Neonatal heart-enriched miR-708 promotes differentiation of cardiac progenitor cells in rats

International Journal of Molecular Sciences

Volumn 17, Issue 6, 2016, Pages

  Deng, Shengqiong ^a,b   Zhao, Qian ^a   Zhou, Xianjin ^a   Zhang, Lin ^a   Bao, Luer ^a   Zhen, Lixiao ^a   Zhang, Yuzhen ^a   Fan, Huimin ^a   Liu, Zhongmin ^a   Yu, Zuoren ^a  

^a TONGJI UNIVERSITY SCHOOL OF MEDICINE   (China)

^b SECOND MILITARY MEDICAL UNIVERSITY   (China)

Author keywords

Cardiac stem progenitor cells; Cardiomyocytes; Heart regeneration; MiR 708

Indexed keywords

MICRORNA; MICRORNA 708; PEROXISOME PROLIFERATOR ACTIVATED RECEPTOR ALPHA; STEM CELL FACTOR RECEPTOR; TRANSCRIPTION FACTOR NKX2.5; UNCLASSIFIED DRUG; TRANSCRIPTOME;

ANIMAL CELL; ARTICLE; CARDIAC MUSCLE CELL; CARDIAC STEM CELL; CARDIAC TROPONIN 1 CLIA; CARDIAC TROPONIN T TYPE 2; CARDIOVASCULAR DISEASE; CELL DIFFERENTIATION; CELL REGENERATION; CONTROLLED STUDY; FIBROBLAST; FLUORESCENCE ACTIVATED CELL SORTER; IMMUNOFLUORESCENCE; NEWBORN; NONHUMAN; PROTEIN EXPRESSION; RAT; REAL TIME POLYMERASE CHAIN REACTION; ANIMAL; CARDIAC MUSCLE; CARDIAC MYOBLAST; CLUSTER ANALYSIS; CYTOLOGY; GENE EXPRESSION PROFILING; GENETICS; METABOLISM; REGENERATION;

ANIMALS; ANIMALS, NEWBORN; CELL DIFFERENTIATION; CLUSTER ANALYSIS; GENE EXPRESSION PROFILING; MICRORNAS; MYOBLASTS, CARDIAC; MYOCARDIUM; MYOCYTES, CARDIAC; RATS; REGENERATION; TRANSCRIPTOME;

EID: 84973322291     PISSN: 16616596     EISSN: 14220067     Source Type: Journal    
DOI: 10.3390/ijms17060875     Document Type: Article

References (24)

