Regeneration of cardiomyocytes from bone marrow: Use of mesenchymal stem cell for cardiovascular tissue engineering

[1]  S. Ogawa,et al.  Bone Marrow–Derived Regenerated Cardiomyocytes (CMG Cells) Express Functional Adrenergic and Muscarinic Receptors , 2002, Circulation.

[2]  P. Libby,et al.  Host bone-marrow cells are a source of donor intimal smooth- muscle–like cells in murine aortic transplant arteriopathy , 2001, Nature Medicine.

[3]  S. Homma,et al.  Neovascularization of ischemic myocardium by human bone-marrow–derived angioblasts prevents cardiomyocyte apoptosis, reduces remodeling and improves cardiac function , 2001, Nature Medicine.

[4]  T. Opthof,et al.  If Current and Spontaneous Activity in Mouse Embryonic Ventricular Myocytes , 2001, Circulation research.

[5]  K. Fukuda,et al.  Development of regenerative cardiomyocytes from mesenchymal stem cells for cardiovascular tissue engineering. , 2001, Artificial organs.

[6]  Hideyuki Okano,et al.  In vitro neurogenesis by progenitor cells isolated from the adult human hippocampus , 2000, Nature Medicine.

[7]  S. Ogawa,et al.  Cardiomyocytes can be generated from marrow stromal cells in vitro. , 1999, The Journal of clinical investigation.

[8]  G Cossu,et al.  Muscle regeneration by bone marrow-derived myogenic progenitors. , 1998, Science.

[9]  D. Prockop.  Marrow Stromal Cells as Stem Cells for Nonhematopoietic Tissues , 1997, Science.

[10]  R. Lefkowitz,et al.  Cardiac function in genetically engineered mice with altered adrenergic receptor signaling. , 1997, The American journal of physiology.

[11]  H. Colecraft,et al.  Does mammalian heart contain only the M2 muscarinic receptor subtype? , 1997, Life sciences.

[12]  C. Long,et al.  Alpha1-adrenergic receptor subtype mRNAs are differentially regulated by alpha1-adrenergic and other hypertrophic stimuli in cardiac myocytes in culture and in vivo. Repression of alpha1B and alpha1D but induction of alpha1C. , 1996, The Journal of biological chemistry.

[13]  D. Zamanillo,et al.  Molecular Cloning of α1d‐Adrenergic Receptor and Tissue Distribution of Three α1‐Adrenergic Receptor Subtypes in Mouse , 1995 .

[14]  S. Okamoto,et al.  Virginiae Butanolide Binding Protein from Streptomyces virginiae , 1995, The Journal of Biological Chemistry.

[15]  K. Kameyama,et al.  Characterization of G Family G Proteins G (G), G (G), and G Expressed in the Baculovirus-Insect Cell System (*) , 1995, The Journal of Biological Chemistry.

[16]  W. Claycomb,et al.  Cardiomyocyte Transfer into the Mammalian Heart , 1995, Annals of the New York Academy of Sciences.

[17]  K. Kameyama,et al.  Characterization of Gq family G proteins GL1 alpha (G14 alpha), GL2 alpha (G11 alpha), and Gq alpha expressed in the baculovirus-insect cell system. , 1995, The Journal of biological chemistry.

[18]  D. Zamanillo,et al.  Molecular cloning of alpha 1d-adrenergic receptor and tissue distribution of three alpha 1-adrenergic receptor subtypes in mouse. , 1995, Journal of neurochemistry.

[19]  Philippe Soriano,et al.  Transcriptional enhancer factor 1 disruption by a retroviral gene trap leads to heart defects and embryonic lethality in mice. , 1994, Genes & development.

[20]  C. Long,et al.  Cloning of the rat alpha 1C-adrenergic receptor from cardiac myocytes. alpha 1C, alpha 1B, and alpha 1D mRNAs are present in cardiac myocytes but not in cardiac fibroblasts. , 1994, Circulation research.

[21]  G. Lyons,et al.  Mef2 gene expression marks the cardiac and skeletal muscle lineages during mouse embryogenesis. , 1994, Development.

[22]  G. Koh,et al.  Formation of nascent intercalated disks between grafted fetal cardiomyocytes and host myocardium. , 1994, Science.

[23]  B. Shenker,et al.  Induction of rapid osteoblast differentiation in rat bone marrow stromal cell cultures by dexamethasone and BMP-2. , 1994, Developmental biology.

[24]  G. Lyons,et al.  Mef 2 gene expression marks the cardiac and skeletal muscle lineages during mouse embryogenesis , 1994 .

[25]  L Hartley,et al.  Nkx-2.5: a novel murine homeobox gene expressed in early heart progenitor cells and their myogenic descendants. , 1993, Development.

[26]  Simon,et al.  Mouse GATA-4: a retinoic acid-inducible GATA-binding transcription factor expressed in endodermally derived tissues and heart , 1993, Molecular and cellular biology.

[27]  E. Ross,et al.  Reconstitution of agonist-stimulated phosphatidylinositol 4,5-bisphosphate hydrolysis using purified m1 muscarinic receptor, Gq/11, and phospholipase C-beta 1. , 1992, The Journal of biological chemistry.

[28]  G. Wallukat,et al.  Pluripotent mouse embryonic stem cells are able to differentiate into cardiomyocytes expressing chronotropic responses to adrenergic and cholinergic agents and Ca2+ channel blockers. , 1991, Differentiation; research in biological diversity.

[29]  A. Friedenstein,et al.  Bone marrow osteogenic stem cells: in vitro cultivation and transplantation in diffusion chambers , 1987, Cell and tissue kinetics.

[30]  C. R. Howlett,et al.  Formation of bone and cartilage by marrow stromal cells in diffusion chambers in vivo. , 1980, Clinical orthopaedics and related research.