TY - JOUR
T1 - Regulation of cell-cell adhesion of MDCK cells by Cdc42 and Rac1 small GTPases
AU - Kuroda, Shinya
AU - Fukata, Masaki
AU - Fujii, Katsuhiko
AU - Nakamura, Tomoko
AU - Izawa, Ichiro
AU - Kaibuchi, Kozo
N1 - Funding Information:
We thank Drs. A. Nagafuchi and Sh. Tsukita (Kyoto University, Japan) and Dr. M. Takeichi (Kyoto University, Japan) for providing the anti-E-cadherin antibody and helpful discussion. This study was supported by grants-in-aid for Scienti®c Research and for Cancer Research from the Ministry of Education, Science and Culture, Japan (1996), and by grants from the Mitsubishi Foundation and Kirin Brewery Company Limited.
PY - 1997/11/17
Y1 - 1997/11/17
N2 - Rac1, a member of the Rho small GTPases family, has recently been shown to be involved in the regulation of cell-cell adhesion mediated by cadherin. Here we showed that Cdc42, another member of Rho family, accumulated at cell-cell contact sites. Microinjection of Rho GDI, a negative regulator of the Rho family members, into Madin-Darby canine kidney (MDCK) cells resulted in perturbation of epithelial cell morphology and of cell cell and cell-substratum adhesions, and comicroinjection of dominant active Cdc42 or Rac1 reversed the action of Rho GDI, suggesting that the active form of Cdc42 or Rac1 is required for maintaining the cell-cell and cell-substratum adhesions. These observations suggest that Cdc42, in addition to Rac1, can regulate the cell-cell adhesion.
AB - Rac1, a member of the Rho small GTPases family, has recently been shown to be involved in the regulation of cell-cell adhesion mediated by cadherin. Here we showed that Cdc42, another member of Rho family, accumulated at cell-cell contact sites. Microinjection of Rho GDI, a negative regulator of the Rho family members, into Madin-Darby canine kidney (MDCK) cells resulted in perturbation of epithelial cell morphology and of cell cell and cell-substratum adhesions, and comicroinjection of dominant active Cdc42 or Rac1 reversed the action of Rho GDI, suggesting that the active form of Cdc42 or Rac1 is required for maintaining the cell-cell and cell-substratum adhesions. These observations suggest that Cdc42, in addition to Rac1, can regulate the cell-cell adhesion.
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U2 - 10.1006/bbrc.1997.7675
DO - 10.1006/bbrc.1997.7675
M3 - Article
C2 - 9388496
AN - SCOPUS:0031576553
SN - 0006-291X
VL - 240
SP - 430
EP - 435
JO - Biochemical and Biophysical Research Communications
JF - Biochemical and Biophysical Research Communications
IS - 2
ER -