MicroRNA-143 modulates the expression of Natriuretic Peptide Receptor 3 in cardiac cells

Abstract Natriuretic Peptide Receptor 3 (NPR3), the clearance receptor for extracellular bio-active natriuretic peptides (NPs), plays important roles in the homeostasis of body fluid volume and vascular tone. Using luciferase reporter and antagomir-based silencing assays, we demonstrated that the ex...

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Autores principales: Juan Wang, Kai Sing Tong, Lee Lee Wong, Oi-Wah Liew, Divya Raghuram, Arthur Mark Richards, Yei-Tsung Chen
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Publicado: Nature Portfolio 2018
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Acceso en línea:https://doaj.org/article/67a2a64447b84e3bb8fff82915af503b
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spelling oai:doaj.org-article:67a2a64447b84e3bb8fff82915af503b2021-12-02T12:32:47ZMicroRNA-143 modulates the expression of Natriuretic Peptide Receptor 3 in cardiac cells10.1038/s41598-018-25489-32045-2322https://doaj.org/article/67a2a64447b84e3bb8fff82915af503b2018-05-01T00:00:00Zhttps://doi.org/10.1038/s41598-018-25489-3https://doaj.org/toc/2045-2322Abstract Natriuretic Peptide Receptor 3 (NPR3), the clearance receptor for extracellular bio-active natriuretic peptides (NPs), plays important roles in the homeostasis of body fluid volume and vascular tone. Using luciferase reporter and antagomir-based silencing assays, we demonstrated that the expression of NPR3 could be modulated by microRNA-143 (miR-143-3p), a microRNA species with up-regulated circulating concentrations in clinical heart failure. The regulatory effect of miR-143 on NPR3 expression was further evidenced by the reciprocal relationship between miR-143 and NPR3 levels observed in hypoxia-treated human cardiac cells and in left ventricular tissue from rats undergoing experimental myocardial infarction. Further analysis indicated elevation of miR-143 in response to hypoxic challenge reflects transcriptional activation of the miR-143 host gene (MIR143HG). This was corroborated by demonstration of the induction of host gene promoter activity upon hypoxic challenge. Moreover, miR-143 was shown to enhance its own expression by increasing MIR143HG promoter activity, as well as targeting the expressions of NPPA, NPPC, NR3C2, and CRHR2 in cardiac cells. Taken together, these findings suggest that the elevation of miR-143 upon hypoxic insult may be part of a microRNA-based feed forward loop that results in fine tuning the levels of NPs and neurohormonal receptors in cardiac cell lineages.Juan WangKai Sing TongLee Lee WongOi-Wah LiewDivya RaghuramArthur Mark RichardsYei-Tsung ChenNature PortfolioarticleMedicineRScienceQENScientific Reports, Vol 8, Iss 1, Pp 1-11 (2018)
institution DOAJ
collection DOAJ
language EN
topic Medicine
R
Science
Q
spellingShingle Medicine
R
Science
Q
Juan Wang
Kai Sing Tong
Lee Lee Wong
Oi-Wah Liew
Divya Raghuram
Arthur Mark Richards
Yei-Tsung Chen
MicroRNA-143 modulates the expression of Natriuretic Peptide Receptor 3 in cardiac cells
description Abstract Natriuretic Peptide Receptor 3 (NPR3), the clearance receptor for extracellular bio-active natriuretic peptides (NPs), plays important roles in the homeostasis of body fluid volume and vascular tone. Using luciferase reporter and antagomir-based silencing assays, we demonstrated that the expression of NPR3 could be modulated by microRNA-143 (miR-143-3p), a microRNA species with up-regulated circulating concentrations in clinical heart failure. The regulatory effect of miR-143 on NPR3 expression was further evidenced by the reciprocal relationship between miR-143 and NPR3 levels observed in hypoxia-treated human cardiac cells and in left ventricular tissue from rats undergoing experimental myocardial infarction. Further analysis indicated elevation of miR-143 in response to hypoxic challenge reflects transcriptional activation of the miR-143 host gene (MIR143HG). This was corroborated by demonstration of the induction of host gene promoter activity upon hypoxic challenge. Moreover, miR-143 was shown to enhance its own expression by increasing MIR143HG promoter activity, as well as targeting the expressions of NPPA, NPPC, NR3C2, and CRHR2 in cardiac cells. Taken together, these findings suggest that the elevation of miR-143 upon hypoxic insult may be part of a microRNA-based feed forward loop that results in fine tuning the levels of NPs and neurohormonal receptors in cardiac cell lineages.
format article
author Juan Wang
Kai Sing Tong
Lee Lee Wong
Oi-Wah Liew
Divya Raghuram
Arthur Mark Richards
Yei-Tsung Chen
author_facet Juan Wang
Kai Sing Tong
Lee Lee Wong
Oi-Wah Liew
Divya Raghuram
Arthur Mark Richards
Yei-Tsung Chen
author_sort Juan Wang
title MicroRNA-143 modulates the expression of Natriuretic Peptide Receptor 3 in cardiac cells
title_short MicroRNA-143 modulates the expression of Natriuretic Peptide Receptor 3 in cardiac cells
title_full MicroRNA-143 modulates the expression of Natriuretic Peptide Receptor 3 in cardiac cells
title_fullStr MicroRNA-143 modulates the expression of Natriuretic Peptide Receptor 3 in cardiac cells
title_full_unstemmed MicroRNA-143 modulates the expression of Natriuretic Peptide Receptor 3 in cardiac cells
title_sort microrna-143 modulates the expression of natriuretic peptide receptor 3 in cardiac cells
publisher Nature Portfolio
publishDate 2018
url https://doaj.org/article/67a2a64447b84e3bb8fff82915af503b
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