1. Beltrami, A.P.; Barlucchi, L.; Torella, D.; Baker, M.; Limana, F.; Chimenti, S.; Kasahara, H.; Rota, M.; Musso, E.; Urbanek, K. Adult cardiac stem cells are multipotent and support myocardial regeneration. Cell 2003, 114, 763-776. [CrossRef]
2. Li, F.; Wang, X.; Capasso, J.M.; Gerdes, A.M. Rapid transition of cardiac myocytes from hyperplasia to hypertrophy during postnatal development. J. Mol. Cell. Cardiol. 1996, 28, 1737-1746. [CrossRef] [PubMed]
3. Bu, L.; Jiang, X.; Martin-Puig, S.; Caron, L.; Zhu, S.; Shao, Y.; Roberts, D.J.; Huang, P.L.; Domian, I.J.; Chien, K.R. Human ISL1 heart progenitors generate diverse multipotent cardiovascular cell lineages. Nature 2009, 460, 113-117. [CrossRef] [PubMed]
4. Mouquet, F.; Pfister, O.; Jain, M.; Oikonomopoulos, A.; Ngoy, S.; Summer, R.; Fine, A.; Liao, R. Restoration of cardiac progenitor cells after myocardial infarction by self-proliferation and selective homing of bone marrow-derived stem cells. Circ. Res. 2005, 97, 1090-1092. [CrossRef] [PubMed]
5. Lu, G.; Haider, H.K.; Jiang, S.; Ashraf, M. Sca-1+ stem cell survival and engraftment in the infarcted heart: Dual role for preconditioning-induced connexin-43. Circulation 2009, 119, 2587-2596. [CrossRef] [PubMed]
6. Linke, A.; Müller, P.; Nurzynska, D.; Casarsa, C.; Torella, D.; Nascimbene, A.; Castaldo, C.; Cascapera, S.; Böhm, M.; Quaini, F. Stem cells in the dog heart are self-renewing, clonogenic, and multipotent and regenerate infarcted myocardium, improving cardiac function. Proc. Natl. Acad. Sci. USA 2005, 102, 8966-8971. [CrossRef] [PubMed]
7. Dawn, B.; Stein, A.B.; Urbanek, K.; Rota, M.; Whang, B.; Rastaldo, R.; Torella, D.; Tang, X.L.; Rezazadeh, A.; Kajstura, J. Cardiac stem cells delivered intravascularly traverse the vessel barrier, regenerate infarcted myocardium, and improve cardiac function. Proc. Natl. Acad. Sci. USA 2005, 102, 3766-3771. [CrossRef] [PubMed]
8. Chamuleau, S.A.; Vrijsen, K.R.; Rokosh, D.G.; Tang, X.L.; Piek, J.J.; Bolli, R. Cell therapy for ischaemic heart disease: Focus on the role of resident cardiac stem cells. Neth. Heart J. 2009, 17, 199-207. [CrossRef] [PubMed]
9. Urbanek, K.; Torella, D.; Sheikh, F.; de Angelis, A.; Nurzynska, D.; Silvestri, F.; Beltrami, C.A.; Bussani, R.; Beltrami, A.P.; Quaini, F. Myocardial regeneration by activation of multipotent cardiac stem cells in ischemic heart failure. Proc. Natl. Acad. Sci. USA 2005, 102, 8692-8697. [CrossRef] [PubMed]
10. Stamm, C.; Nasseri, B.; Hetzer, R. Cardiac stem cells in patients with ischaemic cardiomyopathy. Lancet 2012, 379, 891. [CrossRef]
11. Makkar, R.R.; Smith, R.R.; Cheng, K.; Malliaras, K.; Thomson, L.E.; Berman, D.; Czer, L.S.; Marbán, L.; Mendizabal, A.; Johnston, P.V. Intracoronary cardiosphere-derived cells for heart regeneration after myocardial infarction (CADUCEUS): A prospective, randomised phase 1 trial. Lancet 2012, 379, 895-904. [CrossRef]
12. Siu, C.W.; Tse, H.F. Cardiac regeneration: Messages from CADUCEUS. Lancet 2012, 379, 870-871. [CrossRef]
13. Bartel, D.P. MicroRNAs: Genomics, biogenesis, mechanism, and function. Cell 2004, 116, 281-297. [CrossRef]
14. Li, Y.; Liang, C.L.; Ma, H.Z.; Zhao, Q.; Lu, Y.; Xiang, Z.D.; Li, L.; Qin, J.; Chen, Y.J.; Cho, W.C. miR-221/222 promotes S-phase entry and cellular migration in control of basal-like breast cancer. Molecules 2014, 19, 7122-7137. [CrossRef] [PubMed]
15. Cui, Q.; Yu, Z.; Purisima, E.O.; Wang, E. Principles of microRNA regulation of a human cellular signaling network. Mol. Syst. Biol. 2006, 2, 46. [CrossRef] [PubMed]
16. Tili, E.; Michaille, J.J.; Gandhi, V.; Plunkett, W.; Sampath, D.; Calin, G.A. MiRNAs and their potential for use against cancer and other diseases. Future Oncol. 2007, 3, 521-537. [CrossRef] [PubMed]
17. Calin, G.A.; Croce, C.M. MicroRNA signatures in human cancers. Nat. Rev. Cancer 2006, 6, 857-866. [CrossRef] [PubMed]
18. Small, E.M.; Olson, E.N. Pervasive roles of microRNAs in cardiovascular biology. Nature 2011, 469, 336-342. [CrossRef] [PubMed]
19. Smits, A.M.; van Vliet, P.; Metz, C.H.; Korfage, T.; Sluijter, J.P.; Doevendans, P.A.; Goumans, M.J. Hu mancardiomyocyte progenitor cells differentiate into functional mature cardiomyocytes: An in vitro model for studying human cardiac physiology and pathophysiology. Nat. Protoc. 2009, 4, 232-243. [CrossRef] [PubMed]
20. Furtado, K.S.; de Oliveira Andrade, F.; Campos, A.; Rosim, M.P.; Vargas-Mendez, E.; Henriques, A.; de Conti, A.; Scolastici, C.; Barbisan, L.F.; Carvalho, R.F. β-ionone modulates the expression of miRNAs and genes involved in the metastatic phenotype of microdissected persistent preneoplastic lesions in rats submitted to hepatocarcinogenesis. Mol. Carcinog. 2016. [CrossRef] [PubMed]
21. Forstner, A.J.; Forstner, A.J.; Hofmann, A.; Maaser, A.; Sumer, S.; Khudayberdiev, S.; Mühleisen, T.W.; Leber, M.; Schulze, T.G.; Strohmaier, J. Genome-wide analysis implicates microRNAs and their target genes in the development of bipolar disorder. Transl. Psychiatry 2015, 5, e678. [CrossRef] [PubMed]
22. Van Berlo, J.H.; van Berlo, J.H.; Kanisicak, O.; Maillet, M.; Vagnozzi, R.J.; Karch, J.; Lin, S.C.; Middleton, R.C.; Marbán, E.; Molkentin, J.D. c-kit+ cells minimally contribute cardiomyocytes to the heart. Nature 2014, 509, 337-341. [CrossRef] [PubMed]
23. Sultana, N.; Sultana, N.; Zhang, L.; Yan, J.; Chen, J.; Cai, W.; Razzaque, S.; Jeong, D.; Sheng, W.; Bu, L. Resident c-kit(+) cells in the heart are not cardiac stem cells. Nat. Commun. 2015, 6, 8701. [CrossRef] [PubMed]
24. Zhao, Q.; Deng, S.Q.; Wang, G.X.; Liu, C.C.; Meng, L.Y.; Qiao, S.S.; Shen, L.; Zhang, Y.; Lü, J.H.; Li, W.S. A direct quantification method for measuring plasma MicroRNAs identified potential biomarkers for detecting metastatic breast cancer. Oncotarget 2016. [CrossRef]