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  • 1
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    Nature Publishing Group (NPG)
    Publication Date: 2011-05-20
    Description: Heart failure plagues industrialized nations, killing more people than any other disease. It usually results from a deficiency of specialized cardiac muscle cells known as cardiomyocytes, and a robust therapy to regenerate lost myocardium could help millions of patients every year. Heart regeneration is well documented in amphibia and fish and in developing mammals. After birth, however, human heart regeneration becomes limited to very slow cardiomyocyte replacement. Several experimental strategies to remuscularize the injured heart using adult stem cells and pluripotent stem cells, cellular reprogramming and tissue engineering are in progress. Although many challenges remain, these interventions may eventually lead to better approaches to treat or prevent heart failure.〈br /〉〈br /〉〈a href="https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4091722/" target="_blank"〉〈img src="https://static.pubmed.gov/portal/portal3rc.fcgi/4089621/img/3977009" border="0"〉〈/a〉   〈a href="https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4091722/" target="_blank"〉This paper as free author manuscript - peer-reviewed and accepted for publication〈/a〉〈br /〉〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Laflamme, Michael A -- Murry, Charles E -- P01 HL094374/HL/NHLBI NIH HHS/ -- R01 HL084642/HL/NHLBI NIH HHS/ -- UL1 RR025014/RR/NCRR NIH HHS/ -- England -- Nature. 2011 May 19;473(7347):326-35. doi: 10.1038/nature10147.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Department of Pathology, Center for Cardiovascular Biology, Institute for Stem Cell and Regenerative Medicine, University of Washington, Seattle, Washington 98109, USA.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/21593865" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; Cellular Reprogramming ; Heart/growth & development/physiology ; Heart Failure/genetics/*pathology/surgery/*therapy ; Humans ; Myocytes, Cardiac/cytology/pathology ; Regeneration/genetics/*physiology ; *Regenerative Medicine/methods ; Stem Cell Transplantation
    Print ISSN: 0028-0836
    Electronic ISSN: 1476-4687
    Topics: Biology , Chemistry and Pharmacology , Medicine , Natural Sciences in General , Physics
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  • 2
    Publication Date: 2012-06-05
    Description: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Palpant, Nathan J -- Murry, Charles E -- England -- Nature. 2012 May 31;485(7400):585-6. doi: 10.1038/485585a.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/22660313" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; *Cell Transdifferentiation ; *Cellular Reprogramming ; Female ; Fibroblasts/*cytology ; Heart/*physiology ; Male ; Myocardial Infarction/*therapy ; Myocytes, Cardiac/*cytology/*physiology ; Regenerative Medicine/*methods ; Transcription Factors/*metabolism
    Print ISSN: 0028-0836
    Electronic ISSN: 1476-4687
    Topics: Biology , Chemistry and Pharmacology , Medicine , Natural Sciences in General , Physics
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  • 3
    Publication Date: 2014-04-30
    Description: Pluripotent stem cells provide a potential solution to current epidemic rates of heart failure by providing human cardiomyocytes to support heart regeneration. Studies of human embryonic-stem-cell-derived cardiomyocytes (hESC-CMs) in small-animal models have shown favourable effects of this treatment. However, it remains unknown whether clinical-scale hESC-CM transplantation is feasible, safe or can provide sufficient myocardial regeneration. Here we show that hESC-CMs can be produced at a clinical scale (more than one billion cells per batch) and cryopreserved with good viability. Using a non-human primate model