Journal
CYTOSKELETON
Volume 72, Issue 5, Pages 235-245Publisher
WILEY-BLACKWELL
DOI: 10.1002/cm.21223
Keywords
focal adhesion; structured illumination microscopy; paxillin; mechanobiology; cytoskeleton; cell mechanics
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Funding
- Israel Science Foundation [956/10]
- Mechanobiology Institute (MBI)
- Laboratoire International Associe Cell Adhesion France-Singapour (CAFS)
- Agence Nationale de la Recherche [ICEBERG-ANR-10-BINF-06-01]
- Who am I? Laboratory of Excellence [ANR-11-LABX-0071, ANR-11-IDEX-0005-01]
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The ability to mechanically interact with the extracellular matrix is a fundamental feature of adherent eukaryotic cells. Cell-matrix adhesion in many cell types is mediated by protein complexes called focal adhesions (FAs). Recent progress in super resolution microscopy revealed FAs possess an internal organization, yet such methods do not enable observation of the formation and dynamics of their internal structure in living cells. Here, we combine structured illumination microscopy (SIM) with total internal reflection fluorescence microscopy (TIRF) to show that the proteins inside FA patches are distributed along elongated subunits, typically 300 +/- 100nm wide, separated by 400 +/- 100nm, and individually connected to actin cables. We further show that the formation and dynamics of these linear subunits are intimately linked to radial actin fiber formation and actomyosin contractility. We found FA growth to be the result of nucleation of new linear subunits and their coordinated elongation. Taken together, this study reveals that the basic units of mature focal adhesion are 300-nm-wide elongated, dynamic structures. We anticipate this ultrastructure to be relevant to investigation of the function of FAs and their behavior in response to mechanical stress. (c) 2015 Wiley Periodicals, Inc.
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