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Defining the miRnome of Saphenous Vein Smooth Muscle Cells from Patients with Type 2 Diabetes Mellitus

Hussain, Alisah; Asare-Amankwah, Yaw; Qureshi, Shehryar; Thornton, M. Julie; Palmer, Timothy M.; Bolanle, Israel O; Wood, Ian C.; Turner, Neil A; Porter, Karen E; Tedder, Andrew; Riches-Suman, Kirsten

Authors

Alisah Hussain

Yaw Asare-Amankwah

Shehryar Qureshi

M. Julie Thornton

Israel O Bolanle

Ian C. Wood

Neil A Turner

Karen E Porter

Andrew Tedder

Kirsten Riches-Suman



Abstract

Type 2 diabetes mellitus (T2DM) patients suffer premature development of cardiovascular disease and commonly require cardiac revascularization using the autologous saphenous vein (SV). Smooth muscle cells (SMCs) are the principal cell type within the vascular wall and are dysfunctional in T2DM SV-SMCs, yet the mechanisms underpinning this are incompletely understood. The purpose of this study was to interrogate differential microRNA (miRNA) expression in SV-SMCs to enhance our understanding of T2DM SV-SMC phenotypic change. miRNA expression in primary human SV-SMCs from T2DM and non-diabetic (ND) donors was determined using an array (n = 6 each of ND and T2DM SV-SMCs). Differentially expressed miRNAs were ranked, and functional annotation of the 30 most differentially expressed miRNAs using DAVID and KEGG analysis revealed pathways related to SMC phenotype, including proliferation, migration, cytokine production and cell signaling. After selecting miRNAs known to be involved in SMC phenotypic regulation, miR-17, miR-29b-2, miR-31, miR-130b and miR-491 were further validated using qRT-PCR (n = 5 each of ND and T2DM SV-SMC), with miR-29b-2 subsequently being removed from further investigation. Potential mRNA targets were identified using mirDIP. Predicted target analysis highlighted likely dysregulation in transcription, epigenetic regulation, cell survival, intracellular signaling and cytoskeletal regulation, all of which are known to be dysfunctional in T2DM SV-SMCs. In conclusion, this paper identified four miRNAs that are dysregulated in T2DM SV-SMCs and are implicated in functional changes in the behavior of these cells. This provides a step forward in our understanding of the molecular and epigenetic regulation of vascular dysfunction in T2DM.

Citation

Hussain, A., Asare-Amankwah, Y., Qureshi, S., Thornton, M. J., Palmer, T. M., Bolanle, I. O., Wood, I. C., Turner, N. A., Porter, K. E., Tedder, A., & Riches-Suman, K. (2024). Defining the miRnome of Saphenous Vein Smooth Muscle Cells from Patients with Type 2 Diabetes Mellitus. Diabetology, 5(2), 178-189. https://doi.org/10.3390/diabetology5020014

Journal Article Type Article
Acceptance Date May 10, 2024
Online Publication Date May 11, 2024
Publication Date Jun 1, 2024
Deposit Date May 15, 2024
Publicly Available Date May 17, 2024
Journal Diabetology
Electronic ISSN 2673-4540
Publisher MDPI
Peer Reviewed Peer Reviewed
Volume 5
Issue 2
Pages 178-189
DOI https://doi.org/10.3390/diabetology5020014
Keywords Smooth muscle cell; Type 2 diabetes; Atherosclerosis; Coronary artery bypass graft; MicroRNA
Public URL https://hull-repository.worktribe.com/output/4666892

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Publisher Licence URL
http://creativecommons.org/licenses/by/4.0

Copyright Statement
© 2024 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).





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