Spatial-temporal reorganization of activated integrins

Cheng Han Yu, Weiwei Luo, Michael P. Sheetz

Research output: Contribution to journalReview articlepeer-review

12 Scopus citations


Integrin receptors play important roles in cell adhesion and tumor metastasis. The coupling of mechanical sensing and biochemical ligation is known to collectively regulate the activation of integrin receptors. Recently, oligomerization of activated integrins has been considered as the primordial signature of cytoskeletal remodeling and the initiation of various downstream signals, such as focal and fibrillar adhesions. However, spatio-temporal reorganization of activated integrins and associated proteins remains poorly understood. Here, we summarized the recent discovery of sequential biophysical events of integrin activation during early adhesion formation. Using the cyclic Arg-Gly-Asp (RGD) peptide as a mobile ligand on supported lipid membranes, a series of previously unreported events were observed following integrin avb3 clustering and cell spreading, including a long-range lateral translocation of the integrin clusters. With initial clustering, localized actin polymerization occurred in a Src family kinase dependent manner. Clustering of liganded integrins recruits various adaptor proteins and serves as a reaction core for mechanobiological activities. In addition, there are future possibilities to investigate the role of other synergetic interactions with the activated integrin receptors.

Original languageEnglish (US)
Pages (from-to)280-284
Number of pages5
JournalCell Adhesion and Migration
Issue number3
StatePublished - 2012
Externally publishedYes


  • Actin polymerization
  • Integrin
  • RGD peptide
  • Src family kinase
  • Supported lipid membrane
  • Synergy receptor
  • Tumor metastasis

ASJC Scopus subject areas

  • Cellular and Molecular Neuroscience
  • Cell Biology


Dive into the research topics of 'Spatial-temporal reorganization of activated integrins'. Together they form a unique fingerprint.

Cite this