, 274(22), 1999, pp. 15389-15394
Citations number
49
Categorie Soggetti
Biochemistry & Biophysics
Journal title
JOURNAL OF BIOLOGICAL CHEMISTRY
ISSN journal
00219258 → ACNP
Volume
274
Issue
22
Year of publication
1999
Pages
15389 - 15394
Database
ISI
SICI code
0021-9258(19990528)274:22<15389:TOPKCE>2.0.ZU;2-K
Abstract
UV-induced signal transduction may be involved in tumor promotion and induc tion of apoptosis, The role of protein kinase C (PKC) in UVB-induced signal transduction is not well understood. This study showed that UVB markedly i nduced translocation of membrane-associated PKC epsilon and PKC delta, but not PKC alpha, from cytosol to membrane. Dominant negative mutant (DNM) PKC epsilon or PKC delta inhibited UVB-induced translocation of PKC epsilon an d PKC delta, respectively, UVB-induced activation of extracellular signal-r egulated protein kinases (Erks) and c-Jun NH2-terminal kinases (JNKs) was s trongly inhibited by DNM PKC epsilon and PKC delta, whereas the DNM of PKC alpha was less effective on the UVB-induced phosphorylation of Erks and JNK s, Among the PKC inhibitors used only rottlerin, a selective inhibitor of P KC delta, markedly inhibited the UVB-induced activation of Erks and JNKs, b ut not p38 kinases, Safingol, a selective inhibitor for PKC alpha, did not show any inhibitory effect on UVB-induced mitogen-activated protein kinase activation. GF109203X is a stronger inhibitor of classical PKC than novel P KC, Lower concentrations of GF109203X (<10 mu M) had no effect on UVB-induc ed activation of Erks or JNKs, However, at higher concentrations (over 20 m u M), GF109203X inhibited UVB-induced activation of JNKs, Erks, and even p3 8 kinases. Meanwhile, rottlerin and GF109203X markedly inhibited UVB-induce d apoptosis of JB6 cells, whereas safingol had little inhibitory effect. DN M-Erk2 cells and PD98059, a selective inhibitor for mitogen-activated prote in kinase/extracellular signal-regulated kinase 1 that directly activates E rks, inhibited UVB-induced apoptosis. DNM-JNK1 cells also blocked UVB-induc ed apoptosis, whereas SB202190, a specific inhibitor for p38 kinases, did n ot produce the inhibitory effect. These data demonstrate that PKC delta and PKC epsilon, but not PKC alpha, mediate UVB-induced signal transduction an d apoptosis in JB6 cells through activation of Erks and JNKs.