Deconstructing fibrosis research: do pro-fibrotic signals point the way for chronic dermal wound regeneration?

被引:34
作者
Elliott, Christopher G. [1 ]
Hamilton, Douglas W. [1 ,2 ,3 ]
机构
[1] Univ Western Ontario, Dept Anat & Cell Biol, London, ON N6A 5C1, Canada
[2] Univ Western Ontario, Div Oral Biol, Schulich Sch Med & Dent, London, ON N6A 5C1, Canada
[3] Univ Western Ontario, Schulich Sch Med & Dent, London, ON N6A 5C1, Canada
关键词
Chronic dermal wounds; Fibrosis; Matricellular proteins; Periostin; Transforming growth factor beta; Dermal fibroblast;
D O I
10.1007/s12079-011-0131-5
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Chronic wounds are characterized by inadequate matrix synthesis, no re-epithelialization, infection and ultimately no wound resolution. In contrast, fibrosis is characterized by overproduction of matrix and excess matrix contraction. As research in the fields of chronic wounds and fibrosis surges forward, important parallels can now be drawn between the dysfunctions in fibrotic diseases and the needs of chronic wounds. These parallels exist at both the macroscopic level and at the molecular level. Thus in finding the individual factors responsible for the progression of fibrotic diseases, we may identify new therapeutic targets for the resolution of chronic wounds. The aim of this review is to discuss how recent advances in fibrosis research have found a home in the treatment of chronic wounds and to highlight the benefits that can be obtained for chronic wound treatments by employing a translational approach to molecules identified in fibrosis research.
引用
收藏
页码:301 / 315
页数:15
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