4.6 Article

Quantitative assessment of local collagen matrix remodeling in 3-D Culture: The role of Rho kinase

Journal

EXPERIMENTAL CELL RESEARCH
Volume 312, Issue 18, Pages 3683-3692

Publisher

ELSEVIER INC
DOI: 10.1016/j.yexcr.2006.08.009

Keywords

collagen matrices; Rho kinase; corneal fibroblasts; cell mechanics; confocal microscopy; cytoskeleton; actin; myosin; Fourier transform

Funding

  1. NEI NIH HHS [R01 EY13322, R24 EY016664, R01 EY013322, R24 EY16664] Funding Source: Medline

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The purpose of this study was to quantitatively assess the role of Rho kinase in modulating the pattern and amount of local cell-induced collagen matrix remodeling. Human corneal fibroblasts were plated inside 100-mu m thick fibrillar collagen matrices and cultured for 24 h in media with or without the Rho kinase inhibitor Y-27632. Cells were then fixed and stained with phalloidin. Fluorescent (for f-actin) and reflected light (for collagen fibrils) 3-D optical section images were acquired using laser confocal microscopy. Fourier transform analysis was used to assess collagen fibril alignment, and 3-D cell morphology and local collagen density were measured using MetaMorph. Culture in serum-containing media induced significant global matrix contraction, which was inhibited by blocking Rho kinase (p < 0.001). Fibroblasts generally had a bipolar morphology and intracellular stress fibers. Collagen fibrils were compacted and aligned parallel to stress fibers and pseudopodia. When Rho kinase was inhibited, cells had a more cortical f-actin distribution and dendritic morphology. Both local collagen fibril density and alignment were significantly reduced (p < 0.01). Overall, the data suggests that Rho kinase-dependent contractile force generation leads to co-alignment of cells and collagen fibrils along the plane of greatest resistance, and that this process contributes to global matrix contraction. (c) 2006 Elsevier Inc. All rights reserved.

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