
Integrin-mediated cell adhesion is important for development, immune responses, hemostasis and wound healing. Integrins also function as signal transducing receptors that can control intracellular pathways that regulate cell survival, proliferation, and cell fate. Conversely, cells can modulate the affinity of integrins for their ligands a process operationally defined as integrin activation. Analysis of activation of integrins has now provided a detailed molecular understanding of this unique form of "inside-out" signal transduction and revealed new paradigms of how transmembrane domains (TMD) can transmit long range allosteric changes in transmembrane proteins. Here, we will review how talin and mediates integrin activation and how the integrin TMD can transmit these inside out signals.
Talin, Protein Structure, Biochemistry & Molecular Biology, Integrins, 1.1 Normal biological development and functioning, 610, Integrin, 612, Signal transduction, Transmembrane domain, Allosteric Regulation, Underpinning research, Cell Adhesion, Humans, Inflammatory and immune system, Cell adhesion, Biological Sciences, Invited Mini Review, Protein Structure, Tertiary, Biochemistry and cell biology, Biochemistry and Cell Biology, Nanodisc, Tertiary, Protein Binding
Talin, Protein Structure, Biochemistry & Molecular Biology, Integrins, 1.1 Normal biological development and functioning, 610, Integrin, 612, Signal transduction, Transmembrane domain, Allosteric Regulation, Underpinning research, Cell Adhesion, Humans, Inflammatory and immune system, Cell adhesion, Biological Sciences, Invited Mini Review, Protein Structure, Tertiary, Biochemistry and cell biology, Biochemistry and Cell Biology, Nanodisc, Tertiary, Protein Binding
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