Interactions between p-Akt and Smad3 in injured muscles initiate myogenesis or fibrogenesis
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Publication Date: | 2013 |
Other Authors: | , , , , , |
Format: | Article |
Language: | eng |
Source: | Repositório Institucional da UNIFESP |
Download full: | http://repositorio.unifesp.br/handle/11600/36564 http://dx.doi.org/10.1152/ajpendo.00644.2012 |
Summary: | In catabolic conditions such as aging and diabetes, IGF signaling is impaired and fibrosis develops in skeletal muscles. To examine whether impaired IGF signaling initiates muscle fibrosis, we generated IGF-IR+/- heterozygous mice by crossing loxP-floxed IGF-IR (exon 3) mice with MyoD-cre mice. IGF-IR+/- mice were studied because we were unable to obtain homozygous IGF-IR-KO mice. in IGF-IR+/- mice, both growth and expression of myogenic genes (MyoD and myogenin; markers of satellite cell proliferation and differentiation, respectively) were depressed. Likewise, in injured muscles of IGF-IR+/- mice, there was impaired regeneration, depressed expression of MyoD and myogenin, and increased expression of TGF-beta 1, alpha-SMA, collagen I, and fibrosis. To uncover mechanisms stimulating fibrosis, we isolated satellite cells from muscles of IGF-IR+/- mice and found reduced proliferation and differentiation plus increased TGF-beta 1 production. in C2C12 myoblasts (a model of satellite cells), IGF-I treatment inhibited TGF-beta 1-stimulated Smad3 phosphorylation, its nuclear translocation, and expression of fibronectin. Using immunoprecipitation assay, we found an interaction between p-Akt or Akt with Smad3 in wild-type mouse muscles and in C2C12 myoblasts; importantly, IGF-I increased p-Akt and Smad3 interaction, whereas TGF-beta 1 decreased it. Therefore, in muscles of IGF-IR+/- mice, the reduction in IGF-IR reduces p-Akt, allowing for dissociation and nuclear translocation of Smad3 to enhance the TGF-beta 1 signaling pathway, leading to fibrosis. Thus, strategies to improve IGF signaling could prevent fibrosis in catabolic conditions with impaired IGF signaling. |
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Dong, YanjunLakhia, RonakThomas, Sandhya S.Dong, YanlanWang, Xiaonan H.Santos Silva, Kleiton Augusto [UNIFESP]Zhang, LipingBaylor Coll MedEmory UnivCapital Med UnivUniversidade Federal de São Paulo (UNIFESP)2016-01-24T14:32:01Z2016-01-24T14:32:01Z2013-08-01American Journal of Physiology-endocrinology and Metabolism. Bethesda: Amer Physiological Soc, v. 305, n. 3, p. E367-E375, 2013.0193-1849http://repositorio.unifesp.br/handle/11600/36564http://dx.doi.org/10.1152/ajpendo.00644.201210.1152/ajpendo.00644.2012WOS:000322701700006In catabolic conditions such as aging and diabetes, IGF signaling is impaired and fibrosis develops in skeletal muscles. To examine whether impaired IGF signaling initiates muscle fibrosis, we generated IGF-IR+/- heterozygous mice by crossing loxP-floxed IGF-IR (exon 3) mice with MyoD-cre mice. IGF-IR+/- mice were studied because we were unable to obtain homozygous IGF-IR-KO mice. in IGF-IR+/- mice, both growth and expression of myogenic genes (MyoD and myogenin; markers of satellite cell proliferation and differentiation, respectively) were depressed. Likewise, in injured muscles of IGF-IR+/- mice, there was impaired regeneration, depressed expression of MyoD and myogenin, and increased expression of TGF-beta 1, alpha-SMA, collagen I, and fibrosis. To uncover mechanisms stimulating fibrosis, we isolated satellite cells from muscles of IGF-IR+/- mice and found reduced proliferation and differentiation plus increased TGF-beta 1 production. in C2C12 myoblasts (a model of satellite cells), IGF-I treatment inhibited TGF-beta 1-stimulated Smad3 phosphorylation, its nuclear translocation, and expression of fibronectin. Using immunoprecipitation assay, we found