RRC ID 87175
著者 Yamada S, Tokunaga A, Sakakibara SI.
タイトル Inka2 expression in smooth muscle cells and its involvement in cell migration.
ジャーナル Biochem Biophys Res Commun
Abstract 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 Inka2flox/+ 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.
巻・号 643
ページ 55-60
公開日 2023-2-5
DOI 10.1016/j.bbrc.2022.12.068
PII S0006-291X(22)01738-7
PMID 36586159
MeSH Actin Cytoskeleton / metabolism Actin Depolymerizing Factors / metabolism Actins* / metabolism Adaptor Proteins, Signal Transducing Animals Cell Movement / physiology Cells, Cultured Mice Myocytes, Smooth Muscle* / metabolism
IF 2.985
リソース情報
実験動物マウス RBRC01828