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      Establishing Criteria for Human Mesenchymal Stem Cell Potency

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          Abstract

          This study sought to identify critical determinants of mesenchymal stem cell (MSC) potency using in vitro and in vivo attributes of cells isolated from the bone marrow of age‐ and sex‐matched donors. Adherence to plastic was not indicative of potency, yet capacity for long‐term expansion in vitro varied considerably between donors, allowing the grouping of MSCs from the donors into either those with high‐growth capacity or low‐growth capacity. Using this grouping strategy, high‐growth capacity MSCs were smaller in size, had greater colony‐forming efficiency, and had longer telomeres. Cell‐surface biomarker analysis revealed that the International Society for Cellular Therapy (ISCT) criteria did not distinguish between high‐growth capacity and low‐growth capacity MSCs, whereas STRO‐1 and platelet‐derived growth factor receptor alpha were preferentially expressed on high‐growth capacity MSCs. These cells also had the highest mean expression of the mRNA transcripts TWIST‐1 and DERMO‐1. Irrespective of these differences, both groups of donor MSCs produced similar levels of key growth factors and cytokines involved in tissue regeneration and were capable of multilineage differentiation. However, high‐growth capacity MSCs produced approximately double the volume of mineralized tissue compared to low‐growth capacity MSCs when assessed for ectopic bone‐forming ability. The additional phenotypic criteria presented in this study when combined with the existing ISCT minimum criteria and working proposal will permit an improved assessment of MSC potency and provide a basis for establishing the quality of MSCs prior to their therapeutic application. S tem C ells 2015;33:1878–1891

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          Mesenchymal stem cell therapy: Two steps forward, one step back.

          Mesenchymal stem cell (MSC) therapy is poised to establish a new clinical paradigm; however, recent trials have produced mixed results. Although MSC were originally considered to treat connective tissue defects, preclinical studies revealed potent immunomodulatory properties that prompted the use of MSC to treat numerous inflammatory conditions. Unfortunately, although clinical trials have met safety endpoints, efficacy has not been demonstrated. We believe the challenge to demonstrate efficacy can be attributed in part to an incomplete understanding of the fate of MSC following infusion. Here, we highlight the clinical status of MSC therapy and discuss the importance of cell-tracking techniques, which have advanced our understanding of the fate and function of systemically infused MSC and might improve clinical application. Copyright 2010 Elsevier Ltd. All rights reserved.
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            MSC-based product characterization for clinical trials: an FDA perspective.

            Proposals submitted to the FDA for MSC-based products are undergoing a rapid expansion that is characterized by increased variability in donor and tissue sources, manufacturing processes, proposed functional mechanisms, and characterization methods. Here we discuss the diversity in MSC-based clinical trial product proposals and highlight potential challenges for clinical translation. Copyright © 2014 Elsevier Inc. All rights reserved.
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              Expansion of human adult stem cells from bone marrow stroma: conditions that maximize the yields of early progenitors and evaluate their quality.

              There is considerable interest in the biology and therapeutic potential of adult stem cells from bone marrow stroma, variously referred to as mesenchymal stem cells or marrow stromal cells (MSCs). Human MSCs can expand rapidly in culture, but the rate of expansion and the yields of multipotential progenitors are inversely related to the plating density and incubation time of each passage. We have defined conditions for optimizing the yields of cultures enriched for early progenitors. Also, we developed a simple method for assessing the quality of the cultures by phase-contrast microscopy and image analysis or by forward light scatter in a flow cytometer. The cells expanded most rapidly on day 4 after plating, with a minimum average doubling time of about 10 hours for cells initially plated at 10 or 50 cells/cm(2). After plating the cells at 1 to 1000 cells/cm(2), the cultures underwent a time-dependent transition from early progenitors, defined as thin, spindle-shaped cells (RS-1A), to wider, spindle-shaped cells (RS-1B), and to still wider, spindle-shaped cells (RS-1C). Assays for adipogenesis demonstrated that the adipogenic potential of cultures was directly related to their ability to generate single-cell-derived colonies and their enrichment for RS-1A cells. In contrast, cultures enriched for RS-1B cells showed the greatest potential to differentiate into cartilage in a serum-free system. The results indicate that, when preparing cultures of human MSCs, it is necessary to compromise between conditions that provide the highest overall yields and those that provide the highest content of early progenitor cells.
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                Author and article information

                Journal
                Stem Cells
                Stem Cells
                10.1002/(ISSN)1549-4918
                STEM
                Stem Cells (Dayton, Ohio)
                John Wiley and Sons Inc. (Hoboken )
                1066-5099
                1549-4918
                June 2015
                21 May 2015
                : 33
                : 6 ( doiID: 10.1002/stem.v33.6 )
                : 1878-1891
                Affiliations
                [ 1 ]Glycotherapeutics Group
                [ 2 ] Advanced Wound Care LaboratoryInstitute of Medical Biology, A*STAR Singapore
                [ 3 ]Department of Biomedical Engineering
                [ 4 ]Department of Biochemistry
                [ 5 ]NUS Tissue Engineering Programme
                [ 6 ] Department of Orthopedic SurgeryNational University of Singapore Singapore
                [ 7 ] Department of Biological SciencesNational University of Singapore Singapore
                [ 8 ]Singapore Immunology Network (SIgN), A*STAR Singapore
                [ 9 ] Stem Cell and Regenerative BiologyGenome Institute of Singapore, A*STAR Singapore
                [ 10 ] School of Biological SciencesNanyang Technological University Singapore
                [ 11 ]Lee Kong Chian School of Medicine, Nanyang Technological University Singapore
                [ 12 ]Sciences, Singapore University of Technology and Design 8 Somapah Road Singapore
                Author notes
                [*] [* ]Correspondence: Simon M. Cool, Ph.D., 8A, Biomedical Grove, #06‐06 Immunos, Institute of Medical Biology, A*STAR, Singapore 138648. Telephone: 65‐6407‐0176; Fax: 65‐6478‐9477; e‐mail: simon.cool@ 123456imb.a-star.edu.sg
                Article
                STEM1982
                10.1002/stem.1982
                5363381
                25752682
                e2747243-7245-40f2-8a20-37c2a7d2cb56
                © 2015 The Authors STEM CELLS published by Wiley Periodicals, Inc. on behalf of AlphaMed Press

                This is an open access article under the terms of the Creative Commons Attribution License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.

                History
                : 03 December 2014
                : 08 January 2015
                Page count
                Pages: 14
                Funding
                Funded by: Singapore's Agency for Science, Technology, and Research (A*STAR)
                Funded by: Institute of Medical Biology (IMB)
                Funded by: National Medical Research Council (NMRC), Singapore
                Categories
                Translational and Clinical Research
                Translational and Clinical Research
                Custom metadata
                2.0
                stem1982
                June 2015
                Converter:WILEY_ML3GV2_TO_NLMPMC version:5.0.9 mode:remove_FC converted:23.03.2017

                Molecular medicine
                mesenchymal stem/stromal cells,quality,growth capacity,potency,stro‐1,pdgfr‐α
                Molecular medicine
                mesenchymal stem/stromal cells, quality, growth capacity, potency, stro‐1, pdgfr‐α

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