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פותח על ידי קלירמאש פתרונות בע"מ -
Halofuginone improves muscle-cell survival in muscular dystrophies
Year:
2014
Authors :
גנין, אולגה
;
.
לוי, אשרת
;
.
פינס, מרק
;
.
Volume :
1843
Co-Authors:
Bodanovsky, A., Department of Animal Sciences, The Hebrew University of Jerusalem, Rehovot 76100, Israel
Guttman, N., Department of Animal Sciences, The Hebrew University of Jerusalem, Rehovot 76100, Israel
Barzilai-Tutsch, H., Department of Animal Sciences, The Hebrew University of Jerusalem, Rehovot 76100, Israel
Genin, O., Institute of Animal Science, The Volcani Center, Bet Dagan 52505, Israel
Levy, O., Institute of Animal Science, The Volcani Center, Bet Dagan 52505, Israel
Pines, M., Institute of Animal Science, The Volcani Center, Bet Dagan 52505, Israel
Halevy, O., Department of Animal Sciences, The Hebrew University of Jerusalem, Rehovot 76100, Israel
Facilitators :
From page:
1339
To page:
1347
(
Total pages:
9
)
Abstract:
Halofuginone has been shown to prevent fibrosis via the transforming growth factor-β/Smad3 pathway in muscular dystrophies. We hypothesized that halofuginone would reduce apoptosis-the presumed cause of satellite-cell depletion during muscle degradation-in the mdx mouse model of Duchenne muscular dystrophy. Six-week-old mdx mouse diaphragm exhibited fourfold higher numbers of apoptotic nuclei compared with wild-type mice as determined by a TUNEL assay. Apoptotic nuclei were found in macrophages and in Pax7-expressing cells; some were located in centrally-nucleated regenerating myofibers. Halofuginone treatment of mdx mice reduced the apoptotic nuclei number in the diaphragm, together with reduction in Bax and induction in Bcl2 levels in myofibers isolated from these mice. A similar effect was observed when halofuginone was added to cultured myofibers. No apparent effect of halofuginone was observed in wild-type mice. Inhibition of apoptosis or staurosporine-induced apoptosis by halofuginone in mdx primary myoblasts and C2 myogenic cell line, respectively, was reflected by less pyknotic/apoptotic cells and reduced Bax expression. This reduction was reversed by a phosphinositide-3-kinase and mitogen-activated protein kinase/extracellular signal-regulated protein kinase inhibitors, suggesting involvement of these pathways in mediating halofuginone's effects on apoptosis. Halofuginone increased apoptosis in α smooth muscle actin- and prolyl 4-hydroxylase β-expressing cells in mdx diaphragm and in myofibroblasts, the major source of extracellular matrix. The data suggest an additional mechanism by which halofuginone improves muscle pathology and function in muscular dystrophies. © 2014 Elsevier B.V.
Note:
Related Files :
Animal
Animals
apoptosis
Genetics
metabolism
mice
Pathology
עוד תגיות
תוכן קשור
More details
DOI :
10.1016/j.bbamcr.2014.03.025
Article number:
Affiliations:
Database:
סקופוס
Publication Type:
מאמר
;
.
Language:
אנגלית
Editors' remarks:
ID:
26985
Last updated date:
02/03/2022 17:27
Creation date:
17/04/2018 00:27
Scientific Publication
Halofuginone improves muscle-cell survival in muscular dystrophies
1843
Bodanovsky, A., Department of Animal Sciences, The Hebrew University of Jerusalem, Rehovot 76100, Israel
Guttman, N., Department of Animal Sciences, The Hebrew University of Jerusalem, Rehovot 76100, Israel
Barzilai-Tutsch, H., Department of Animal Sciences, The Hebrew University of Jerusalem, Rehovot 76100, Israel
Genin, O., Institute of Animal Science, The Volcani Center, Bet Dagan 52505, Israel
Levy, O., Institute of Animal Science, The Volcani Center, Bet Dagan 52505, Israel
Pines, M., Institute of Animal Science, The Volcani Center, Bet Dagan 52505, Israel
Halevy, O., Department of Animal Sciences, The Hebrew University of Jerusalem, Rehovot 76100, Israel
Halofuginone improves muscle-cell survival in muscular dystrophies
Halofuginone has been shown to prevent fibrosis via the transforming growth factor-β/Smad3 pathway in muscular dystrophies. We hypothesized that halofuginone would reduce apoptosis-the presumed cause of satellite-cell depletion during muscle degradation-in the mdx mouse model of Duchenne muscular dystrophy. Six-week-old mdx mouse diaphragm exhibited fourfold higher numbers of apoptotic nuclei compared with wild-type mice as determined by a TUNEL assay. Apoptotic nuclei were found in macrophages and in Pax7-expressing cells; some were located in centrally-nucleated regenerating myofibers. Halofuginone treatment of mdx mice reduced the apoptotic nuclei number in the diaphragm, together with reduction in Bax and induction in Bcl2 levels in myofibers isolated from these mice. A similar effect was observed when halofuginone was added to cultured myofibers. No apparent effect of halofuginone was observed in wild-type mice. Inhibition of apoptosis or staurosporine-induced apoptosis by halofuginone in mdx primary myoblasts and C2 myogenic cell line, respectively, was reflected by less pyknotic/apoptotic cells and reduced Bax expression. This reduction was reversed by a phosphinositide-3-kinase and mitogen-activated protein kinase/extracellular signal-regulated protein kinase inhibitors, suggesting involvement of these pathways in mediating halofuginone's effects on apoptosis. Halofuginone increased apoptosis in α smooth muscle actin- and prolyl 4-hydroxylase β-expressing cells in mdx diaphragm and in myofibroblasts, the major source of extracellular matrix. The data suggest an additional mechanism by which halofuginone improves muscle pathology and function in muscular dystrophies. © 2014 Elsevier B.V.
Scientific Publication
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