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- W2117532336 abstract "As increase in collagen deposition is no longer taken as simply a consequence but, rather, an inducer of disease progression; therefore, the understanding of collagen signal transduction is fundamentally important. Cells contain at least two types of collagen receptors: integrins and discoidin domain receptors (DDRs). The integrin heterodimers α 1 β 1 , α 2 β 1 , α 10 β 1 , and α 11 β 1 are recognized as the non-tyrosine kinase collagen receptors. DDR1 and 2, the tyrosine kinase receptors of collagen, are specifically expressed in epithelium and mesenchyme, respectively. While integrin β 1 and DDR1 are both required for cell adhesion on collagen, their roles in epithelial cell differentiation during development and disease progression seem to counteract each other, with integrin β 1 favoring epithelium mesenchyme transition (EMT) and DDR1 inducing epithelial cell differentiation. The in vitro evidence shows that the integrin β 1 and DDR1 exert opposing actions in regulation of membrane stability of E-cadherin, which itself is a critical regulator of epithelial cell differentiation. Here, we review the functional roles of integrin β 1 and DDR1 in regulation of epithelial cell differentiation during development and disease progression, and explore the underlining mechanisms regarding to the regulation of membrane stability of E-cadherin." @default.
- W2117532336 created "2016-06-24" @default.
- W2117532336 creator A5058511539 @default.
- W2117532336 creator A5071217303 @default.
- W2117532336 creator A5078131390 @default.
- W2117532336 date "2012-12-15" @default.
- W2117532336 modified "2023-10-17" @default.
- W2117532336 title "A tale of two collagen receptors, integrin β<sub>1</sub>and discoidin domain receptor 1, in epithelial cell differentiation" @default.
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- W2117532336 doi "https://doi.org/10.1152/ajpcell.00253.2012" @default.
- W2117532336 hasPubMedId "https://pubmed.ncbi.nlm.nih.gov/23015544" @default.
- W2117532336 hasPublicationYear "2012" @default.
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