Document Detail


Stem cells used for cardiovascular tissue engineering.
MedLine Citation:
PMID:  18468449     Owner:  NLM     Status:  MEDLINE    
Abstract/OtherAbstract:
Stem cell research and tissue engineering have become leading fields in basic research worldwide. Especially in cardiovascular medicine, initial reports on the potential of using stem cells to recover cardiac function and replace organ subunits such as heart valves seemed to offer the promise of widespread clinical use in the near future. However, the broad application of this new therapy failed due to safety and efficacy concerns. Due in part to the initial reports, major basic research efforts were undertaken to explore the specific cell types in greater detail and identify their mechanisms of supporting function, resulting in remarkable new findings in stem cell biology. For example, the notion of resident human cardiac stem cells has disproved the earlier supposition that the human heart is a finitely differentiated organ without the intrinsic potential for regeneration. Furthermore, new technologies emerged to produce pluripotent cells without the ethical and immunological drawbacks of embryonic stem cells (for instance by nuclear transfer). Other autologous cell sources are presently under investigation in myocardial tissue engineering. For tissue engineering of heart valves and small calibre vessels, the use of autologous endothelial (precursor) cells may be the optimal means of seeding a biological or artificial scaffold. It is important that ongoing basic and clinical research in cardiovascular surgery might explore the potential of different cell types either using tissue engineering constructs or in cell transplantation approaches.
Authors:
Matthias Siepe; Payam Akhyari; Artur Lichtenberg; Christian Schlensak; Friedhelm Beyersdorf
Related Documents :
24910429 - Acquired dependence of acute myeloid leukemia on the dead-box rna helicase ddx5.
23060879 - Novel microchip-based tools facilitating live cell imaging and assessment of functional...
23278749 - The establishment of the plasma cell survival niche in the bone marrow.
23820889 - Cd8+ t cell granzyme b activates keratinocyte endogenous il-18.
23552359 - Granulomatous inflammation in acanthamoeba sclerokeratitis.
25007029 - Upregulated interleukin-21 receptor on b cells associated with the downregulation of ig...
10611899 - Bone marrow: target for gene transfer.
2962929 - T lymphocytes emigrating from the thymus to the spleen during postpartum regulate serum...
11973649 - Differential regulation of the response to dna damage in ewing's sarcoma cells by ets1 ...
Publication Detail:
Type:  Journal Article; Review     Date:  2008-05-08
Journal Detail:
Title:  European journal of cardio-thoracic surgery : official journal of the European Association for Cardio-thoracic Surgery     Volume:  34     ISSN:  1010-7940     ISO Abbreviation:  Eur J Cardiothorac Surg     Publication Date:  2008 Aug 
Date Detail:
Created Date:  2008-07-14     Completed Date:  2009-03-03     Revised Date:  -    
Medline Journal Info:
Nlm Unique ID:  8804069     Medline TA:  Eur J Cardiothorac Surg     Country:  Germany    
Other Details:
Languages:  eng     Pagination:  242-7     Citation Subset:  IM    
Affiliation:
Department of Cardiovascular Surgery, University Clinic Freiburg, Hugstetterstrasse 55, Freiburg, Germany. matthias.siepe@web.de
Export Citation:
APA/MLA Format     Download EndNote     Download BibTex
MeSH Terms
Descriptor/Qualifier:
Bioartificial Organs
Blood Vessel Prosthesis*
Endothelium, Vascular / cytology
Heart Valve Prosthesis*
Heart Valve Prosthesis Implantation / methods
Humans
Regeneration
Stem Cell Transplantation / methods
Tissue Engineering / methods*
Comments/Corrections
Comment In:
Eur J Cardiothorac Surg. 2008 Aug;34(2):227-8   [PMID:  18585049 ]

From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine


Previous Document:  Late reoperations after neonatal arterial switch operation for transposition of the great arteries.
Next Document:  A theoretical study on the quenching mechanisms of triplet state riboflavin by tryptophan and tyrosi...