of myocardial ischaemia followed by reperfusion, we show that cryopreservation and intra-myocardial delivery of one billion hESC-CMs generates extensive remuscularization of the infarcted heart. The hESC-CMs showed progressive but incomplete maturation over a 3-month period. Grafts were perfused by host vasculature, and electromechanical junctions between graft and host myocytes were present within 2 weeks of engraftment. Importantly, grafts showed regular calcium transients that were synchronized to the host electrocardiogram, indicating electromechanical coupling. In contrast to small-animal models, non-fatal ventricular arrhythmias were observed in hESC-CM-engrafted primates. Thus, hESC-CMs can remuscularize substantial amounts of the infarcted monkey heart. Comparable remuscularization of a human heart should be possible, but potential arrhythmic complications need to be overcome.〈br /〉〈br /〉〈a href="https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4154594/" target="_blank"〉〈img src="https://static.pubmed.gov/portal/portal3rc.fcgi/4089621/img/3977009" border="0"〉〈/a〉   〈a href="https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4154594/" target="_blank"〉This paper as free author manuscript - peer-reviewed and accepted for publication〈/a〉〈br /〉〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Chong, James J H -- Yang, Xiulan -- Don, Creighton W -- Minami, Elina -- Liu, Yen-Wen -- Weyers, Jill J -- Mahoney, William M -- Van Biber, Benjamin -- Cook, Savannah M -- Palpant, Nathan J -- Gantz, Jay A -- Fugate, James A -- Muskheli, Veronica -- Gough, G Michael -- Vogel, Keith W -- Astley, Cliff A -- Hotchkiss, Charlotte E -- Baldessari, Audrey -- Pabon, Lil -- Reinecke, Hans -- Gill, Edward A -- Nelson, Veronica -- Kiem, Hans-Peter -- Laflamme, Michael A -- Murry, Charles E -- P01 GM081619/GM/NIGMS NIH HHS/ -- P01 HL094374/HL/NHLBI NIH HHS/ -- P01GM081619/GM/NIGMS NIH HHS/ -- P01HL094374/HL/NHLBI NIH HHS/ -- P51 OD010425/OD/NIH HHS/ -- R01 HL084642/HL/NHLBI NIH HHS/ -- R01 HL117991/HL/NHLBI NIH HHS/ -- R01HL084642/HL/NHLBI NIH HHS/ -- T32 GM007266/GM/NIGMS NIH HHS/ -- U01 HL100405/HL/NHLBI NIH HHS/ -- U01HL100405/HL/NHLBI NIH HHS/ -- England -- Nature. 2014 Jun 12;510(7504):273-7. doi: 10.1038/nature13233. Epub 2014 Apr 30.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉1] Center for Cardiovascular Biology, University of Washington, Seattle, Washington 98109, USA [2] Institute for Stem Cell and Regenerative Medicine, University of Washington, Seattle, Washington 98109, USA [3] Department of Cardiology Westmead Hospital, Westmead, New South Wales 2145, Australia [4] School of Medicine, University of Sydney, Sydney, New South Wales 2006, Australia [5] Department of Pathology, University of Washington, Seattle, Washington 98195, USA [6] University of Sydney School of Medicine, Sydney, New South Wales 2006, Australia and Westmead Millennium Institute and Westmead Hospital, Westmead, New South Wales 2145, Australia. ; 1] Center for Cardiovascular Biology, University of Washington, Seattle, Washington 98109, USA [2] Institute for Stem Cell and Regenerative Medicine, University of Washington, Seattle, Washington 98109, USA [3] Department of Pathology, University of Washington, Seattle, Washington 98195, USA. ; Department of Medicine/Cardiology, University of Washington, Seattle, Washington 98195, USA. ; 1] Center for Cardiovascular Biology, University of Washington, Seattle, Washington 98109, USA [2] Institute for Stem Cell and Regenerative Medicine, University of Washington, Seattle, Washington 98109, USA [3] Department of Pathology, University of Washington, Seattle, Washington 98195, USA [4] Department of Medicine/Cardiology, University of Washington, Seattle, Washington 98195, USA. ; Department of Comparative Medicine, Institute for Stem Cell and Regenerative Medicine, University of Washington, Seattle, Washington 98109, USA. ; 1] Center