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An artificial niche preserves the quiescence of muscle stem cells and enhances their therapeutic efficacy.
Quarta, Marco; Brett, Jamie O; DiMarco, Rebecca; De Morree, Antoine; Boutet, Stephane C; Chacon, Robert; Gibbons, Michael C; Garcia, Victor A; Su, James; Shrager, Joseph B; Heilshorn, Sarah; Rando, Thomas A.
Affiliation
  • Quarta M; Department of Neurology and Neurological Sciences, Stanford University School of Medicine, Stanford, California, USA.
  • Brett JO; Paul F. Glenn Center for the Biology of Aging, Stanford University School of Medicine, Stanford, California, USA.
  • DiMarco R; Center for Tissue Regeneration, Repair and Restoration, Veterans Affairs Palo Alto Health Care System, Palo Alto, California, USA.
  • De Morree A; Department of Neurology and Neurological Sciences, Stanford University School of Medicine, Stanford, California, USA.
  • Boutet SC; Paul F. Glenn Center for the Biology of Aging, Stanford University School of Medicine, Stanford, California, USA.
  • Chacon R; Institute for Stem Cell Biology and Regenerative Medicine, Stanford University School of Medicine, Stanford, California, USA.
  • Gibbons MC; Department of Bioengineering, Stanford University, Stanford, California, USA.
  • Garcia VA; Department of Neurology and Neurological Sciences, Stanford University School of Medicine, Stanford, California, USA.
  • Su J; Paul F. Glenn Center for the Biology of Aging, Stanford University School of Medicine, Stanford, California, USA.
  • Shrager JB; Department of Neurology and Neurological Sciences, Stanford University School of Medicine, Stanford, California, USA.
  • Heilshorn S; Paul F. Glenn Center for the Biology of Aging, Stanford University School of Medicine, Stanford, California, USA.
  • Rando TA; Department of Neurology and Neurological Sciences, Stanford University School of Medicine, Stanford, California, USA.
Nat Biotechnol ; 34(7): 752-9, 2016 07.
Article in En | MEDLINE | ID: mdl-27240197
A promising therapeutic strategy for diverse genetic disorders involves transplantation of autologous stem cells that have been genetically corrected ex vivo. A major challenge in such approaches is a loss of stem cell potency during culture. Here we describe an artificial niche for maintaining muscle stem cells (MuSCs) in vitro in a potent, quiescent state. Using a machine learning method, we identified a molecular signature of quiescence and used it to screen for factors that could maintain mouse MuSC quiescence, thus defining a quiescence medium (QM). We also engineered muscle fibers that mimic the native myofiber of the MuSC niche. Mouse MuSCs maintained in QM on engineered fibers showed enhanced potential for engraftment, tissue regeneration and self-renewal after transplantation in mice. An artificial niche adapted to human cells similarly extended the quiescence of human MuSCs in vitro and enhanced their potency in vivo. Our approach for maintaining quiescence may be applicable to stem cells isolated from other tissues.
Subject(s)

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Tissue Preservation / Myoblasts, Skeletal / Stem Cell Niche / Batch Cell Culture Techniques / Muscle Proteins Type of study: Prognostic_studies Limits: Animals Language: En Journal: Nat Biotechnol Journal subject: BIOTECNOLOGIA Year: 2016 Type: Article Affiliation country: United States

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Tissue Preservation / Myoblasts, Skeletal / Stem Cell Niche / Batch Cell Culture Techniques / Muscle Proteins Type of study: Prognostic_studies Limits: Animals Language: En Journal: Nat Biotechnol Journal subject: BIOTECNOLOGIA Year: 2016 Type: Article Affiliation country: United States