Early Life Nutrition Modulates Muscle Stem Cell Number: Implications for Muscle Mass and Repair

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Early Life Nutrition Modulates Muscle Stem Cell Number: Implications for Muscle Mass and Repair

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Title: Early Life Nutrition Modulates Muscle Stem Cell Number: Implications for Muscle Mass and Repair
Author: Woo, Melissa; Isganaitis, Elvira; Cerletti, Massimiliano; Fitzpatrick, Connor; Wagers, Amy Jo; Jimenez-Chillaron, Jose; Patti, Mary-Elizabeth

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Citation: Woo, Melissa, Elvira Isganaitis, Massimiliano Cerletti, Connor Fitzpatrick, Amy J. Wagers, Jose Jimenez-Chillaron, and Mary Elizabeth Patti. 2011. Early life nutrition modulates muscle stem cell number: implications for muscle mass and repair. Stem Cells and Development 20(10): 1763-1769.
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Abstract: Suboptimal nutrition during prenatal and early postnatal development is associated with increased risk for type 2 diabetes during adult life. A hallmark of such diabetes risk is altered body composition, including reduced lean mass and increased adiposity. Since stem cell number and activity are important determinants of muscle mass, modulation of perinatal nutrition could alter stem cell number/function, potentially mediating developmentally programmed reductions in muscle mass. Skeletal muscle precursors (SMP) were purified from muscle of mice subjected to prenatal undernutrition and/or early postnatal high-fat diet (HFD)—experimental models that are both associated with obesity and diabetes risk. SMP number was determined by flow cytometry, proliferative capacity measured in vitro, and regenerative capacity of these cells determined in vivo after muscle freeze injury. Prenatally undernutrition (UN) mice showed significantly reduced SMP frequencies [Control (C) \(4.8\%\pm0.3\%\) (% live cells) vs. UN \(3.2\%\pm0.4\%, P = 0.015\)] at 6 weeks; proliferative capacity was unaltered. Reduced SMP in UN was associated with 32% decrease in regeneration after injury (\(C 16\%\pm3\%\) of injured area vs. \(UN 11\%\pm2\%; P < 0.0001\)). SMP frequency was also reduced in HFD-fed mice (chow \(6.4\%\pm0.6\% vs. HFD 4.7\% \pm0.4\%, P = 0.03\)), and associated with \(44\%\) decreased regeneration (chow \(16\%\pm2.7\% vs. HFD 9\%\pm2.2\%; P < 0.0001\)). Prenatal undernutrition was additive with postnatal HFD. Thus, both prenatal undernutrition and postnatal overnutrition reduce myogenic stem cell frequency and function, indicating that developmentally established differences in muscle-resident stem cell populations may provoke reductions in muscle mass and repair and contribute to diabetes risk.
Published Version: DOI: 10.1089/scd.2010.0349
Other Sources: http://www.ncbi.nlm.nih.gov/pubmed/21247245
Terms of Use: This article is made available under the terms and conditions applicable to Other Posted Material, as set forth at http://nrs.harvard.edu/urn-3:HUL.InstRepos:dash.current.terms-of-use#LAA
Citable link to this page: http://nrs.harvard.edu/urn-3:HUL.InstRepos:9639970

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  • FAS Scholarly Articles [7594]
    Peer reviewed scholarly articles from the Faculty of Arts and Sciences of Harvard University
 
 

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