α-smooth muscle actin is not a marker of fibrogenic cell activity in skeletal muscle fibrosis.

α-Smooth muscle actin (α-SMA) is used as a marker for a subset of activated fibrogenic cells, myofibroblasts, which are regarded as important effector cells of tissue fibrogenesis. We address whether α-SMA-expressing myofibroblasts are detectable in fibrotic muscles of mdx5cv mice, a mouse model for...

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Main Authors: Wanming Zhao, Xingyu Wang, Kai-Hui Sun, Lan Zhou
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2018-01-01
Series:PLoS ONE
Online Access:http://europepmc.org/articles/PMC5761950?pdf=render
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author Wanming Zhao
Xingyu Wang
Kai-Hui Sun
Lan Zhou
author_facet Wanming Zhao
Xingyu Wang
Kai-Hui Sun
Lan Zhou
author_sort Wanming Zhao
collection DOAJ
description α-Smooth muscle actin (α-SMA) is used as a marker for a subset of activated fibrogenic cells, myofibroblasts, which are regarded as important effector cells of tissue fibrogenesis. We address whether α-SMA-expressing myofibroblasts are detectable in fibrotic muscles of mdx5cv mice, a mouse model for Duchenne muscular dystrophy (DMD), and whether the α-SMA expression correlates with the fibrogenic function of intramuscular fibrogenic cells. α-SMA immunostaining signal was not detected in collagen I (GFP)-expressing cells in fibrotic muscles of ColI-GFP/mdx5cv mice, but it was readily detected in smooth muscle cells lining intramuscular blood vessel walls. α-SMA expression was detected by quantitative RT-PCR and Western blot in fibrogenic cells sorted from diaphragm and quadriceps muscles of the ColI-GFP/mdx5cv mice. Consistent with the more severe fibrosis in the ColI-GFP/mdx5cv diaphragm, the fibrogenic cells in the diaphragm exerted a stronger fibrogenic function than the fibrogenic cells in the quadriceps as gauged by their extracellular matrix gene expression. However, both gene and protein expression of α-SMA was lower in the diaphragm fibrogenic cells than in the quadriceps fibrogenic cells in the ColI-GFP/mdx5cv mice. We conclude that myofibroblasts are present in fibrotic skeletal muscles, but their expression of α-SMA is not detectable by immunostaining. The level of α-SMA expression by intramuscular fibrogenic cells does not correlate positively with the level of collagen gene expression or the severity of skeletal muscle fibrosis in the mdx5cv mice. α-SMA is not a functional marker of fibrogenic cells in skeletal muscle fibrosis associated with muscular dystrophy.
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spelling doaj.art-a954950eed8148f7b3a5d673fca8a0162022-12-22T01:13:56ZengPublic Library of Science (PLoS)PLoS ONE1932-62032018-01-01131e019103110.1371/journal.pone.0191031α-smooth muscle actin is not a marker of fibrogenic cell activity in skeletal muscle fibrosis.Wanming ZhaoXingyu WangKai-Hui SunLan Zhouα-Smooth muscle actin (α-SMA) is used as a marker for a subset of activated fibrogenic cells, myofibroblasts, which are regarded as important effector cells of tissue fibrogenesis. We address whether α-SMA-expressing myofibroblasts are detectable in fibrotic muscles of mdx5cv mice, a mouse model for Duchenne muscular dystrophy (DMD), and whether the α-SMA expression correlates with the fibrogenic function of intramuscular fibrogenic cells. α-SMA immunostaining signal was not detected in collagen I (GFP)-expressing cells in fibrotic muscles of ColI-GFP/mdx5cv mice, but it was readily detected in smooth muscle cells lining intramuscular blood vessel walls. α-SMA expression was detected by quantitative RT-PCR and Western blot in fibrogenic cells sorted from diaphragm and quadriceps muscles of the ColI-GFP/mdx5cv mice. Consistent with the more severe fibrosis in the ColI-GFP/mdx5cv diaphragm, the fibrogenic cells in the diaphragm exerted a stronger fibrogenic function than the fibrogenic cells in the quadriceps as gauged by their extracellular matrix gene expression. However, both gene and protein expression of α-SMA was lower in the diaphragm fibrogenic cells than in the quadriceps fibrogenic cells in the ColI-GFP/mdx5cv mice. We conclude that myofibroblasts are present in fibrotic skeletal muscles, but their expression of α-SMA is not detectable by immunostaining. The level of α-SMA expression by intramuscular fibrogenic cells does not correlate positively with the level of collagen gene expression or the severity of skeletal muscle fibrosis in the mdx5cv mice. α-SMA is not a functional marker of fibrogenic cells in skeletal muscle fibrosis associated with muscular dystrophy.http://europepmc.org/articles/PMC5761950?pdf=render
spellingShingle Wanming Zhao
Xingyu Wang
Kai-Hui Sun
Lan Zhou
α-smooth muscle actin is not a marker of fibrogenic cell activity in skeletal muscle fibrosis.
PLoS ONE
title α-smooth muscle actin is not a marker of fibrogenic cell activity in skeletal muscle fibrosis.
title_full α-smooth muscle actin is not a marker of fibrogenic cell activity in skeletal muscle fibrosis.
title_fullStr α-smooth muscle actin is not a marker of fibrogenic cell activity in skeletal muscle fibrosis.
title_full_unstemmed α-smooth muscle actin is not a marker of fibrogenic cell activity in skeletal muscle fibrosis.
title_short α-smooth muscle actin is not a marker of fibrogenic cell activity in skeletal muscle fibrosis.
title_sort α smooth muscle actin is not a marker of fibrogenic cell activity in skeletal muscle fibrosis
url http://europepmc.org/articles/PMC5761950?pdf=render
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AT kaihuisun asmoothmuscleactinisnotamarkeroffibrogeniccellactivityinskeletalmusclefibrosis
AT lanzhou asmoothmuscleactinisnotamarkeroffibrogeniccellactivityinskeletalmusclefibrosis