Induced Pluripotent Stem (iPS) Cells Repair and Regenerate Infarcted Myocardium

    Authors

    D. K. Singla; X. L. Long; C. Glass; R. D. Singla;B. B. Yan

    Comments

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    Abbreviated Journal Title

    Mol. Pharm.

    Keywords

    induced pluripotent stem cells; apoptosis; fibrosis and regenerate; INHIBIT APOPTOSIS; CARDIAC PROTECTION; HUMAN BLASTOCYSTS; H9C2 CELLS; RAT-HEART; DIFFERENTIATION; TRANSPLANTATION; CARDIOMYOCYTES; LINEAGES; PATHWAY; Medicine, Research & Experimental; Pharmacology & Pharmacy

    Abstract

    Cardiac myocyte differentiation reported thus far is A from iPS cells generated from mouse and human fibroblasts. However, there is no article on the generation of iPS cells from cardiac ventricular specific cell types such as H9c2 cells. Therefore, whether transduced H9c2 cells, originally isolated from embryonic cardiac ventricular tissue, will be able to generate iPS cells and have the potential to repair and regenerate infarcted myocardium remains completely elusive. We transduced H9c2 cells with four sternness factors, Oct3/4, Sox2, Klf4, and c-Myc, and successfully reprogrammed them into iPS cells. These if'S cells were able to differentiate into beating cardiac myocytes and positively stained for cardiac specific sarcomeric a-actin and myosin heavy chain proteins. Following transplantation in the infarcted myocardium, there were newly differentiated cardiac myocytes and formation of gap junction proteins at 2 weeks post-myocardial infarction (MO, suggesting newly formed cardiac myocytes were integrated into the native myocardium. Furthermore, transplanted iPS cells significantly (p < 0.05) inhibited apoptosis and fibrosis and improved cardiac function compared with MI and MI+H9c2 cell groups. Moreover, our iPS cell derived cardiac myocyte differentiation in vitro and in vivo was comparable to embryonic stem cells in the present study. In conclusion we report for the first time that we have H9c2 cell-derived IFS cells which contain the potential to differentiate into cardiac myocytes in the cell culture system and repair and regenerate infarcted myocardium with improved cardiac function in vivo.

    Journal Title

    Molecular Pharmaceutics

    Volume

    8

    Issue/Number

    5

    Publication Date

    1-1-2011

    Document Type

    Article

    Language

    English

    First Page

    1573

    Last Page

    1581

    WOS Identifier

    WOS:000295347500014

    ISSN

    1543-8384

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