myofibroblast, a key cell in normal and pathological tissue repair

Myofibroblasts are characterized by their expression of α-smooth muscle actin, their enhanced contractility when compared to normal fibroblasts and their increased synthetic activity of extracellular matrix proteins. Myofibroblasts play an important role in normal tissue repair processes, particular...

Full description

Saved in:
Bibliographic Details
Published in:Cellular and molecular life sciences : CMLS Vol. 73; no. 6; pp. 1145 - 1157
Main Authors: Darby, Ian A, Zakuan, Noraina, Billet, Fabrice, Desmoulière, Alexis
Format: Journal Article
Language:English
Published: Cham Springer International Publishing 01.03.2016
Springer Nature B.V
Springer Verlag
Subjects:
ISSN:1420-682X, 1420-9071, 1420-9071
Online Access:Get full text
Tags: Add Tag
No Tags, Be the first to tag this record!
Description
Summary:Myofibroblasts are characterized by their expression of α-smooth muscle actin, their enhanced contractility when compared to normal fibroblasts and their increased synthetic activity of extracellular matrix proteins. Myofibroblasts play an important role in normal tissue repair processes, particularly in the skin where they were first described. During normal tissue repair, they appear transiently and are then lost via apoptosis. However, the chronic presence and continued activity of myofibroblasts characterize many fibrotic pathologies, in the skin and internal organs including the liver, kidney and lung. More recently, it has become clear that myofibroblasts also play a role in many types of cancer as stromal or cancer-associated myofibroblast. The fact that myofibroblasts are now known to be key players in many pathologies makes understanding their functions, origin and the regulation of their differentiation important to enable them to be regulated in normal physiology and targeted in fibrosis, scarring and cancer.
Bibliography:http://dx.doi.org/10.1007/s00018-015-2110-0
ObjectType-Article-1
SourceType-Scholarly Journals-1
ObjectType-Feature-2
content type line 14
ObjectType-Review-3
content type line 23
ISSN:1420-682X
1420-9071
1420-9071
DOI:10.1007/s00018-015-2110-0