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PMID: 12714499 Published · ppublish English Journal Article Research Support, U.S. Gov't, P.H.S. Review

New insights into the structural basis of integrin activation.

Blood ·Vol. 102 ·No. 4 ·2003-08-15 ·Pages 1155-9

Xiong JP, Stehle T, Goodman SL, Arnaout MA

Abstract

Integrins are cell adhesion receptors that communicate biochemical and mechanical signals in a bidirectional manner across the plasma membrane and thus influence most cellular functions. Intracellular signals switch integrins into a ligand-competent state as a result of elicited conformational changes in the integrin ectodomain. Binding of extracellular ligands induces, in turn, structural changes that convey distinct signals to the cell interior. The structural basis of this bidirectional signaling has been the focus of intensive study for the past 3 decades. In this perspective, we develop a new hypothesis for integrin activation based on recent crystallographic, electron microscopic, and biochemical studies.

MeSH Terms
Binding Sites Dimerization Humans Integrins/chemistry,metabolism Ligands Models, Molecular Protein Binding Protein Conformation Protein Structure, Tertiary Signal Transduction
Chemicals
Integrins Ligands
Authors & Affiliations
4 authors, click to expand affiliations / ORCID
Xiong Jian-Ping
Renal Unit, Leukocyte Biology and Inflammation Program, Structural Biology Program, Massachusetts General Hospital, and Harvard Medical School, Charlestown, MA 02129, USA.
Stehle Thilo
Goodman Simon L
Arnaout M Amin
Article Info
Journal
Blood
Abbr.
Blood
ISSN
0006-4971
Published
2003-08-15
Epub
2003-00-24
Pages
1155-9
Language
English
Region
United States
NLM ID
7603509
Subset
IM
Grants
NIDDK NIH HHS · R01 DK048549 · United States
NHLBI NIH HHS · R01 HL070219 · United States
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