Epigenetics, cardiovascular disease, and cellular reprogramming

被引:25
作者
Al-Hasani, Keith [1 ]
Mathiyalagan, Prabhu [2 ]
El-Osta, Assam [1 ,3 ]
机构
[1] Monash Univ, Dept Diabet, Epigenet Human Hlth & Dis Lab, Melbourne, Vic, Australia
[2] Icahn Sch Med Mt Sinai, Cardiovasc Res Ctr, New York, NY 10029 USA
[3] Chinese Univ Hong Kong, Prince Wales Hosp, Hong Kong Inst Diabet & Obes, Hong Kong, Peoples R China
基金
中国国家自然科学基金; 英国医学研究理事会;
关键词
GENE-EXPRESSION; CARDIAC-HYPERTROPHY; HISTONE DEACETYLATION; STEM-CELLS; INHIBITION; MICRORNA; DIFFERENTIATION; PROMOTES; METHYLATION; FIBROBLASTS;
D O I
10.1016/j.yjmcc.2019.01.019
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Under the seeming disorder of "junk" sequences the last decade has seen developments in our understanding of non-coding RNA's (ncRNAs). Its a complex revised order and nowhere is this more relevant than in the developing heart whereby old rules have been set aside to make room for new ones. The development of the mammalian heart has been studied at the genetic and cellular level for several decades because these areas were considered ideal control points. As such, detailed mechanisms governing cell lineages are well described. Emerging evidence suggests a complex new order regulated by epigenetic mechanisms mark cardiac cell lineage. Indeed, molecular cardiologists are in the process of shedding light on the roles played by ncRNAs, nucleic acid methylation and histone/chromatin modifications in specific pathologies of the heart. The aim of this article is to discuss some of the recent advances in the field of cardiovascular epigenetics that are related to direct cell reprogramming and repair. As such, we explore ncRNAs as nodes regulating signaling networks and attempt to make sense of regulatory disorder by reinforcing the importance of epigenetic components in the developmental program.
引用
收藏
页码:129 / 133
页数:5
相关论文
共 77 条
[1]   Adult Duct-Lining Cells Can Reprogram into β-like Cells Able to Counter Repeated Cycles of Toxin-Induced Diabetes [J].
Al-Hasani, Keith ;
Pfeifer, Anja ;
Courtney, Monica ;
Ben-Othman, Nouha ;
Gjernes, Elisabet ;
Vieira, Andhira ;
Druelle, Noemie ;
Avolio, Fabio ;
Ravassard, Philippe ;
Leuckx, Gunter ;
Lacas-Gervais, Sandra ;
Ambrosetti, Damien ;
Benizri, Emmanuel ;
Hecksher-Sorensen, Jacob ;
Gounon, Pierre ;
Ferrer, Jorge ;
Gradwohl, Gerard ;
Heimberg, Harry ;
Mansouri, Ahmed ;
Collombat, Patrick .
DEVELOPMENTAL CELL, 2013, 26 (01) :86-100
[2]   NKX2-5 regulates human cardiomyogenesis via a HEY2 dependent transcriptional network [J].
Anderson, David J. ;
Kaplan, David I. ;
Bell, Katrina M. ;
Koutsis, Katerina ;
Haynes, John M. ;
Mills, Richard J. ;
Phelan, Dean G. ;
Qian, Elizabeth L. ;
Leitoguinho, Ana Rita ;
Arasaratnam, Deevina ;
Labonne, Tanya ;
Ng, Elizabeth S. ;
Davis, Richard P. ;
Casini, Simona ;
Passier, Robert ;
Hudson, James E. ;
Porrello, Enzo R. ;
Costa, Mauro W. ;
Rafii, Arash ;
Curl, Clare L. ;
Delbridge, Lea M. ;
Harvey, Richard P. ;
Oshlack, Alicia ;
Cheung, Michael M. ;
Mummery, Christine L. ;
Petrou, Stephen ;
Elefanty, Andrew G. ;
Stanley, Edouard G. ;
Elliott, David A. .
