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dc.creatorLuth, E. S.en
dc.creatorJun, S. J.en
dc.creatorWessen, M. K.en
dc.creatorLiadaki, K.en
dc.creatorGussoni, E.en
dc.creatorKunkel, L. M.en
dc.date.accessioned2015-11-23T10:38:14Z
dc.date.available2015-11-23T10:38:14Z
dc.date.issued2008
dc.identifier10.1242/jcs.021675
dc.identifier.issn219533
dc.identifier.urihttp://hdl.handle.net/11615/30440
dc.description.abstractAlthough the contribution of bone marrow-derived cells to regenerating skeletal muscle has been repeatedly documented, there remains considerable debate as to whether this incorporation is exclusively a result of inflammatory cell fusion to regenerating myofibers or whether certain populations of bone marrow-derived cells have the capacity to differentiate into muscle. The present study uses a dual-marker approach in which GFP+ cells were intravenously transplanted into lethally irradiated β-galactosidase+ recipients to allow for simple determination of donor and host contribution to the muscle. FACS analysis of cardiotoxin-damaged muscle revealed that CD45+ bone-marrow side-population (SP) cells, a group enriched in hematopoietic stem cells, can give rise to CD45-/Sca1+/desmin+ cells capable of myogenic differentiation. Moreover, after immunohistochemical examination of the muscles of both SP- and whole bone marrow-transplanted animals, we noted the presence of myofibers composed only of bone marrow-derived cells. Our findings suggest that a subpopulation of bone marrow SP cells contains precursor cells whose progeny have the potential to differentiate towards a muscle lineage and are capable of de novo myogenesis following transplantation and initiation of muscle repair via chemical damage.en
dc.source.urihttp://www.scopus.com/inward/record.url?eid=2-s2.0-46649095842&partnerID=40&md5=d18c004eb76c11c1f7269eaba897a1a4
dc.subjectBone marrowen
dc.subjectProgenitoren
dc.subjectSide populationen
dc.subjectSkeletal muscleen
dc.subjectataxin 1en
dc.subjectbeta galactosidaseen
dc.subjectcardiotoxinen
dc.subjectCD45 antigenen
dc.subjectdesminen
dc.subjectMyoD proteinen
dc.subjecttranscription factor PAX7en
dc.subjectanimal cellen
dc.subjectanimal tissueen
dc.subjectarticleen
dc.subjectbone marrow cellen
dc.subjectbone marrow transplantationen
dc.subjectcell differentiationen
dc.subjectcell lineageen
dc.subjectcell populationen
dc.subjectcontrolled studyen
dc.subjectfemaleen
dc.subjectfluorescence activated cell sortingen
dc.subjecthematopoietic stem cellen
dc.subjectimmunohistochemistryen
dc.subjectmaleen
dc.subjectmouseen
dc.subjectmuscle developmenten
dc.subjectmuscle fibrilen
dc.subjectmuscle injuryen
dc.subjectmuscle regenerationen
dc.subjectnonhumanen
dc.subjectpriority journalen
dc.subjectstem cellen
dc.subjectAnimalsen
dc.subjectAntigens, CD45en
dc.subjectbeta-Galactosidaseen
dc.subjectBiological Markersen
dc.subjectBone Marrow Cellsen
dc.subjectCell Counten
dc.subjectCell Separationen
dc.subjectGreen Fluorescent Proteinsen
dc.subjectMiceen
dc.subjectMuscle Fibersen
dc.subjectNerve Tissue Proteinsen
dc.subjectNuclear Proteinsen
dc.subjectRegenerationen
dc.subjectStem Cellsen
dc.subjectAnimaliaen
dc.titleBone marrow side population cells are enriched for progenitors capable of myogenic differentiationen
dc.typejournalArticleen


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