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Sökning: WFRF:(Jacobsen Sten Eirik W) > Potential risks of ...

Potential risks of bone marrow cell transplantation into infarcted hearts

Breitbach, Martin (författare)
University of Bonn, Bonn, Germany
Bostani, Toktam (författare)
University of Bonn, Bonn, Germany
Roell, Wilhelm (författare)
University of Bonn, Bonn, Germany
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Xia, Ying (författare)
University of Cologne, Cologne, Germany
Dewald, Oliver (författare)
University of Bonn, Bonn, Germany
Nygren, Jens Martin, 1976- (författare)
Lund University,Lunds universitet,Medicinska fakulteten,Faculty of Medicine,Lund Strategic Research Center for Stem Cell Biology and Cell Therapy, Lund University, Lund, Sweden
Fries, Jochen W. U. (författare)
University of Cologne, Cologne, Germany
Tiemann, Klaus (författare)
University of Bonn, Bonn, Germany
Bohlen, Heribert (författare)
Axiogenesis AG, Cologne, Germany
Hescheler, Juergen (författare)
University of Cologne, Cologne, Germany
Welz, Armin (författare)
University of Bonn, Bonn, Germany
Bloch, Wilhelm (författare)
German Sport University, Cologne, Germany
Jacobsen, Sten Eirik W (författare)
Lund University,Lunds universitet,Stamcellscentrum (SCC),Avdelningen för stamcellsforskning,Institutionen för laboratoriemedicin,Medicinska fakulteten,Stem Cell Center,Division of stem cell research,Department of Laboratory Medicine,Faculty of Medicine,Lund Strategic Research Center for Stem Cell Biology and Cell Therapy, Lund University, Lund, Sweden
Fleischmann, Bernd K (författare)
University of Bonn, Bonn, Germany
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 (creator_code:org_t)
Washington, DC : American Society of Hematology, 2007
2007
Engelska.
Ingår i: Blood. - Washington, DC : American Society of Hematology. - 0006-4971 .- 1528-0020. ; 110:4, s. 1362-1369
  • Tidskriftsartikel (refereegranskat)
Abstract Ämnesord
Stäng  
  • Cellular replacement therapy has emerged as a novel strategy for the treatment of heart failure. The aim of our study was to determine the fate of injected mesenchymal stem cells (MSCs) and whole bone marrow (BM) cells in the infarcted heart. MSCs were purified from BM of transgenic mice and characterized using flow cytometry and in vitro differentiation assays. Myocardial infarctions were generated in mice and different cell populations including transgenic MSCs, unfractionated BM cells, or purified hematopoietic progenitors were injected. Encapsulated structures were found in the infarcted areas of a large fraction of hearts after injecting MSCs (22 of 43, 51.2%) and unfractionated BM cells (6 of 46, 13.0%). These formations contained calcifications and/or ossifications. In contrast, no pathological abnormalities were found after injection of purified hematopoietic progenitors (0 of 5, 0.0%), fibroblasts (0 of 5, 0.0%), vehicle only (0 of 30, 0.0%), or cytokine-induced mobilization of BM cells (0 of 35, 0.0%). We conclude that the developmental fate of BM-derived cells is not restricted by the surrounding tissue after myocardial infarction and that the MSC fraction underlies the extended bone formation in the infarcted myocardium. These findings seriously question the biologic basis and clinical safety of using whole BM and in particular MSCs to treat nonhematopoietic disorders.

Ämnesord

MEDICIN OCH HÄLSOVETENSKAP  -- Klinisk medicin -- Hematologi (hsv//swe)
MEDICAL AND HEALTH SCIENCES  -- Clinical Medicine -- Hematology (hsv//eng)

Nyckelord

Animals
Bone marrow transplantation
Cell differentiation
Cultured cells
Flow cytometry
Green fluorescent proteins
Mesenchymal stem cell transplantation
Mice
Inbred C57BL mice
Transgenic mice
Myocardial infarction
Risk factors
Treatment outcome
MEDICINE
MEDICIN

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