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Sci Rep ; 5: 16570, 2015 Nov 13.
Article in English | MEDLINE | ID: mdl-26564250

ABSTRACT

Due to their immunosuppressive properties, mesenchymal stem cells (MSC) have been evaluated for the treatment of immunological diseases. However, the animal-derived growth supplements utilized for MSC manufacturing may lead to clinical complications. Characterization of alternative media formulations is imperative for MSC therapeutic application. Human BMMSC and AdMSC were expanded in media supplemented with either human platelet lysates (HPL), serum-free media/xeno-free FDA-approved culture medium (SFM/XF), or fetal bovine serum (FBS) and the effects on their properties were investigated. The immunophenotype of resting and IFN-γ primed BMMSC and AdMSC remained unaltered in all media. Both HPL and SFM/XF increased the proliferation of BMMSC and AdMSC. Expansion of BMMSC and AdMSC in HPL increased their differentiation, compared to SFM/XF and FBS. Resting BMMSC and AdMSC, expanded in FBS or SFM/XF, demonstrated potent immunosuppressive properties in both non-primed and IFN-γ primed conditions, whereas HPL-expanded MSC exhibited diminished immunosuppressive properties. Finally, IFN-γ primed BMMSC and AdMSC expanded in SFM/XF and HPL expressed attenuated levels of IDO-1 compared to FBS. Herein, we provide strong evidence supporting the use of the FDA-approved SFM/XF medium, in contrast to the HPL medium, for the expansion of MSC towards therapeutic applications.


Subject(s)
Cell Differentiation/drug effects , Cell Proliferation/drug effects , Culture Media/pharmacology , Mesenchymal Stem Cells/drug effects , Adipogenesis/drug effects , Adipogenesis/genetics , Adiponectin/genetics , Alkaline Phosphatase/genetics , Animals , Blood Platelets/chemistry , Cattle , Cell Culture Techniques/methods , Cell Differentiation/genetics , Cell Extracts/pharmacology , Cell Proliferation/genetics , Culture Media/chemistry , Culture Media, Serum-Free/pharmacology , Fetal Blood/chemistry , Gene Expression/drug effects , Humans , Immunoblotting , Indoleamine-Pyrrole 2,3,-Dioxygenase/metabolism , Interferon-gamma/pharmacology , Mesenchymal Stem Cells/cytology , Mesenchymal Stem Cells/metabolism , Osteogenesis/drug effects , Osteogenesis/genetics , PPAR gamma/genetics , Reverse Transcriptase Polymerase Chain Reaction , Serum/chemistry
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