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[title] => [Highly efficient, functional engraftment of skeletal muscle stem cells in dystrophic muscles.]
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<div class="biblio_authors"><h3>Authors:</h3> <a href="/biblio/author/Cerletti+M">Cerletti M , Jurga S , Witczak CA , Hirshman MF , Shadrach JL , Goodyear LJ , Wagers AJ ,</a></div>
<div class="biblio_source"><h3>Source: </h3> Cell, Volume 134, p.37-47 (2008)</div>
<h3>URL:</h3><a href="http://linkinghub.elsevier.com/retrieve/pii/S0092-8674(08)00755-1">http://linkinghub.elsevier.com/retrieve/pii/S0092-8674(08)00755-1</a>
<h3>Abstract:</h3> <p>Satellite cells reside beneath the basal lamina of skeletal muscle fibers and include cells that act as precursors for muscle growth and repair. Although they share a common anatomical localization and typically are considered a homogeneous population, satellite cells actually exhibit substantial heterogeneity. We used cell-surface marker expression to purify from the satellite cell pool a distinct population of skeletal muscle precursors (SMPs) that function as muscle stem cells. When engrafted into muscle of dystrophin-deficient mdx mice, purified SMPs contributed to up to 94% of myofibers, restoring dystrophin expression and significantly improving muscle histology and contractile function. Transplanted SMPs also entered the satellite cell compartment, renewing the endogenous stem cell pool and participating in subsequent rounds of injury repair. Together, these studies indicate the presence in adult skeletal muscle of prospectively isolatable muscle-forming stem cells and directly demonstrate the efficacy of myogenic stem cell transplant for treating muscle degenerative disease.</p>
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[biblio_abst_e] => [<p>Satellite cells reside beneath the basal lamina of skeletal muscle fibers and include cells that act as precursors for muscle growth and repair. Although they share a common anatomical localization and typically are considered a homogeneous population, satellite cells actually exhibit substantial heterogeneity. We used cell-surface marker expression to purify from the satellite cell pool a distinct population of skeletal muscle precursors (SMPs) that function as muscle stem cells. When engrafted into muscle of dystrophin-deficient mdx mice, purified SMPs contributed to up to 94% of myofibers, restoring dystrophin expression and significantly improving muscle histology and contractile function. Transplanted SMPs also entered the satellite cell compartment, renewing the endogenous stem cell pool and participating in subsequent rounds of injury repair. Together, these studies indicate the presence in adult skeletal muscle of prospectively isolatable muscle-forming stem cells and directly demonstrate the efficacy of myogenic stem cell transplant for treating muscle degenerative disease.</p>]
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<div class="biblio_authors"><h3>Authors:</h3> <a href="/biblio/author/Cerletti+M">Cerletti M , Jurga S , Witczak CA , Hirshman MF , Shadrach JL , Goodyear LJ , Wagers AJ ,</a></div>
<div class="biblio_source"><h3>Source: </h3> Cell, Volume 134, p.37-47 (2008)</div>
<h3>URL:</h3><a href="http://linkinghub.elsevier.com/retrieve/pii/S0092-8674(08)00755-1">http://linkinghub.elsevier.com/retrieve/pii/S0092-8674(08)00755-1</a>
<h3>Abstract:</h3> <p>Satellite cells reside beneath the basal lamina of skeletal muscle fibers and include cells that act as precursors for muscle growth and repair. Although they share a common anatomical localization and typically are considered a homogeneous population, satellite cells actually exhibit substantial heterogeneity. We used cell-surface marker expression to purify from the satellite cell pool a distinct population of skeletal muscle precursors (SMPs) that function as muscle stem cells. When engrafted into muscle of dystrophin-deficient mdx mice, purified SMPs contributed to up to 94% of myofibers, restoring dystrophin expression and significantly improving muscle histology and contractile function. Transplanted SMPs also entered the satellite cell compartment, renewing the endogenous stem cell pool and participating in subsequent rounds of injury repair. Together, these studies indicate the presence in adult skeletal muscle of prospectively isolatable muscle-forming stem cells and directly demonstrate the efficacy of myogenic stem cell transplant for treating muscle degenerative disease.</p>
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<div class="biblio_authors"><h3>Authors:</h3> <a href="/biblio/author/Cerletti+M">Cerletti M , Jurga S , Witczak CA , Hirshman MF , Shadrach JL , Goodyear LJ , Wagers AJ ,</a></div>
<div class="biblio_source"><h3>Source: </h3> Cell, Volume 134, p.37-47 (2008)</div>
<h3>URL:</h3><a href="http://linkinghub.elsevier.com/retrieve/pii/S0092-8674(08)00755-1">http://linkinghub.elsevier.com/retrieve/pii/S0092-8674(08)00755-1</a>
<h3>Abstract:</h3> <p>Satellite cells reside beneath the basal lamina of skeletal muscle fibers and include cells that act as precursors for muscle growth and repair. Although they share a common anatomical localization and typically are considered a homogeneous population, satellite cells actually exhibit substantial heterogeneity. We used cell-surface marker expression to purify from the satellite cell pool a distinct population of skeletal muscle precursors (SMPs) that function as muscle stem cells. When engrafted into muscle of dystrophin-deficient mdx mice, purified SMPs contributed to up to 94% of myofibers, restoring dystrophin expression and significantly improving muscle histology and contractile function. Transplanted SMPs also entered the satellite cell compartment, renewing the endogenous stem cell pool and participating in subsequent rounds of injury repair. Together, these studies indicate the presence in adult skeletal muscle of prospectively isolatable muscle-forming stem cells and directly demonstrate the efficacy of myogenic stem cell transplant for treating muscle degenerative disease.</p>
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