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Prospectively defined murine mesenchymal stem cells inhibit Klebsiella pneumoniae-induced acute lung injury and improve pneumonia survival

Hackstein, Holger ; Lippitsch, Anne ; Krug, Philipp ; Schevtschenko, Inna ; Kranz, Sabine ; Hecker, Matthias ; Dietert, Kristina ; Gruber, Achim D. ; Bein, Gregor ; Brendel, Cornelia ; Baal, Nelli


Originalveröffentlichung: (2015) Respiratory Research 16:1223 doi:10.1186/s12931-015-0288-1
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URN: urn:nbn:de:hebis:26-opus-121875
URL: http://geb.uni-giessen.de/geb/volltexte/2016/12187/


Freie Schlagwörter (Englisch): pneumonia , mesenchymal stem cells , Klebsiella pneumonia , acute lung injury
Sammlung: Open Access - Publikationsfonds
Universität Justus-Liebig-Universit√§t Gie√üen
Institut: Institute for Clinical Immunology and Transfusion Medicine
Fachgebiet: Medizin
DDC-Sachgruppe: Medizin
Dokumentart: Aufsatz
Sprache: Englisch
Erstellungsjahr: 2015
Publikationsdatum: 20.07.2016
Kurzfassung auf Englisch: Background: Numerous studies have described the immunosuppressive capacity of mesenchymal stem cells (MSC) but these studies use mixtures of heterogeneous progenitor cells for in vitro expansion. Recently, multipotent MSC have been prospectively identified in murine bone marrow (BM) on the basis of PDFGRa+ SCA1+ CD45- TER119- (PaS) expression but the immunomodulatory capacity of these MSC is unknown.
Methods: We isolated PaS MSC by high-purity FACS sorting of murine BM and after in vitro expansion we analyzed the in vivo immunomodulatory activity during acute pneumonia. PaS MSC (1?√ó?106) were applied intratracheally 4 h after acute respiratory Klebsiella pneumoniae induced infection.
Results: PaS MSC treatment resulted in significantly reduced alveolitis and protein leakage in comparison to mock-treated controls. PaS MSC-treated mice exhibited significantly reduced alveolar TNF-a and IL-12p70 expression, while IL-10 expression was unaffected. Dissection of respiratory dendritic cell (DC) subsets by multiparameter flow cytometry revealed significantly reduced lung DC infiltration and significantly reduced CD86 costimulatory expression on lung CD103+ DC in PaS MSC-treated mice. In the post-acute phase of pneumonia, PaS MSC-treated animals exhibited significantly reduced respiratory IL-17+ CD4+ T cells and IFN-gamma+ CD4+ T cells. Moreover, PaS MSC treatment significantly improved overall pneumonia survival and did not increase bacterial load.
Conclusion: In this study we demonstrated for the first time the feasibility and in vivo immunomodulatory capacity of prospectively defined MSC in pneumonia.
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