Intermolecular transmembrane domain interactions activate integrin αIIbβ3

Feng Ye, Se Jong Kim, Chungho Kim

Research output: Contribution to journalArticle

4 Citations (Scopus)

Abstract

Integrins are the major cell adhesion molecules responsible for cell attachment to the extracellular matrix. The strength of integrin-mediated adhesion is controlled by the affinity of individual integrins (integrin activation) as well as by the number of integrins involved in such adhesion. The positive correlation between integrin activation and integrin clustering had been suggested previously, but several trials to induce integrin clustering by dimerization of the transmembrane domain or tail region of integrin α subunits failed to demonstrate any change in integrin activation. Here, using platelet integrin αIIbβ3 as a model system, we showed that there is intermolecular lateral interaction between integrins through the transmembrane domains, and this interaction can enhance the affinity state of integrins. In addition, when integrin clustering was induced through heteromeric lateral interactions using bimolecular fluorescence complementation, we could observe a significant increase in the number of active integrin molecules. Because the possibility of intermolecular interaction would be increased by a higher local concentration of integrins, we propose that integrin clustering can shift the equilibrium in favor of integrin activation

Original languageEnglish
Pages (from-to)18507-18513
Number of pages7
JournalJournal of Biological Chemistry
Volume289
Issue number26
DOIs
Publication statusPublished - 2014 Jun 27

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Integrins
Cluster Analysis
Chemical activation
Adhesion
Dimerization
Cell Adhesion Molecules
Platelets
Extracellular Matrix

ASJC Scopus subject areas

  • Biochemistry
  • Cell Biology
  • Molecular Biology

Cite this

Intermolecular transmembrane domain interactions activate integrin αIIbβ3. / Ye, Feng; Kim, Se Jong; Kim, Chungho.

In: Journal of Biological Chemistry, Vol. 289, No. 26, 27.06.2014, p. 18507-18513.

Research output: Contribution to journalArticle

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