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ABSTRACT: Background
Clinical translation of mesenchymal stromal cells (MSCs) necessitates basic characterization of the cell product since variability in biological source and processing of MSCs may impact therapeutic outcomes. Although expression of classical cell surface markers (e.g., CD90, CD73, CD105, and CD44) is used to define MSCs, identification of functionally relevant cell surface markers would provide more robust release criteria and options for quality control. In addition, cell surface expression may distinguish between MSCs from different sources, including bone marrow-derived MSCs and clinical-grade adipose-derived MSCs (AMSCs) grown in human platelet lysate (hPL).Methods
In this work we utilized quantitative PCR, flow cytometry, and RNA-sequencing to characterize AM
SUBMITTER: Camilleri ET
PROVIDER: S-EPMC4982273 | biostudies-literature | 2016 Aug
REPOSITORIES: biostudies-literature