TY - JOUR
T1 - Cadherin-mediated cellular signaling
AU - Wheelock, Margaret J.
AU - Johnson, Keith R.
N1 - Funding Information:
The authors thank Dr. Karen Knudsen, Lankenau Institute for Medical Research and members of the Wheelock/Johnson laboratory for critically reviewing this manuscript. The Wheelock/Johnson laboratory is supported by grants GM51188 and DE12308 from the National Institutes of Health.
PY - 2003/10
Y1 - 2003/10
N2 - Recent cadherin studies focusing on cellular signaling have shown that several pathways are activated by cadherin-mediated cell-cell contact. Cadherin-mediated contacts activate Rho family GTPases, regulate the availability of β-catenin to participate in Wnt signaling, and function in receptor tyrosine kinase signaling. Although different classical cadherins bind to the same cytosolic proteins via their cytoplasmic tails, one message that is clear from the recent literature is that downstream signals emanating from cadherin-mediated contacts are both cadherin-specific and cell-context-specific.
AB - Recent cadherin studies focusing on cellular signaling have shown that several pathways are activated by cadherin-mediated cell-cell contact. Cadherin-mediated contacts activate Rho family GTPases, regulate the availability of β-catenin to participate in Wnt signaling, and function in receptor tyrosine kinase signaling. Although different classical cadherins bind to the same cytosolic proteins via their cytoplasmic tails, one message that is clear from the recent literature is that downstream signals emanating from cadherin-mediated contacts are both cadherin-specific and cell-context-specific.
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U2 - 10.1016/S0955-0674(03)00101-7
DO - 10.1016/S0955-0674(03)00101-7
M3 - Review article
C2 - 14519384
AN - SCOPUS:0141533082
SN - 0955-0674
VL - 15
SP - 509
EP - 514
JO - Current Opinion in Cell Biology
JF - Current Opinion in Cell Biology
IS - 5
ER -