Investigation of expression pattern of hsa-miR-11181-5p during the course of cardiac progenitor cells differentiation

Document Type : Original Research

Authors

Genetics Department, Faculty of Biological Sciences, Tarbiat Modares University, Tehran, Iran

Abstract
Cardiovascular diseases (CVDs) are globally the number 1 cause of death. Despite improvement in treatment strategies, heart disorders are strongly increasing. Therefore, identification of new regulatory factors involved in the cardiac differentiation is very important. TRKC receptor, part of the large family of receptor tyrosine kinases, is involved in development of the heart and central nervous system. There are many contradictory functions related to the TRKC gene which might be attributed to the non-coding RNAs located in it. Recently, a novel miRNA, hsa-miR-11181-5p located in TRKC gene, has been reported which is involved in nervous differentiation. MiRNAs are small non-coding RNAs regulating their target genes via mRNA degradation or protein inhibition. The goal of the present study was to investigate the expression pattern of hsa-miR-11181-5p during the course of cardiosphere-derived cells (CDCs) differentiation.

Keywords

Subjects


1. Ekhteraei Tousi S, Mohammad Soltani B, Sadeghizadeh M, Hoseini S, Soleimani M. Hsa-miR-133b Expression Profile during Cardiac Progenitor Cell Differentiation and its Inhibitory Effect on SRF Expression. Modares Journal of Medical Sciences: Pathobiology. 2013;16(1):1-9.
2. van Rooij E, Sutherland LB, Liu N, Williams AH, McAnally J, Gerard RD, et al. A signature pattern of stress-responsive microRNAs that can evoke cardiac hypertrophy and heart failure. Proceedings of the National Academy of Sciences. 2006;103(48):18255-60.
3. Ichaso N, Rodriguez RE, Martin-Zanca D, Gonzalez-Sarmiento R. Genomic characterization of the human trkC gene. Oncogene. 1998;17(14):1871-5.
4. Dokanehiifard S, Soltani BM, Parsi S, Hosseini F, Javan M, Mowla SJ. Experimental verification of a conserved intronic microRNA located in the human TrkC gene with a cell type-dependent apoptotic function. Cellular and Molecular Life Sciences. 2015:1-13.
5. Caporali A, Emanueli C. Cardiovascular actions of neurotrophins. Physiological Reviews. 2009;89(1):279-308.
6. Lin MI, Das I, Schwartz GM, Tsoulfas P, Mikawa T, Hempstead BL. Trk C receptor signaling regulates cardiac myocyte proliferation during early heart development in vivo. Developmental biology. 2000;226(2):180-91.
7. Kawaguchi-Manabe H, Ieda M, Kimura K, Manabe T, Miyatake S, Kanazawa H, et al. A novel cardiac hypertrophic factor, neurotrophin-3, is paradoxically downregulated in cardiac hypertrophy. Life sciences. 2007;81(5):385-92.
8. Ekhteraei‐Tousi S, Mohammad‐Soltani B, Sadeghizadeh M, Mowla SJ, Parsi S, Soleimani M. Inhibitory Effect of Hsa‐miR‐590‐5p on Cardiosphere‐derived Stem Cells Differentiation Through Downregulation of TGFB Signaling. Journal of cellular biochemistry. 2015;116(1):179-91.
9. Jafarzadeh M, Soltani BM. Hsa-miR-590-5p Interaction with SMAD3 Transcript Supports Its Regulatory Effect on The TGFβ Signaling Pathway. Cell Journal (Yakhteh). 2016;18(1):7.
10. Smits AM, van Vliet P, Metz CH, Korfage T, Sluijter JP, Doevendans PA, et al. Human cardiomyocyte progenitor cells differentiate into functional mature cardiomyocytes: an in vitro model for studying human cardiac physiology and pathophysiology. Nature protocols. 2009;4(2):232-43.
11. Dokanehiifard S, Yasari A, Najafi H, Jafarzadeh M, Nikkhah M, Mowla SJ, et al. A novel microRNA located in the TrkC gene regulates the Wnt signaling pathway and is differentially expressed in colorectal cancer specimens. Journal of Biological Chemistry. 2017;292(18):7566-77.
12. Saleh AJ, Soltani BM, Dokanehiifard S, Medlej A, Tavalaei M, Mowla SJ. Experimental verification of a predicted novel microRNA located in human PIK3CA gene with a potential oncogenic function in colorectal cancer. Tumor Biology. 2016;37(10):14089-101.
13. Latronico MV, Catalucci D, Condorelli G. Emerging role of microRNAs in cardiovascular biology. Circulation research. 2007;101(12):1225-36.
14. Tanaka M, Chen Z, Bartunkova S, Yamasaki N, Izumo S. The cardiac homeobox gene Csx/Nkx2. 5 lies genetically upstream of multiple genes essential for heart development. Development. 1999;126(6):1269-80.
15. Koh YH, Suzuki K, Che W, Park YS, Miyamoto Y, Higashiyama S, et al. Inactivation of glutathione peroxidase by NO leads to the accumulation of H2O2 and the induction of HB-EGF via c-Jun NH2-terminal kinase in rat aortic smooth muscle cells. The FASEB Journal. 2001;15(8):1472-4.
16. Ushikoshi H, Takahashi T, Chen X, Khai NC, Esaki M, Goto K, et al. Local overexpression of HB-EGF exacerbates remodeling following myocardial infarction by activating noncardiomyocytes. Laboratory investigation. 2005;85(7):862-73.
17. Cao F, Wagner RA, Wilson KD, Xie X, Fu J-D, Drukker M, et al. Transcriptional and functional profiling of human embryonic stem cell-derived cardiomyocytes. PloS one. 2008;3(10):e3474.
18. Den Hartogh SC, Wolstencroft K, Mummery CL, Passier R. A comprehensive gene expression analysis at sequential stages of in vitro cardiac differentiation from isolated MESP1-expressing-mesoderm progenitors. Scientific reports. 2016;6:19386.
19. Fonoudi H, Yeganeh M, Fattahi F, Ghazizadeh Z, Rassouli H, Alikhani M, et al. ISL1 protein transduction promotes cardiomyocyte differentiation from human embryonic stem cells. PLoS One. 2013;8(1):e55577.
20. Olson EN. Gene regulatory networks in the evolution and development of the heart. Science. 2006;313(5795):1922-7.
21. Akazawa H, Komuro I. Roles of cardiac transcription factors in cardiac hypertrophy. Circulation research. 2003;92(10):1079-88.
22. Dodou E, Verzi MP, Anderson JP, Xu S-M, Black BL. Mef2c is a direct transcriptional target of ISL1 and GATA factors in the anterior heart field during mouse embryonic development. Development. 2004;131(16):3931-42.
23. Munshi NV. Gene regulatory networks in cardiac conduction system development. Circulation research. 2012;110(11):1525-37.