Lysophosphatidic acid enhances collagen deposition and matrix thickening in engineered tissue

被引:21
作者
Chabaud, Stephane [1 ]
Marcoux, Thomas-Louis [1 ]
Deschenes-Rompre, Marie-Pier [1 ]
Rousseau, Alexandre [1 ]
Morissette, Amelie [1 ]
Bouhout, Sara [1 ]
Bernard, Genevieve [1 ]
Bolduc, Stephane [1 ]
机构
[1] Univ Laval, Fac Med, Genie Tissulaire & Regenerat LOEX Ctr Rech FRQS, Dept Chirurg,Ctr LOEX,Ctr Hosp Affilie Univ Quebe, Quebec City, PQ G1K 7P4, Canada
基金
加拿大健康研究院;
关键词
matrix; lysophosphatidic acid; L-arginine; collagen; EXTRACELLULAR-MATRIX; MOLECULAR-CLONING; FIBROSIS; MODEL; MYOFIBROBLAST; CONTRACTION; EQUIVALENT; RECEPTOR;
D O I
10.1002/term.1711
中图分类号
Q813 [细胞工程];
学科分类号
摘要
The time needed to produce engineered tissue is critical. A self-assembly approach provided excellent results regarding biological functions and cell differentiation because it closely respected the microenvironment of cells. Nevertheless, the technique was time consuming for producing tissue equivalents with enough extracellular matrix to allow manipulations. Unlike L-arginine supplementation that only increased accumulation of collagen in cell culture supernatant in our model, addition of lysophosphatidic acid, a natural bioactive lipid, did not modify the amount of accumulated collagen in the cell culture supernatant; however, it enhanced the matrix deposition rate without inducing fibroblast hyperproliferation and tissue fibrosis. Copyright (C) 2013 John Wiley & Sons, Ltd.
引用
收藏
页码:E65 / E75
页数:11
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