for Cardiovascular Biology, University of Washington, Seattle, Washington 98109, USA [2] Institute for Stem Cell and Regenerative Medicine, University of Washington, Seattle, Washington 98109, USA [3] Department of Pathology, University of Washington, Seattle, Washington 98195, USA [4] Department of Bioengineering, University of Washington, Seattle, Washington 98195, USA. ; Washington National Primate Research Center, University of Washington, Seattle, Washington 98195, USA. ; Fred Hutchinson Cancer Research Center, Seattle, Washington 98109, USA. ; 1] Department of Pathology, University of Washington, Seattle, Washington 98195, USA [2] Fred Hutchinson Cancer Research Center, Seattle, Washington 98109, USA. ; 1] Center for Cardiovascular Biology, University of Washington, Seattle, Washington 98109, USA [2] Institute for Stem Cell and Regenerative Medicine, University of Washington, Seattle, Washington 98109, USA [3] Department of Pathology, University of Washington, Seattle, Washington 98195, USA [4] Department of Medicine/Cardiology, University of Washington, Seattle, Washington 98195, USA [5] Department of Bioengineering, University of Washington, Seattle, Washington 98195, USA.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/24776797" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; Arrhythmias, Cardiac/physiopathology ; Calcium/metabolism ; Cell Survival ; Coronary Vessels/physiology ; Cryopreservation ; Disease Models, Animal ; Electrocardiography ; Embryonic Stem Cells/*cytology ; *Heart ; Humans ; Macaca nemestrina ; Male ; Mice ; Myocardial Infarction/*pathology/*therapy ; Myocytes, Cardiac/*cytology ; *Regeneration ; Regenerative Medicine/methods
    Print ISSN: 0028-0836
    Electronic ISSN: 1476-4687
    Topics: Biology , Chemistry and Pharmacology , Medicine , Natural Sciences in General , Physics
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  • 4
    Publication Date: 2012-08-07
    Description: Transplantation studies in mice and rats have shown that human embryonic-stem-cell-derived cardiomyocytes (hESC-CMs) can improve the function of infarcted hearts, but two critical issues related to their electrophysiological behaviour in vivo remain unresolved. First, the risk of arrhythmias following hESC-CM transplantation in injured hearts has not been determined. Second, the electromechanical integration of hESC-CMs in injured hearts has not been demonstrated, so it is unclear whether these cells improve contractile function directly through addition of new force-generating units. Here we use a guinea-pig model to show that hESC-CM grafts in injured hearts protect against arrhythmias and can contract synchronously with host muscle. Injured hearts with hESC-CM grafts show improved mechanical function and a significantly reduced incidence of both spontaneous and induced ventricular tachycardia. To assess the activity of hESC-CM grafts in vivo, we transplanted hESC-CMs expressing the genetically encoded calcium sensor, GCaMP3 (refs 4, 5). By correlating the GCaMP3 fluorescent signal with the host ECG, we found that grafts in uninjured hearts have consistent 1:1 host-graft coupling. Grafts in injured hearts are more heterogeneous and typically include both coupled and uncoupled regions. Thus, human myocardial grafts meet physiological criteria for true heart regeneration, providing support for the continued development of hESC-based cardiac therapies for both mechanical and electrical repair.