an interaction between p-Akt or Akt with Smad3 in wild-type mouse muscles and in C2C12 myoblasts; importantly, IGF-I increased p-Akt and Smad3 interaction, whereas TGF-beta 1 decreased it. Therefore, in muscles of IGF-IR+/- mice, the reduction in IGF-IR reduces p-Akt, allowing for dissociation and nuclear translocation of Smad3 to enhance the TGF-beta 1 signaling pathway, leading to fibrosis. Thus, strategies to improve IGF signaling could prevent fibrosis in catabolic conditions with impaired IGF signaling.Satellite HealthAmerican Diabetes AssociationNational Institute of Diabetes and Digestive and Kidney DiseasesBaylor Coll Med, Div Nephrol, Dept Med, Houston, TX 77030 USAEmory Univ, Dept Med, Div Renal, Atlanta, GA 30322 USACapital Med Univ, Beijing An Zhen Hosp, Beijing Inst Heart Lung & Blood Vessel Dis, Beijing, Peoples R ChinaUniversidade Federal de São Paulo, Div Nephrol, Dept Med, São Paulo, BrazilUniversidade Federal de São Paulo, Div Nephrol, Dept Med, São Paulo, BrazilAmerican Diabetes Association: 1-11-BS-194National Institute of Diabetes and Digestive and Kidney Diseases: R37-DK-37175National Institute of Diabetes and Digestive and Kidney Diseases: T32-DK-62706Web of ScienceE367-E375engAmer Physiological SocAmerican Journal of Physiology-endocrinology and Metabolismtransforming growth factor-beta 1insulin-like growth factor Isatellite cellsmyogenesisfibrosisSmad3Interactions between p-Akt and Smad3 in injured muscles initiate myogenesis or fibrogenesisinfo:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/articleinfo:eu-repo/semantics/openAccessreponame:Repositório Institucional da UNIFESPinstname:Universidade Federal de São Paulo (UNIFESP)instacron:UNIFESP11600/365642022-11-04 15:08:28.399metadata only accessoai:repositorio.unifesp.br:11600/36564Repositório InstitucionalPUBhttp://www.repositorio.unifesp.br/oai/requestopendoar:34652022-11-04T18:08:28Repositório Institucional da UNIFESP - Universidade Federal de São Paulo (UNIFESP)false |
dc.title.en.fl_str_mv |
Interactions between p-Akt and Smad3 in injured muscles initiate myogenesis or fibrogenesis |
title |
Interactions between p-Akt and Smad3 in injured muscles initiate myogenesis or fibrogenesis |
spellingShingle |
Interactions between p-Akt and Smad3 in injured muscles initiate myogenesis or fibrogenesis Dong, Yanjun transforming growth factor-beta 1 insulin-like growth factor I satellite cells myogenesis fibrosis Smad3 |
title_short |
Interactions between p-Akt and Smad3 in injured muscles initiate myogenesis or fibrogenesis |
title_full |
Interactions between p-Akt and Smad3 in injured muscles initiate myogenesis or fibrogenesis |
title_fullStr |
Interactions between p-Akt and Smad3 in injured muscles initiate myogenesis or fibrogenesis |
title_full_unstemmed |
Interactions between p-Akt and Smad3 in injured muscles initiate myogenesis or fibrogenesis |
title_sort |
Interactions between p-Akt and Smad3 in injured muscles initiate myogenesis or fibrogenesis |
author |
Dong, Yanjun |
author_facet |
Dong, Yanjun Lakhia, Ronak Thomas, Sandhya S. Dong, Yanlan Wang, Xiaonan H. Santos Silva, Kleiton Augusto [UNIFESP] Zhang, Liping |
author_role |
author |
author2 |
Lakhia, Ronak Thomas, Sandhya S. Dong, Yanlan Wang, Xiaonan H. Santos Silva, Kleiton Augusto [UNIFESP] Zhang, Liping |
author2_role |
author author author author author author |
dc.contributor.institution.none.fl_str_mv |
Baylor Coll Med Emory Univ Capital Med Univ Universidade Federal de São Paulo (UNIFESP) |
dc.contributor.author.fl_str_mv |
Dong, Yanjun Lakhia, Ronak Thomas, Sandhya S. Dong, Yanlan Wang, Xiaonan H. Santos Silva, Kleiton Augusto [UNIFESP] Zhang, Liping |
dc.subject.eng.fl_str_mv |
transforming growth factor-beta 1 insulin-like growth factor I satellite cells myogenesis fibrosis Smad3 |
topic |
