| First Author | Yamada S | Year | 2023 |
| Journal | Biochem Biophys Res Commun | Volume | 643 |
| Pages | 55-60 | PubMed ID | 36586159 |
| Mgi Jnum | J:333156 | Mgi Id | MGI:7432085 |
| Doi | 10.1016/j.bbrc.2022.12.068 | Citation | Yamada S, et al. (2023) Inka2 expression in smooth muscle cells and its involvement in cell migration. Biochem Biophys Res Commun 643:55-60 |
| abstractText | The cell motility of smooth muscle cells (SMCs) is essential for vascular and internal organ development and tissue regeneration in response to damage. Cell migration requires dynamic changes in the actin-cytoskeleton via the p-21 activated kinase (Pak)-Cofilin signaling cascade, which is the central axis of the actin filaments. We previously identified that the Inka2 gene was preferentially expressed in the central nervous system (CNS) and revealed that Inka2 directly binds Pak4 to suppress its kinase activity, thereby regulating actin de-polymerization in dendritic spine formation of the forebrain neurons. However, its physiological significance outside the CNS remains unclear. Here we determined the Inka2 expression profile in various organs using in situ hybridization analysis and lacZ staining on Inka2(flox/+) mice. Robust Inka2 expression was consistently detected in the SMCs of many peripheral organs, including the arteries, esophagus, stomach, intestine, and bladder. The scratch assay was used on primary cultured SMCs and revealed that Inka2(-/-) SMC exhibits accelerated cell migration ability without a change in the cell proliferation rate. Inka2(-/-) SMCs displayed Cofilin activation/phosphorylation, a downstream molecule of Pak4 signal cascade. These results suggest that Inka2 regulates SMC motility through modulating actin reorganization as the endogenous inhibitor of Pak4. |