〈br /〉〈br /〉〈a href="https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3443324/" target="_blank"〉〈img src="https://static.pubmed.gov/portal/portal3rc.fcgi/4089621/img/3977009" border="0"〉〈/a〉   〈a href="https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3443324/" target="_blank"〉This paper as free author manuscript - peer-reviewed and accepted for publication〈/a〉〈br /〉〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Shiba, Yuji -- Fernandes, Sarah -- Zhu, Wei-Zhong -- Filice, Dominic -- Muskheli, Veronica -- Kim, Jonathan -- Palpant, Nathan J -- Gantz, Jay -- Moyes, Kara White -- Reinecke, Hans -- Van Biber, Benjamin -- Dardas, Todd -- Mignone, John L -- Izawa, Atsushi -- Hanna, Ramy -- Viswanathan, Mohan -- Gold, Joseph D -- Kotlikoff, Michael I -- Sarvazyan, Narine -- Kay, Matthew W -- Murry, Charles E -- Laflamme, Michael A -- K08 HL080431/HL/NHLBI NIH HHS/ -- K08-HL80431/HL/NHLBI NIH HHS/ -- P01 GM081619/GM/NIGMS NIH HHS/ -- P01 HL094374/HL/NHLBI NIH HHS/ -- P01-GM81619/GM/NIGMS NIH HHS/ -- P01-HL094374/HL/NHLBI NIH HHS/ -- R01 HL064387/HL/NHLBI NIH HHS/ -- R01 HL084642/HL/NHLBI NIH HHS/ -- R01 HL095828/HL/NHLBI NIH HHS/ -- R01-HL064387/HL/NHLBI NIH HHS/ -- R01-HL084642/HL/NHLBI NIH HHS/ -- R01-HL095828/HL/NHLBI NIH HHS/ -- U01 HL100405/HL/NHLBI NIH HHS/ -- U01-HL100405/HL/NHLBI NIH HHS/ -- U24 DK076126/DK/NIDDK NIH HHS/ -- U24-DK076126/DK/NIDDK NIH HHS/ -- England -- Nature. 2012 Sep 13;489(7415):322-5. doi: 10.1038/nature11317.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Department of Pathology, Center for Cardiovascular Biology, Institute for Stem Cell and Regenerative Medicine, University of Washington, Seattle, Washington 98109, USA.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/22864415" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; Arrhythmias, Cardiac/etiology/physiopathology/*therapy ; Calcium/analysis/metabolism ; Electric Stimulation ; *Electrophysiological Phenomena ; Embryonic Stem Cells/*cytology ; Fluorescent Dyes/analysis ; Guinea Pigs ; Heart Injuries/complications/pathology/*physiopathology ; Humans ; Luminescent Measurements ; Male ; Myocardial Contraction/physiology ; Myocardium/cytology/*pathology ; Myocytes, Cardiac/*cytology/physiology/*transplantation ; Tachycardia, Ventricular/etiology/physiopathology/therapy
    Print ISSN: 0028-0836
    Electronic ISSN: 1476-4687
    Topics: Biology , Chemistry and Pharmacology , Medicine , Natural Sciences in General , Physics
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  • 5
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 2009-04-04
    Description: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Murry, Charles E -- Lee, Richard T -- New York, N.Y. -- Science. 2009 Apr 3;324(5923):47-8. doi: 10.1126/science.1172255.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Department of Pathology, Center for Cardiovascular Biology, Institute for Stem Cell and Regenerative Medicine, University of Washington, Seattle, WA 98109, USA. murry@u.washington.edu〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/19342577" target="_blank"〉PubMed〈/a〉
    Keywords: Adult ; Aged ; Aging ; Carbon Radioisotopes/analysis ; Cell Nucleus Division ; Cell Proliferation ; DNA/analysis/*biosynthesis ; Humans ; Middle Aged ; Myocytes, Cardiac/*cytology/metabolism ; Nuclear Weapons ; Polyploidy ; Radiometric Dating ; Stem Cells/cytology
    Print ISSN: 0036-8075
    Electronic ISSN: 1095-9203
    Topics: Biology , Chemistry and Pharmacology , Computer Science , Medicine , Natural Sciences in General , Physics
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  • 6
    Publication Date: 2016-05-14
    Description: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Caulfield, Timothy -- Sipp, Douglas -- Murry, Charles E -- Daley, George Q -- Kimmelman, Jonathan -- New York, N.Y. -- Science. 2016 May 13;352(6287):776-7. doi: 10.1126/science.aaf4620. Epub 2016 May 12.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Health Law Institute, University of Alberta, Edmonton, Alberta T6G 2H5, Canada. caulfield@ualberta.ca. ; Riken Center for Developmental Biology, Kobe, Japan, 650-0047. Keio University School of Medicine, Tokyo, Japan, 160-8582. ; Institute for Stem Cell and Regenerative Medicine, University of Washington, Seattle, WA 98109, USA. ; Boston Children's Hospital, Harvard Medical School, Boston, MA 02115, USA. ; STREAM research group, Biomedical Ethics Unit, McGill University, Montreal, Quebec H3A 1X1, Canada.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/27174977" target="_blank"〉PubMed〈/a〉
