| First Author | Yonemura S | Year | 2004 |
| Journal | Exp Cell Res | Volume | 295 |
| Issue | 2 | Pages | 300-14 |
| PubMed ID | 15093731 | Mgi Jnum | J:89351 |
| Mgi Id | MGI:3039970 | Doi | 10.1016/j.yexcr.2004.01.005 |
| Citation | Yonemura S, et al. (2004) Rho localization in cells and tissues. Exp Cell Res 295(2):300-14 |
| abstractText | Rho family small GTPases regulate cytoskeletal organization. Although their spatiotemporal activities appear to be important for cellular morphogenesis, there has been little characterization of the localization of Rho family GTPases in cells and tissues. Here we show precise localization of Rho subfamily proteins in mammalian cultured cells and tissues through evaluation of anti-Rho antibodies and fixation protocols. Although Rho is not a structural protein but functions as a switching molecule, it often localizes at several distinct domains or structures of cells. In cultured epithelial cells, Rho was highly accumulated at lateral membranes. However, in fibroblastic cells, Rho appeared to be distributed evenly in the cytoplasm. Rho concentration at the cleavage furrow at cytokinesis was generally observed. In A431 cells, Rho translocation from the cytoplasm to elongating microvilli at the apical membrane within 30 s after EGF stimulation was clearly demonstrated. Also, Myc- or GFP-tagged RhoA did not always reflect the localization of endogenous Rho, indicating a drawback of protein-tagging methods for localization research. In mouse tissues, Rho localization differed depending on cell type, probably reflecting the functional differences of each cell type. |