NATURE COMMUNICATIONS, 2018, 9
[3]   Long-Term GABA Administration Induces Alpha Cell-Mediated Beta-like Cell Neogenesis [J].
Ben-Othman, Nouha ;
Vieira, Andhira ;
Courtney, Monica ;
Record, Fabien ;
Gjernes, Elisabet ;
Avolio, Fabio ;
Hadzic, Biljana ;
Druelle, Noemie ;
Napolitano, Tiziana ;
Navarro-Sanz, Sergi ;
Silvano, Serena ;
Al-Hasani, Keith ;
Pfeifer, Anja ;
Lacas-Gervais, Sandra ;
Leuckx, Gunter ;
Marroqui, Laura ;
Thevenet, Julien ;
Madsen, Ole Dragsbaek ;
Eizirik, Decio Laks ;
Heimberg, Harry ;
Kerr-Conte, Julie ;
Pattou, Francois ;
Mansouri, Ahmed ;
Collombat, Patrick .
CELL, 2017, 168 (1-2) :73-+
[4]   Hallmarks of ion channel gene expression in end-stage heart failure [J].
Borlak, J ;
Thum, T .
FASEB JOURNAL, 2003, 17 (12) :1592-1608
[5]   Genetic and Epigenetic Regulation of Human Cardiac Reprogramming and Differentiation in Regenerative Medicine [J].
Burridge, Paul W. ;
Sharma, Arun ;
Wu, Joseph C. .
ANNUAL REVIEW OF GENETICS, VOL 49, 2015, 49 :461-484
[6]   Histone deacetylase (HDAC) inhibitors attenuate cardiac hypertrophy by suppressing autophagy [J].
Cao, Dian J. ;
Wang, Zhao V. ;
Battiprolu, Pavan K. ;
Jiang, Nan ;
Morales, Cyndi R. ;
Kong, Yongli ;
Rothermel, Beverly A. ;
Gillette, Thomas G. ;
Hill, Joseph A. .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2011, 108 (10) :4123-4128
[7]   Histone deacetylases facilitate sodium/calcium exchanger up-regulation in adult cardiomyocytes [J].
Chandrasekaran, Sangeetha ;
Peterson, Richard E. ;
Mani, Santhosh K. ;
Addy, Benjamin ;
Buchholz, Avery L. ;
Xu, Lin ;
Thiyagarajan, Thirumagal ;
Kasiganesan, Harinath ;
Kern, Christine B. ;
Menick, Donald R. .
FASEB JOURNAL, 2009, 23 (11) :3851-3864
[8]   Cardiac genes show contextual SWI/SNF interactions with distinguishable gene activities [J].
Chang, Lisa ;
Kiriazis, Helen ;
Gao, Xiao-Ming ;
Du, Xiao-Jun ;
El-Osta, Assam .
EPIGENETICS, 2011, 6 (06) :760-768
[9]   Targeted deletion of Dicer in the heart leads to dilated cardiomyopathy and heart failure [J].
Chen, Jian-Fu ;
Murchison, Elizabeth P. ;
Tang, Ruhang ;
Callis, Thomas E. ;
Tatsuguchi, Mariko ;
Deng, Zhongliang ;
Rojas, Mauricio ;
Hammond, Scott M. ;
Schneider, Michael D. ;
Selzman, Craig H. ;
Meissner, Gerhard ;
Patterson, Cam ;
Hannon, Gregory J. ;
Wang, Da-Zhi .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2008, 105 (06) :2111-2116
[10]   Direct Gingival Fibroblast/Osteoblast Transdifferentiation via Epigenetics [J].
Cho, Y. ;
Kim, B. ;
Bae, H. ;
Kim, W. ;
Baek, J. ;
Woo, K. ;
Lee, G. ;
Seol, Y. ;
Lee, Y. ;
Ku, Y. ;
Rhyu, I. ;
Ryoo, H. .
JOURNAL OF DENTAL RESEARCH, 2017, 96 (05) :555-561