    Print ISSN: 0036-8075
    Electronic ISSN: 1095-9203
    Topics: Biology , Chemistry and Pharmacology , Computer Science , Medicine , Natural Sciences in General , Physics
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  • 7
    Publication Date: 2016-05-20
    Description: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Kimmelman, Jonathan -- Hyun, Insoo -- Benvenisty, Nissim -- Caulfield, Timothy -- Heslop, Helen E -- Murry, Charles E -- Sipp, Douglas -- Studer, Lorenz -- Sugarman, Jeremy -- Daley, George Q -- England -- Nature. 2016 May 12;533(7603):311-3. doi: 10.1038/533311a.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉McGill University, Montreal, Canada, and a member of the steering committee of the International Society for Stem Cell Research's Guidelines Task Force. ; Case Western Reserve University School of Medicine, USA, and a member of the steering committee of the International Society for Stem Cell Research's Guidelines Task Force. ; Azrieli Center for Stem Cells and Genetic Research, Hebrew University, Jerusalem, Israel, and a member of the steering committee of the International Society for Stem Cell Research's Guidelines Task Force. ; Canada Research Chair in Health Law and Policy at the University of Alberta, Canada, and a member of the steering committee of the International Society for Stem Cell Research's Guidelines Task Force. ; Center for Cell and Gene Therapy at Baylor College of Medicine in Houston, Texas, USA, and a member of the steering committee of the International Society for Stem Cell Research's Guidelines Task Force. ; Departments of Pathology, Bioengineering and Medicine/Cardiology, University of Washington, Seattle, Washington, USA, and a member of the steering committee of the International Society for Stem Cell Research's Guidelines Task Force. ; RIKEN Center for Developmental Biology, Kobe, Japan, project professor at Keio University School of Medicine, Tokyo, Japan, and a member of the steering committee of the International Society for Stem Cell Research's Guidelines Task Force. ; Developmental Biology Program and director of the Center for Stem Cell Biology, Memorial Sloan Kettering Cancer Center, USA, and a member of the steering committee of the International Society for Stem Cell Research's Guidelines Task Force. ; Berman Institute of Bioethics and Department of Medicine, Johns Hopkins University, Baltimore, Maryland, USA, and a member of the steering committee of the International Society for Stem Cell Research's Guidelines Task Force. ; Boston Children's Hospital and Harvard Medical School, Boston, Massachusetts, USA, and a member of the steering committee of the International Society for Stem Cell Research's Guidelines Task Force.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/27193661" target="_blank"〉PubMed〈/a〉
    Print ISSN: 0028-0836
    Electronic ISSN: 1476-4687
    Topics: Biology , Chemistry and Pharmacology , Medicine , Natural Sciences in General , Physics
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  • 8
  • 9
    Publication Date: 2013-04-10
    Description: We previously demonstrated that cardiac myosin can use 2-deoxy-ATP (dATP) as an energy substrate, that it enhances contraction and relaxation with minimal effect on calcium-handling properties in vitro, and that contractile enhancement occurs with only minor elevation of cellular [dATP]. Here, we report the effect of chronically enhanced dATP concentration...
    Print ISSN: 0027-8424
    Electronic ISSN: 1091-6490
    Topics: Biology , Medicine , Natural Sciences in General
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  • 10
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