transforming growth factor-beta 1 insulin-like growth factor I satellite cells myogenesis fibrosis Smad3 |
description |
In catabolic conditions such as aging and diabetes, IGF signaling is impaired and fibrosis develops in skeletal muscles. To examine whether impaired IGF signaling initiates muscle fibrosis, we generated IGF-IR+/- heterozygous mice by crossing loxP-floxed IGF-IR (exon 3) mice with MyoD-cre mice. IGF-IR+/- mice were studied because we were unable to obtain homozygous IGF-IR-KO mice. in IGF-IR+/- mice, both growth and expression of myogenic genes (MyoD and myogenin; markers of satellite cell proliferation and differentiation, respectively) were depressed. Likewise, in injured muscles of IGF-IR+/- mice, there was impaired regeneration, depressed expression of MyoD and myogenin, and increased expression of TGF-beta 1, alpha-SMA, collagen I, and fibrosis. To uncover mechanisms stimulating fibrosis, we isolated satellite cells from muscles of IGF-IR+/- mice and found reduced proliferation and differentiation plus increased TGF-beta 1 production. in C2C12 myoblasts (a model of satellite cells), IGF-I treatment inhibited TGF-beta 1-stimulated Smad3 phosphorylation, its nuclear translocation, and expression of fibronectin. Using immunoprecipitation assay, we found an interaction between p-Akt or Akt with Smad3 in wild-type mouse muscles and in C2C12 myoblasts; importantly, IGF-I increased p-Akt and Smad3 interaction, whereas TGF-beta 1 decreased it. Therefore, in muscles of IGF-IR+/- mice, the reduction in IGF-IR reduces p-Akt, allowing for dissociation and nuclear translocation of Smad3 to enhance the TGF-beta 1 signaling pathway, leading to fibrosis. Thus, strategies to improve IGF signaling could prevent fibrosis in catabolic conditions with impaired IGF signaling. |
publishDate |
2013 |
dc.date.issued.fl_str_mv |
2013-08-01 |
dc.date.accessioned.fl_str_mv |
2016-01-24T14:32:01Z |
dc.date.available.fl_str_mv |
2016-01-24T14:32:01Z |
dc.type.status.fl_str_mv |
info:eu-repo/semantics/publishedVersion |
dc.type.driver.fl_str_mv |
info:eu-repo/semantics/article |
format |
article |
status_str |
publishedVersion |
dc.identifier.citation.fl_str_mv |
American Journal of Physiology-endocrinology and Metabolism. Bethesda: Amer Physiological Soc, v. 305, n. 3, p. E367-E375, 2013. |
dc.identifier.uri.fl_str_mv |
http://repositorio.unifesp.br/handle/11600/36564 http://dx.doi.org/10.1152/ajpendo.00644.2012 |
dc.identifier.issn.none.fl_str_mv |
0193-1849 |
dc.identifier.doi.none.fl_str_mv |
10.1152/ajpendo.00644.2012 |
dc.identifier.wos.none.fl_str_mv |
WOS:000322701700006 |
identifier_str_mv |
American Journal of Physiology-endocrinology and Metabolism. Bethesda: Amer Physiological Soc, v. 305, n. 3, p. E367-E375, 2013. 0193-1849 10.1152/ajpendo.00644.2012 WOS:000322701700006 |
url |
http://repositorio.unifesp.br/handle/11600/36564 http://dx.doi.org/10.1152/ajpendo.00644.2012 |
dc.language.iso.fl_str_mv |
eng |
language |
eng |
dc.relation.ispartof.none.fl_str_mv |
American Journal of Physiology-endocrinology and Metabolism |
dc.rights.driver.fl_str_mv |
info:eu-repo/semantics/openAccess |
eu_rights_str_mv |
openAccess |
dc.format.none.fl_str_mv |
E367-E375 |
dc.publisher.none.fl_str_mv |
Amer Physiological Soc |
publisher.none.fl_str_mv |
Amer Physiological Soc |
dc.source.none.fl_str_mv |
reponame:Repositório Institucional da UNIFESP instname:Universidade Federal de São Paulo (UNIFESP) instacron:UNIFESP |
instname_str |
Universidade Federal de São Paulo (UNIFESP) |
instacron_str |
UNIFESP |
institution |
UNIFESP |
reponame_str |
Repositório Institucional da UNIFESP |
collection |
Repositório Institucional da UNIFESP |
repository.name.fl_str_mv |
Repositório Institucional da UNIFESP - Universidade Federal de São Paulo (UNIFESP) |
repository.mail.fl_str_mv |
|
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1802764184241307648 |