Literature DB >> 23400434

Isolation of muscle-derived stem/progenitor cells based on adhesion characteristics to collagen-coated surfaces.

Mitra Lavasani1, Aiping Lu, Seth D Thompson, Paul D Robbins, Johnny Huard, Laura J Niedernhofer.   

Abstract

Our lab developed and optimized a method, known as the modified pre-plate technique, to isolate stem/progenitor cells from skeletal muscle. This method separates different populations of myogenic cells based on their propensity to adhere to a collagen I-coated surface. Based on their surface markers and stem-like properties, including self-renewal, multi-lineage differentiation, and ability to promote tissue regeneration, the last cell fraction or slowest to adhere to the collagen-coated surface (pre-plate 6; pp6) appears to be early, quiescent progenitor cells termed muscle-derived stem/progenitor cells (MDSPCs). The cell fractions preceding pp6 (pp1-5) are likely populations of more committed (differentiated) cells, including fibroblast- and myoblast-like cells. This technique may be used to isolate MDSPCs from skeletal muscle of humans or mice regardless of age, sex or disease state, although the yield of MDSPCs varies with age and health. MDSPCs can be used for regeneration of a variety of tissues including bone, articular cartilage, skeletal and cardiac muscle, and nerve. MDSPCs are currently being tested in clinical trials for treatment of urinary incontinence and myocardial infarction. MDSPCs from young mice have also been demonstrated to extend life span and healthspan in mouse models of accelerated aging through an apparent paracrine/endocrine mechanism. Here we detail methods for isolation and characterization of MDSPCs.

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Year:  2013        PMID: 23400434      PMCID: PMC3731996          DOI: 10.1007/978-1-62703-317-6_5

Source DB:  PubMed          Journal:  Methods Mol Biol        ISSN: 1064-3745


  61 in total

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4.  Hematopoietic potential of stem cells isolated from murine skeletal muscle.

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Authors:  J Y Lee; D Musgrave; D Pelinkovic; K Fukushima; J Cummins; A Usas; P Robbins; F H Fu; J Huard
Journal:  J Bone Joint Surg Am       Date:  2001-07       Impact factor: 5.284

Review 6.  Gene therapy strategies for urological dysfunction.

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8.  Human skeletal muscle cells in ex vivo gene therapy to deliver bone morphogenetic protein-2.

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Journal:  Urology       Date:  2003-11       Impact factor: 2.649

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  36 in total

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3.  Activation of non-myogenic mesenchymal stem cells during the disease progression in dystrophic dystrophin/utrophin knockout mice.

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Journal:  Hum Mol Genet       Date:  2015-04-09       Impact factor: 6.150

Review 4.  Extracellular vesicles and aging.

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5.  Rapid depletion of muscle progenitor cells in dystrophic mdx/utrophin-/- mice.

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7.  Muscle metabolic reprogramming underlies the resistance of liver fatty acid-binding protein (LFABP)-null mice to high-fat feeding-induced decline in exercise capacity.

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8.  Discussion: Regeneration of Vascularized Corticocancellous Bone and Diploic Space Using Muscle-Derived Stem Cells: A Translational Biologic Alternative for Healing Critical Bone Defects.

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Review 9.  Stem cells for skeletal muscle regeneration: therapeutic potential and roadblocks.

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10.  A Pitx2-MicroRNA Pathway Modulates Cell Proliferation in Myoblasts and Skeletal-Muscle Satellite Cells and Promotes Their Commitment to a Myogenic Cell Fate.

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