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

被引:102
作者
Kim, Areum
Lakshman, Neema
Petroll, W. Matthew
机构
[1] Univ Texas, Dept Ophthalmol, SW Med Ctr, Dallas, TX 75390 USA
[2] Univ Texas, Grad Program Biomed Engn, SW Med Ctr, Dallas, TX 75390 USA
关键词
collagen matrices; Rho kinase; corneal fibroblasts; cell mechanics; confocal microscopy; cytoskeleton; actin; myosin; Fourier transform;
D O I
10.1016/j.yexcr.2006.08.009
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
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.
引用
收藏
页码:3683 / 3692
页数:10
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