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PMID: 19221195 Published · ppublish English Journal Article Research Support, N.I.H., Intramural

One-dimensional topography underlies three-dimensional fibrillar cell migration.

The Journal of cell biology ·Vol. 184 ·No. 4 ·2009-02-23 ·Pages 481-90

Doyle AD, Wang FW, Matsumoto K, Yamada KM

Abstract

Current concepts of cell migration were established in regular two-dimensional (2D) cell culture, but the roles of topography are poorly understood for cells migrating in an oriented 3D fibrillar extracellular matrix (ECM). We use a novel micropatterning technique termed microphotopatterning (microPP) to identify functions for 1D fibrillar patterns in 3D cell migration. In striking contrast to 2D, cell migration in both 1D and 3D is rapid, uniaxial, independent of ECM ligand density, and dependent on myosin II contractility and microtubules (MTs). 1D and 3D migration are also characterized by an anterior MT bundle with a posterior centrosome. We propose that cells migrate rapidly through 3D fibrillar matrices by a 1D migratory mechanism not mimicked by 2D matrices.

MeSH Terms
Animals Cell Culture Techniques Cell Movement Extracellular Matrix/metabolism Fibroblasts/metabolism Mice Myosins/metabolism NIH 3T3 Cells
Chemicals
Myosins
Authors & Affiliations
4 authors, click to expand affiliations / ORCID
Doyle Andrew D
Laboratory of Cell and Developmental Biology, National Institute of Dental and Craniofacial Research, National Institutes of Health, Bethesda, MD 20892, USA. adoyle@mail.nih.gov
Wang Francis W
Matsumoto Kazue
Yamada Kenneth M
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Article Info
Journal
The Journal of cell biology
Abbr.
J Cell Biol
ISSN
1540-8140
Published
2009-02-23
Epub
2009-00-16
Pages
481-90
Language
English
Region
United States
NLM ID
0375356
PMCID
PMC2654121
Subset
IM
Grants
Intramural NIH HHS · United States
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