| First Author | Zhang YM | Year | 2015 |
| Journal | J Invest Dermatol | Volume | 135 |
| Issue | 1 | Pages | 181-191 |
| PubMed ID | 25078664 | Mgi Jnum | J:216191 |
| Mgi Id | MGI:5607847 | Doi | 10.1038/jid.2014.326 |
| Citation | Zhang YM, et al. (2015) Requirement of Galphai1/3-Gab1 Signaling Complex for Keratinocyte Growth Factor-Induced PI3K-AKT-mTORC1 Activation. J Invest Dermatol 135(1):181-91 |
| abstractText | Keratinocyte growth factor (KGF), also termed as fibroblast growth factor-7, promotes proliferation, migration, and adhesion of skin keratinocytes via binding to keratinocyte growth factor receptor (KGFR) and subsequent activation of downstream signaling including the PI3K-AKT-mTORC1 pathway. Here, we found that the alpha-subunits of the G proteins (Galphai1/3) and growth factor receptor binding 2-associated binding protein 1 (Gab1) are required for this activation process. With KGF stimulation, Galphai1/3 formed a complex with KGFR and was required for subsequent Gab1 recruitment, phosphorylation, and following PI3K-p85 activation. In addition, Galphai1/3 short hairpin RNA knockdown largely inhibited KGF-induced cell proliferation, migration, and the accumulation of cyclin D1/fibronectin in cultured skin keratinocytes. Furthermore, we observed increased expression of Galphai1/3 in wounded human skin and keloid skin tissues, suggesting the possible involvement of Galphai1/3 in wound healing and keloid formation. Overall, we suggest that Galphai1/3 proteins lie downstream of KGFR, but upstream of Gab1-mediated activation of PI3K-AKT-mTORC1 signaling, thus revealing a role for Galphai proteins in mediating KGFR signaling, cell migration, and possible wound healing. |
