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Antiapoptotic effect of implanted embryonic stem cell-derived early-differentiated cells in aging rats after myocardial infarction.

Antiapoptotic effect of implanted embryonic stem cell-derived early-differentiated cells in aging rats after myocardial infarction. Research Abstract Details 

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  • Antiapoptotic effect of implanted embryonic stem cell-derived early-differentiated cells in aging rats after myocardial infarction. Abstract Text:

    meixiang xiangMeixiang Xiang,jianan wangJianan Wang,emel kaplanEmel Kaplan,peter oettgenPeter Oettgen,lewis lipsitzLewis Lipsitz,james p morganJames P Morgan,jiang-yong minJiang-Yong Min,meixiang xiangMeixiang Xiang,jianan wangJianan Wang,emel kaplanEmel Kaplan,peter oettgenPeter Oettgen,lewis lipsitzLewis Lipsitz,james p morganJames P Morgan,jiang-yong minJiang-Yong Min,

    This study tested whether implanted embryonic stem cell-derived early-differentiated cells (EDCs) lead to improvement in cardiac function by preventing cardiac apoptosis in aging rats after myocardial infarction. Cardiac apoptosis after transplantation of EDCs was assessed in situ by terminal deoxynucleotidyl transferase-mediated dUTP-biotin nick end-labeling reaction (TUNEL) staining as well as by measurements of protein levels of cleaved caspases 3, Bax, and Bcl-2. Our results indicate that cell transplantation improved cardiac function at 6-months observation. The frequency of apoptotic cells in the peri-infarcted myocardium 3 days after cell transplantation was significantly decreased in the cell transplantation group. EDC therapy decreased the protein levels of cleaved caspase 3 and Bax, and increased the level of Bcl-2 in comparison to myocardial infarction control. Additionally, the number of apoptotic cells decreased significantly in cardiomyocytes precocultured with EDCs. This study demonstrates that functional improvement of EDC transplantation may at least in part be related to a reduction in cardiomyocyte apoptosis.

    Antiapoptotic effect of implanted embryonic stem cell-derived early-differentiated cells in aging rats after myocardial infarction. Publishing Authors By Initials

    m xiangM Xiang,j wangJ Wang,e kaplanE Kaplan,p oettgenP Oettgen,l lipsitzL Lipsitz,jp morganJP Morgan,jy minJY Min,m xiangM Xiang,j wangJ Wang,e kaplanE Kaplan,p oettgenP Oettgen,l lipsitzL Lipsitz,jp morganJP Morgan,jy minJY Min,

    For similar animals: animal population groups: animals, inbred strains: rats, inbred strains: rats, inbred f344 research abstracts see: animals: animal population groups: animals, inbred strains: rats, inbred strains: rats, inbred f344 research

    PUBMED ID PMID:

    MEDLINE DATE:

    Antiapoptotic effect of implanted embryonic stem cell-derived early-differentiated cells in aging rats after myocardial infarction. Journal Published:

    PUBLICATION TYPE: Research Support, Non-U.S. Gov

    Journal: The journals of gerontology. Series A, Biological

    VOLUME: 61

    Page Numbers: 1219-27

    Journal Abbreviation: J. Gerontol. A Biol. Sci. Med.

    ISSN: 1079-5006

    DAY: 3

    MONTH: Dec

    YEAR: 2006

    Antiapoptotic effect of implanted embryonic stem cell-derived early-differentiated cells in aging rats after myocardial infarction. Information

    Number of References:

    LANGUAGE: eng

    NlmUniqueID: 9502837

    Antiapoptotic effect of implanted embryonic stem cell-derived early-differentiated cells in aging rats after myocardial infarction. Keywords Mesh Terms:

    KEYWORDS: Rats, Inbred F344

    MESH TERMS: therapy

    Chemical & Substance for Abstract: Antiapoptotic effect of implanted embryonic stem cell-derived early-differentiated cells in aging rats after myocardial infarction. Information

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    Grant and Affiliation Information for Antiapoptotic effect of implanted embryonic stem cell-derived early-differentiated cells in aging rats after myocardial infarction.

    AFFILIATION: The 2nd Affiliated Hospital, Medical College of Zhejiang University, Hangzhou, China.

    Country: United States

    United States Research PublicationUnited States Research Publication

    AGENCY: United States NIA

    GRANT: 5P60 AG08812-13

    ACRONYM: AG

    MEDLINETA: J Gerontol A Biol Sci Med Sci

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