Cargando…

Stem Cell Antigen-1 in Skeletal Muscle Function

Stem cell antigen-1 (Sca-1) is a member of the Ly-6 multigene family encoding highly homologous, glycosyl-phosphatidylinositol-anchored membrane proteins. Sca-1 is expressed on muscle-derived stem cells and myogenic precursors recruited to sites of muscle injury. We previously reported that inhibiti...

Descripción completa

Detalles Bibliográficos
Autores principales: Bernstein, Harold S., Samad, Tahmina, Cholsiripunlert, Sompob, Khalifian, Saami, Gong, Wenhui, Ritner, Carissa, Aurigui, Julian, Ling, Vivian, Wilschut, Karlijn J., Bennett, Stephen, Hoffman, Julien, Oishi, Peter
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3770837/
https://www.ncbi.nlm.nih.gov/pubmed/24042315
http://dx.doi.org/10.1371/currents.md.411a8332d61e22725e6937b97e6d0ef8
_version_ 1782284146117181440
author Bernstein, Harold S.
Samad, Tahmina
Cholsiripunlert, Sompob
Khalifian, Saami
Gong, Wenhui
Ritner, Carissa
Aurigui, Julian
Ling, Vivian
Wilschut, Karlijn J.
Bennett, Stephen
Hoffman, Julien
Oishi, Peter
author_facet Bernstein, Harold S.
Samad, Tahmina
Cholsiripunlert, Sompob
Khalifian, Saami
Gong, Wenhui
Ritner, Carissa
Aurigui, Julian
Ling, Vivian
Wilschut, Karlijn J.
Bennett, Stephen
Hoffman, Julien
Oishi, Peter
author_sort Bernstein, Harold S.
collection PubMed
description Stem cell antigen-1 (Sca-1) is a member of the Ly-6 multigene family encoding highly homologous, glycosyl-phosphatidylinositol-anchored membrane proteins. Sca-1 is expressed on muscle-derived stem cells and myogenic precursors recruited to sites of muscle injury. We previously reported that inhibition of Sca-1 expression stimulated myoblast proliferation in vitro and regulated the tempo of muscle repair in vivo. Despite its function in myoblast expansion during muscle repair, a role for Sca-1 in normal, post-natal muscle has not been thoroughly investigated. We systematically compared Sca-1-/- (KO) and Sca-1+/+ (WT) mice and hindlimb muscles to elucidate the tissue, contractile, and functional effects of Sca-1 in young and aging animals. Comparison of muscle volume, fibrosis, myofiber cross-sectional area, and Pax7+ myoblast number showed little differences between ages or genotypes. Exercise protocols, however, demonstrated decreased stamina in KO versus WT mice, with young KO mice achieving results similar to aging WT animals. In addition, KO mice did not improve with practice, while WT animals demonstrated conditioning over time. Surprisingly, myomechanical analysis of isolated muscles showed that KO young muscle generated more force and experienced less fatigue. However, KO muscle also demonstrated incomplete relaxation with fatigue. These findings suggest that Sca-1 is necessary for muscle conditioning with exercise, and that deficient conditioning in Sca-1 KO animals becomes more pronounced with age.
format Online
Article
Text
id pubmed-3770837
institution National Center for Biotechnology Information
language English
publishDate 2013
publisher Public Library of Science
record_format MEDLINE/PubMed
spelling pubmed-37708372013-09-15 Stem Cell Antigen-1 in Skeletal Muscle Function Bernstein, Harold S. Samad, Tahmina Cholsiripunlert, Sompob Khalifian, Saami Gong, Wenhui Ritner, Carissa Aurigui, Julian Ling, Vivian Wilschut, Karlijn J. Bennett, Stephen Hoffman, Julien Oishi, Peter PLoS Curr Animal Models Stem cell antigen-1 (Sca-1) is a member of the Ly-6 multigene family encoding highly homologous, glycosyl-phosphatidylinositol-anchored membrane proteins. Sca-1 is expressed on muscle-derived stem cells and myogenic precursors recruited to sites of muscle injury. We previously reported that inhibition of Sca-1 expression stimulated myoblast proliferation in vitro and regulated the tempo of muscle repair in vivo. Despite its function in myoblast expansion during muscle repair, a role for Sca-1 in normal, post-natal muscle has not been thoroughly investigated. We systematically compared Sca-1-/- (KO) and Sca-1+/+ (WT) mice and hindlimb muscles to elucidate the tissue, contractile, and functional effects of Sca-1 in young and aging animals. Comparison of muscle volume, fibrosis, myofiber cross-sectional area, and Pax7+ myoblast number showed little differences between ages or genotypes. Exercise protocols, however, demonstrated decreased stamina in KO versus WT mice, with young KO mice achieving results similar to aging WT animals. In addition, KO mice did not improve with practice, while WT animals demonstrated conditioning over time. Surprisingly, myomechanical analysis of isolated muscles showed that KO young muscle generated more force and experienced less fatigue. However, KO muscle also demonstrated incomplete relaxation with fatigue. These findings suggest that Sca-1 is necessary for muscle conditioning with exercise, and that deficient conditioning in Sca-1 KO animals becomes more pronounced with age. Public Library of Science 2013-08-15 /pmc/articles/PMC3770837/ /pubmed/24042315 http://dx.doi.org/10.1371/currents.md.411a8332d61e22725e6937b97e6d0ef8 Text en http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Animal Models
Bernstein, Harold S.
Samad, Tahmina
Cholsiripunlert, Sompob
Khalifian, Saami
Gong, Wenhui
Ritner, Carissa
Aurigui, Julian
Ling, Vivian
Wilschut, Karlijn J.
Bennett, Stephen
Hoffman, Julien
Oishi, Peter
Stem Cell Antigen-1 in Skeletal Muscle Function
title Stem Cell Antigen-1 in Skeletal Muscle Function
title_full Stem Cell Antigen-1 in Skeletal Muscle Function
title_fullStr Stem Cell Antigen-1 in Skeletal Muscle Function
title_full_unstemmed Stem Cell Antigen-1 in Skeletal Muscle Function
title_short Stem Cell Antigen-1 in Skeletal Muscle Function
title_sort stem cell antigen-1 in skeletal muscle function
topic Animal Models
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3770837/
https://www.ncbi.nlm.nih.gov/pubmed/24042315
http://dx.doi.org/10.1371/currents.md.411a8332d61e22725e6937b97e6d0ef8
work_keys_str_mv AT bernsteinharolds stemcellantigen1inskeletalmusclefunction
AT samadtahmina stemcellantigen1inskeletalmusclefunction
AT cholsiripunlertsompob stemcellantigen1inskeletalmusclefunction
AT khalifiansaami stemcellantigen1inskeletalmusclefunction
AT gongwenhui stemcellantigen1inskeletalmusclefunction
AT ritnercarissa stemcellantigen1inskeletalmusclefunction
AT auriguijulian stemcellantigen1inskeletalmusclefunction
AT lingvivian stemcellantigen1inskeletalmusclefunction
AT wilschutkarlijnj stemcellantigen1inskeletalmusclefunction
AT bennettstephen stemcellantigen1inskeletalmusclefunction
AT hoffmanjulien stemcellantigen1inskeletalmusclefunction
AT oishipeter stemcellantigen1inskeletalmusclefunction