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Fibroblast mechanics in 3D collagen matricesopen access

Authors
Rhee, SangmyungGrinnell, Frederick
Issue Date
Nov-2007
Publisher
ELSEVIER
Keywords
adhesion; migration; contraction; extracellular matrix; wound repair; tissue engineering; tensegrity; platelet-derived growth factor; lysophosphatidic acid
Citation
ADVANCED DRUG DELIVERY REVIEWS, v.59, no.13, pp 1299 - 1305
Pages
7
Journal Title
ADVANCED DRUG DELIVERY REVIEWS
Volume
59
Number
13
Start Page
1299
End Page
1305
URI
https://scholarworks.bwise.kr/cau/handle/2019.sw.cau/57711
DOI
10.1016/j.addr.2007.08.006
ISSN
0169-409X
1872-8294
Abstract
Connective tissues provide mechanical support and frameworks for the other tissues of the body. Type I collagen is the major protein component of ordinary connective tissue, and fibroblasts are the cell type primarily responsible for its biosynthesis and remodeling. Research on fibroblasts interacting with collagen matrices explores all four quadrants of cell mechanics: pro-migratory vs. pro-contractile growth factor environments on one axis; high tension vs. low tension cell-matrix interactions on the other. The dendritic fibroblast - probably equivalent to the resting tissue fibroblast - can be observed only in the low tension quadrant and generally has not been appreciated from research on cells incubated with planar culture surfaces. Fibroblasts in the low tension quadrant require micrombules for fori-nation of dendritic extensions, whereas fibroblasts in the high tension quadrant require micrombules for polarization but not for spreading. Ruffling of dendritic extensions rather than their overall protrusion or retraction provides the mechanism for remodeling of floating collagen matrices, and floating matrix remodeling likely reflects a model of tissue mechanical homeostasis. (C) 2007 Elsevier B.V. All rights reserved.
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Rhee, Sang Myung
자연과학대학 (생명과학과)
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