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G Protein betagamma subunits augment UVB-induced apoptosis by stimulating the release of soluble heparin-binding epidermal growth factor from human keratinocytes.

Authors
Seo, M; Lee, MJ; Heo, JH; Lee, YI; Kim, Y; Kim, SY; Lee, ES; Juhnn, YS
Citation
The Journal of biological chemistry, 282(34):24720-24730, 2007
Journal Title
The Journal of biological chemistry
ISSN
0021-92581083-351X
Abstract
UV radiation induces various cellular responses by regulating the activity of many UV-responsive enzymes, including MAPKs. The betagamma subunit of the heterotrimeric GTP-binding protein (Gbetagamma) was found to mediate UV-induced p38 activation via epidermal growth factor receptor (EGFR). However, it is not known how Gbetagamma mediates the UVB-induced activation of EGFR, and thus we undertook this study to elucidate the mechanism. Treatment of HaCaT-immortalized human keratinocytes with conditioned medium obtained from UVB-irradiated cells induced the phosphorylations of EGFR, p38, and ERK but not that of JNK. Blockade of heparin-binding EGF-like growth factor (HB-EGF) by neutralizing antibody or CRM197 toxin inhibited the UVB-induced activations of EGFR, p38, and ERK in normal human epidermal keratinocytes and in HaCaT cells. Treatment with HB-EGF also activated EGFR, p38, and ERK. UVB radiation stimulated the processing of pro-HB-EGF and increased the secretion of soluble HB-EGF in medium, which was quantified by immunoblotting and protein staining. In addition, treatment with CRM179 toxin blocked UV-induced apoptosis, but HB-EGF augmented this apoptosis. Moreover, UVB-induced apoptosis was reduced by inhibiting EGFR or p38. The overexpression of Gbeta(1)gamma(2) increased EGFR-activating activity and soluble HB-EGF content in conditioned medium, but the sequestration of Gbetagamma by the carboxyl terminus of G protein-coupled receptor kinase 2 (GRK2ct) produced the opposite effect. The activation of Src increased UVB-induced, Gbetagamma-mediated HB-EGF secretion, but the inhibition of Src blocked that. Overexpression of Gbetagamma increased UVB-induced apoptosis, and the overexpression of GRK2ct decreased this apoptosis. We conclude that Gbetagamma mediates UVB-induced human keratinocyte apoptosis by augmenting the ectodomain shedding of HB-EGF, which sequentially activates EGFR and p38.
MeSH terms
Apoptosis*Cell Line, TumorCulture Media, Conditioned/pharmacologyDose-Response Relationship, DrugEpidermal Growth Factor/metabolism*GTP-Binding Protein beta Subunits/chemistryGTP-Binding Protein beta Subunits/physiology*GTP-Binding Protein gamma Subunits/chemistryGTP-Binding Protein gamma Subunits/physiology*HumansIntercellular Signaling Peptides and ProteinsKeratinocytes/metabolism*Keratinocytes/pathologyModels, BiologicalPhosphorylationProtein BindingReceptor, Epidermal Growth Factor/metabolismUltraviolet Rays*p38 Mitogen-Activated Protein Kinases/metabolismsrc-Family Kinases/metabolism
DOI
10.1074/jbc.M702343200
PMID
17548351
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Journal Papers > School of Medicine / Graduate School of Medicine > Dermatology
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