Literature DB >> 16645150

Stem cells as a source of regenerative cardiomyocytes.

Keiichi Fukuda1, Shinsuke Yuasa.   

Abstract

The realization of regenerative cardiac medicine depends on the availability of cardiomyocytes in sufficient numbers for transplantation of cardiac tissue and the accompanying blood vessels. Embryonic stem (ES) cells, bone marrow (BM) stem cells, and tissue-derived stem cells are all potential cell sources. Although ES cells are highly proliferative and suitable for mass production, an efficient protocol is yet to be established to ensure selective cardiomyocyte induction using these cells. Recent advances in developmental biology have clarified the involvement of critical factors in cardiomyocyte differentiation, including bone morphogenic protein and Wnt signaling proteins, and such factors have the potential to improve the efficiency of stem cell induction. Initial studies of the intracoronary administration of BM mononuclear cells after myocardial infarction has yielded promising results; however, intensive investigation of the underlying molecular mechanisms at play as well as double-blinded clinical trials will be necessary to establish the extent of both migration of the BM stem cells into the damaged cardiac tissue and their differentiation into cardiomyocytes. Several types of cardiac tissue stem cells have also been reported, but an accurate and extensive comparison of these cells with regard to their characteristics and multipotency remains to be done. An integrative study involving developmental biology, stem cell biology, and tissue engineering is required to achieve the full potential of cardiac regeneration.

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Year:  2006        PMID: 16645150     DOI: 10.1161/01.RES.0000218272.18669.6e

Source DB:  PubMed          Journal:  Circ Res        ISSN: 0009-7330            Impact factor:   17.367


  36 in total

Review 1.  The paracrine effect: pivotal mechanism in cell-based cardiac repair.

Authors:  Simon Maltais; Jacques P Tremblay; Louis P Perrault; Hung Q Ly
Journal:  J Cardiovasc Transl Res       Date:  2010-06-08       Impact factor: 4.132

2.  Cardiac induction of embryonic stem cells by a small molecule inhibitor of Wnt/β-catenin signaling.

Authors:  Hanmin Wang; Jijun Hao; Charles C Hong
Journal:  ACS Chem Biol       Date:  2010-11-24       Impact factor: 5.100

3.  Intravenous administration of atorvastatin-pretreated mesenchymal stem cells improves cardiac performance after acute myocardial infarction: role of CXCR4.

Authors:  Na Li; Yue-Jin Yang; Hai-Yan Qian; Qing Li; Qian Zhang; Xiang-Dong Li; Qiu-Ting Dong; Hui Xu; Lei Song; Hao Zhang
Journal:  Am J Transl Res       Date:  2015-06-15       Impact factor: 4.060

4.  A novel two-step procedure to expand cardiac Sca-1+ cells clonally.

Authors:  Yao Liang Tang; Leping Shen; Keping Qian; M Ian Phillips
Journal:  Biochem Biophys Res Commun       Date:  2007-06-11       Impact factor: 3.575

5.  Progenitor cells isolated from the human heart: a potential cell source for regenerative therapy.

Authors:  P van Vliet; M Roccio; A M Smits; A A M van Oorschot; C H G Metz; T A B van Veen; J P G Sluijter; P A Doevendans; M-J Goumans
Journal:  Neth Heart J       Date:  2008-05       Impact factor: 2.380

6.  Substrate stiffness affects the functional maturation of neonatal rat ventricular myocytes.

Authors:  Jeffrey G Jacot; Andrew D McCulloch; Jeffrey H Omens
Journal:  Biophys J       Date:  2008-06-27       Impact factor: 4.033

7.  The caspase-8 shRNA-modified mesenchymal stem cells improve the function of infarcted heart.

Authors:  Yeyou Liang; Qiuxiong Lin; Jiening Zhu; Xiaohong Li; Yongheng Fu; Xiao Zou; Xiaoying Liu; Honghong Tan; Chunyu Deng; Xiyong Yu; Zhixin Shan; Weiwei Yuan
Journal:  Mol Cell Biochem       Date:  2014-07-25       Impact factor: 3.396

8.  Prevention of acute liver allograft rejection by IL-10-engineered mesenchymal stem cells.

Authors:  J Niu; W Yue; Y Song; Y Zhang; X Qi; Z Wang; B Liu; H Shen; X Hu
Journal:  Clin Exp Immunol       Date:  2014-06       Impact factor: 4.330

9.  Ah Receptor Activation by Dioxin Disrupts Activin, BMP, and WNT Signals During the Early Differentiation of Mouse Embryonic Stem Cells and Inhibits Cardiomyocyte Functions.

Authors:  Qin Wang; Hisaka Kurita; Vinicius Carreira; Chia-I Ko; Yunxia Fan; Xiang Zhang; Jacek Biesiada; Mario Medvedovic; Alvaro Puga
Journal:  Toxicol Sci       Date:  2015-11-15       Impact factor: 4.849

10.  Endogenous Wnt/beta-catenin signaling is required for cardiac differentiation in human embryonic stem cells.

Authors:  Sharon L Paige; Tomoaki Osugi; Olga K Afanasiev; Lil Pabon; Hans Reinecke; Charles E Murry
Journal:  PLoS One       Date:  2010-06-15       Impact factor: 3.240

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