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Prolonged Survival and expression of neural markers by bone marrow-derived stem cells transplanted into brain lesions
Department of Neurobiology, International Center of Neurological Restoration, CIREN, Havana, Cuba..
Interfaculty Institute for Biochemistry, University of Tübingen, Germany; BioApplications Enterprises, Winnipeg, MB, Canada.
Department of Neurobiology, International Center of Neurological Restoration, CIREN, Havana, Cuba..
Department of Neurobiology, International Center of Neurological Restoration, CIREN, Havana, Cuba..
Vise andre og tillknytning
2009 (engelsk)Inngår i: Medical Science Monitor, ISSN 1234-1010, E-ISSN 1643-3750, Vol. 15, nr 2, s. BR47-BR54Artikkel i tidsskrift (Fagfellevurdert) Published
Abstract [en]

BACKGROUND: Bone marrow-derived stem cell transplantation is a potentially viable therapeutic option for the treatment of neurodegenerative disease. MATERIAL/METHODS: We have isolated bone marrow stem cells by standard method. We then evaluated the survival of rats' bone marrow mononuclear cells implanted in rats' brain. The cells were extracted from rats' femurs, and marked for monitoring purposes by adenoviral transduction with Green Fluorescent Protein (GFP). Labeled cells were implanted within the area of rats' striatum lesions that were induced a month earlier employing quinolinic acid-based method. The implants were phenotyped by monitoring CD34; CD38; CD45 and CD90 expression. Bone marrow stromal cells were extracted from rats' femurs and cultivated until monolayer bone marrow stromal cells were obtained. The ability of bone marrow stromal cells to express NGF and GDNF was evaluated by RT-PCR. RESULTS: Implanted cells survived for at least one month after transplantation and dispersed from the area of injection towards corpus callosum and brain cortex. Interestingly, passaged rat bone marrow stromal cells expressed NGF and GDNF mRNA. CONCLUSIONS: The bone marrow cells could be successfully transplanted to the brain either for the purpose of trans-differentiation, or for the expression of desired growth factors.

sted, utgiver, år, opplag, sider
2009. Vol. 15, nr 2, s. BR47-BR54
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URN: urn:nbn:se:liu:diva-86916ISI: 000264300800005OAI: oai:DiVA.org:liu-86916DiVA, id: diva2:583184
Tilgjengelig fra: 2013-01-07 Laget: 2013-01-07 Sist oppdatert: 2017-12-06

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