Literature DB >> 17889212

Umbilical cord blood-derived stem cells spontaneously express cardiomyogenic traits.

C Prat-Vidal1, S Roura, J Farré, C Gálvez, A Llach, C E Molina, L Hove-Madsen, J Garcia, J Cinca, A Bayes-Genis.   

Abstract

BACKGROUND: Umbilical cord blood (UCB) has been widely used for hematopoietic stem cell transplantation. The UCB-derived stem cells (UCBSCs) have been proposed as an alternative to bone marrow (BM)-derived mesenchymal stem cells (MSCs) for cardiac cell-based therapy. Herein we studied whether UCBSCs spontaneously exhibit cardiac-specific markers in vitro.
METHODS: Human UCBSCs were isolated, expanded, and phenotyped by flow cytometry, quantitative RT-PCR, and immunofluorescence. Cell pluripotency and proliferation were also assessed by adipogenic and osteogenic media and in growth assays.
RESULTS: Among 25 analyzed UCB, 16% of cases afforded primary culture satisfactory generation of UCBSCs. Duplication time (Td) of cultures was 2.16 +/- 0.06 days. The cells were strongly positive for CD105 (18.5 +/- 0.14), CD44 (27 +/- 2.8), CD166 (13 +/- 9), CD29 (59 +/- 9.4), CD90 (60 +/- 11) and consistently negative for CD117 (1.2 +/- 0.1), CD106 (1.1 +/- 0), CD34 (1.2 +/- 0.2), CD14 (1 +/- 0), and CD45 (1 +/- 0), consistent with a mesenchymal lineage. Adipogenesis and osteogenesis of cells resulted in low accumulation of intracellular lipid droplets and high deposition of calcium. The UCBSCs showed gene transcripts for alpha-actinin, connexin (Cx)-43, SERCA-2, and stromal cell-derived factor (SDF)-1alpha. At the protein level, the cells abundantly expressed alpha-actinin, Cx-43, SERCA-2 and SDF-1alpha. In contrast, these cells did not express the cardiac transcription factors GATA-4, Tbx5, and Nkx2.5, nor the sarcomeric proteins beta-myosin heavy chain (beta-MyHC) or cardiac troponin I (cTnI).
CONCLUSIONS: Human UCBSCs may represent an alternative source of stem cells for myocardial-cell replacement. These cells can be highly expanded. They spontaneously express proteins of paramount importance for cardiovascular regeneration, such as Cx-43, SERCA-2, and SDF-1alpha.

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Year:  2007        PMID: 17889212     DOI: 10.1016/j.transproceed.2007.06.016

Source DB:  PubMed          Journal:  Transplant Proc        ISSN: 0041-1345            Impact factor:   1.066


  14 in total

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3.  Postinfarction Functional Recovery Driven by a Three-Dimensional Engineered Fibrin Patch Composed of Human Umbilical Cord Blood-Derived Mesenchymal Stem Cells.

Authors:  Santiago Roura; Carolina Soler-Botija; Juli R Bagó; Aida Llucià-Valldeperas; Marco A Férnandez; Carolina Gálvez-Montón; Cristina Prat-Vidal; Isaac Perea-Gil; Jerónimo Blanco; Antoni Bayes-Genis
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6.  Human umbilical cord blood-derived mesenchymal stem cells promote vascular growth in vivo.

Authors:  Santiago Roura; Juli R Bagó; Carolina Soler-Botija; Josep M Pujal; Carolina Gálvez-Montón; Cristina Prat-Vidal; Aida Llucià-Valldeperas; Jerónimo Blanco; Antoni Bayes-Genis
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7.  Preclinical evaluation of the immunomodulatory properties of cardiac adipose tissue progenitor cells using umbilical cord blood mesenchymal stem cells: a direct comparative study.

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Review 9.  The role and potential of umbilical cord blood in an era of new therapies: a review.

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10.  Direct contact of umbilical cord blood endothelial progenitors with living cardiac tissue is a requirement for vascular tube-like structures formation.

Authors:  Marilena Lupu; Markus Khalil; Florin Iordache; Eugen Andrei; Kurt Pfannkuche; Dimitry Spitkovsky; Sven Baumgartner; Martin Rubach; Heba Abdelrazik; Cosmin Buzila; Konrad Brockmeier; Maya Simionescu; Jürgen Hescheler; Horia Maniu
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