comparison of epithelial differentiation and immune regulatory properties of mesenchymal stromal cells derived from human lung and bone marrow比较上皮间充质基质细胞的分化和免疫监管性质来源于人类的肺和骨髓.pdfVIP

comparison of epithelial differentiation and immune regulatory properties of mesenchymal stromal cells derived from human lung and bone marrow比较上皮间充质基质细胞的分化和免疫监管性质来源于人类的肺和骨髓.pdf

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comparison of epithelial differentiation and immune regulatory properties of mesenchymal stromal cells derived from human lung and bone marrow比较上皮间充质基质细胞的分化和免疫监管性质来源于人类的肺和骨髓

Comparison of Epithelial Differentiation and Immune Regulatory Properties of Mesenchymal Stromal Cells Derived from Human Lung and Bone Marrow 1 2 1 1 1 ´ Mario Ricciardi , Giorgio Malpeli , Francesco Bifari , Giulio Bassi , Luciano Pacelli , Armel Herve 1 2 1 Nwabo Kamdje , Marco Chilosi , Mauro Krampera * 1 Stem Cell Research Laboratory, Section of Hematology, Department of Medicine, University of Verona, Verona, Italy, 2 Section of Pathological Anatomy, Department of Pathology and Diagnostics, University of Verona, Verona, Italy Abstract Mesenchymal stromal cells (MSCs) reside in many organs including lung, as shown by their isolation from fetal lung tissues, bronchial stromal compartment, bronchial-alveolar lavage and transplanted lung tissues. It is still controversial whether lung MSCs can undergo mesenchymal-to-epithelial-transition (MET) and possess immune regulatory properties. To this aim, we isolated, expanded and characterized MSCs from normal adult human lung (lung-hMSCs) and compared with human bone marrow-derived MSCs (BM-hMSCs). Our results show that lung-MSCs reside at the perivascular level and do not significantly differ from BM-hMSCs in terms of immunophenotype, stemness gene profile, mesodermal differentiation potential and modulation of T, B and NK cells. However, lung-hMSCs express higher basal level of the stemness-related marker nestin and show, following in vitro treatment with retinoic acid, higher epithelial cell polarization, which is anyway partial when compared to a control epithelial bronchial cell line. Although these results question the real capability of acquiring epithelial functions by MSCs and the feas

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