Distinct signaling mechanisms regulate migration in unconfined versus confined spaces

Wei Chien Hung, Shih Hsun Chen, Colin D. Paul, Kimberly M. Stroka, Ying Chun Lo, Joy T. Yang, Konstantinos Konstantopoulos

Research output: Contribution to journalArticle

Abstract

Using a microchannel assay, we demonstrate that cells adopt distinct signaling strategies to modulate cell migration in different physical microenvironments. We studied α4β1 integrin-mediated signaling, which regulates cell migration pertinent to embryonic development, leukocyte trafficking, and melanoma invasion. We show that α4β1 integrin promotes cell migration through both unconfined and confined spaces. However, unlike unconfined (2D) migration, which depends on enhanced Rac1 activity achieved by preventing α4/paxillin binding, confined migration requires myosin II-driven contractility, which is increased when Rac1 is inhibited by α4/paxillin binding. This Rac1-myosin II cross talk mechanism also controls migration of fibroblast-like cells lacking α4β1 integrin, in which Rac1 and myosin II modulate unconfined and confined migration, respectively. We further demonstrate the distinct roles of myosin II isoforms, MIIA and MIIB, which are primarily required for confined and unconfined migration, respectively. This work provides a paradigm for the plasticity of cells migrating through different physical microenvironments.

Original languageEnglish (US)
Pages (from-to)807-824
Number of pages18
JournalJournal of Cell Biology
Volume202
Issue number5
DOIs
StatePublished - 2013

ASJC Scopus subject areas

  • Cell Biology

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