Integrin α6β4 and TRPV1 channel coordinately regulate directional keratinocyte migration

• Published in: Biochemical and biophysical research communications Vol. 458; no. 1; pp. 161 - 167
• Main Authors: Miyazaki, Ayako, Ohkubo, Tsuyako, Hatta, Mitsutoki, Ishikawa, Hiroyuki, Yamazaki, Jun
• Format: Journal Article
• Language: English
• Published: United States Elsevier Inc 27-02-2015
• Subjects: Animals; Calcium - metabolism; Calcium signal; Capsaicin - pharmacology; Cell migration; Cell Movement - drug effects; Cells, Cultured; Cobalt - metabolism; Epidermal Growth Factor - metabolism; Epidermal Growth Factor - pharmacology; Gene Silencing; Integrin alpha6beta4 - genetics; Integrin alpha6beta4 - metabolism; Integrin beta4; Keratinocytes - cytology; Keratinocytes - drug effects; Keratinocytes - metabolism; Mice; TRPV Cation Channels - genetics; TRPV Cation Channels - metabolism; TRPV1 channels; Up-Regulation; Wound Healing; Integrin beta4; Calcium signal; TRPV1 channels; Cell migration
• ISSN: 0006-291X; 1090-2104
• DOI: 10.1016/j.bbrc.2015.01.086

The directional migration of epithelial cells is crucial for wound healing. Among integrins, a family of cell adhesion receptors, integrin β4 has been assumed to be a promigratory factor, in addition to its role in stable adhesion. In turn, Ca2+ signaling is also a key coordinator of migration. Keratinocytes reportedly express transient receptor potential vanilloid channels (TRPV1); however, the function of these channels as a regulator of intracellular Ca2+ level in cell migration has remained uncharacterized. In the present study, we investigated the role of TRPV1 in directional migration related to integrin β4 using a scratch wound assay on a confluent monolayer sheet of murine keratinocytes (Pam212 cells). Double immunofluorescence staining revealed the de novo expression of integrin β4 and TRPV1 in migrating cells at the wound edge in response to scratch wounding, and both expression levels were almost matched. Epidermal growth factor (EGF) not only promoted keratinocyte migration, but also caused the further up-regulation of both integrin β4 and TRPV1. In addition, the knockdown of the integrin β4 or TRPV1 gene significantly impeded wound closure. The TRPV1 agonist capsaicin significantly promoted migration, while a selective TRPV1 antagonist inhibited it. The gene knockdown of TRPV1 inhibited the expression of the integrin β4 gene and that of β4 protein in migrating cells. These findings suggest that TRPV1 may stimulate directional migration directly by eliciting a Ca2+ signal or indirectly via integrin β4 expression.
•Role of TRPV1 in directional migration related to integrin β4 was investigated.•Both integrin β4 and TRPV1 contribute to keratinocyte migration.•The coincident up-regulation of integrin β4 and TRPV1 in migrating cells was observed.•The endogenous activation of TRPV1 accompanying Ca2+ influx occurs during migration.•The promigratory ability of TRPV1 partly reflects the promotion of β4 expression.