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Characterization of Mesenchymal Stromal Cells for Musculoskeletal Disorders and Regenerative Medicine

dc.contributor.advisorBurger, Christof
dc.contributor.authorHaddouti, El Mustapha
dc.date.accessioned2021-05-31T15:12:13Z
dc.date.available2021-05-31T15:12:13Z
dc.date.issued31.05.2021
dc.identifier.urihttps://hdl.handle.net/20.500.11811/9111
dc.description.abstractRecently, mesenchymal stromal cells (MSC) have come increasingly into focus as a therapeutic option for bone pathologies and regenerative medicine. While human MSCs have been extensively characterized and standardized, ovine MSCs are poorly understood. The current study reports a direct systematic comparison of human and ovine MSCs from three corresponding sources under the same conditions. All MSCs showed solid growth behavior and potent immunomodulatory capacity. In addition, common positive and negative surface markers were identified. Both human and ovine MSCs showed strong osteogenic potential.
Furthermore, the aim of this study was to isolate and characterize MSCs from the vertebral body of healthy non-osteoporotic and osteoporotic patients as the role of MSCs in osteoporosis is not fully understood. Isolated MSCs were characterized by their trilineage differentiation, surface marker expression, proliferation behavior, and immunomodulatory capacity. MSCs from both healthy and osteoporotic patients showed common morphology, proliferation behavior, expressed the typical MSC surface markers and possessed immunomodulatory capacity. Both groups demonstrated solid trilineage differentiation potential; osteogenic differentiation was further assessed by additional read outs such as optical density (OD) and free phosphate ion release.
Moreover, MSCs harvested from different tissues of the same donor have been shown to exhibit different phenotypes characterized by different cellular functionalities. In this study, we investigated the proteomic and functional properties of human bone marrow-derived MSCs (hBM-MSC) harvested either as aspirate or bone chip. Both MSC populations were profiled according to MSC markers defined by the International Society for Cellular Therapy (ISCT). hBM-MSCs derived from aspirate cultures demonstrated significantly higher osteogenic differentiation potential than MSCs grown from bone chip.
The key findings shown of this report reveal the utility of ovine MSCs in preclinical studies for MSC-based therapies. Furthermore, MSCs derived from vertebral body of osteoporotic patients were not impaired and possessed full osteogenic potential compared with MSCs from non-osteoporotic patients. Moreover, different harvesting techniques indicate the need for future standardized harvesting, processing, and phenotyping procedures to achieve better comparability in the MSC field.
en
dc.language.isoeng
dc.rightsIn Copyright
dc.rights.urihttp://rightsstatements.org/vocab/InC/1.0/
dc.subjectMesenchymale Stromazellen
dc.subjectOsteoporose
dc.subjectDifferenzierung
dc.subjectOberflächenmarker
dc.subjectRegenerative Medizin
dc.subjectCharakterisierung
dc.subjectPhenotypisierung
dc.subjectmesenchymal stromal cells
dc.subjectovine animal model
dc.subjectosteoporosis
dc.subjectregenerative medicine
dc.subjectimmunomodulation
dc.subjectdifferentiation
dc.subjectsurface markers
dc.subjectorthopedics
dc.subjectharvesting technique
dc.subjectphenotype
dc.subjectcharacterization
dc.subject.ddc610 Medizin, Gesundheit
dc.titleCharacterization of Mesenchymal Stromal Cells for Musculoskeletal Disorders and Regenerative Medicine
dc.typeDissertation oder Habilitation
dc.publisher.nameUniversitäts- und Landesbibliothek Bonn
dc.publisher.locationBonn
dc.rights.accessRightsopenAccess
dc.identifier.urnhttps://nbn-resolving.org/urn:nbn:de:hbz:5-62512
dc.relation.doihttps://doi.org/10.3390/ijms21072310
dc.relation.doihttps://doi.org/10.3390/ijms21218309
dc.relation.doihttps://doi.org/10.3390/ijms21124382
ulbbn.pubtypeErstveröffentlichung
ulbbnediss.affiliation.nameRheinische Friedrich-Wilhelms-Universität Bonn
ulbbnediss.affiliation.locationBonn
ulbbnediss.thesis.levelDissertation
ulbbnediss.dissID6251
ulbbnediss.date.accepted19.05.2021
ulbbnediss.instituteMedizinische Fakultät / Kliniken : Klinik und Poliklinik für Orthopädie und Unfallchirurgie
ulbbnediss.fakultaetMedizinische Fakultät
dc.contributor.coRefereeStoddart, Martin
ulbbnediss.contributor.gnd1227782667


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