β-Cell MicroRNAs: Small but Powerful
Open accessAbstract
Noncoding RNA and especially microRNAs (miRs) have emerged as important regulators of key processes in cell biology, including development, differentiation, and survival. Currently, over 2,500 mature miRs have been reported in humans, and considering that each miR has multiple targets, the number of genes and pathways potentially affected is huge. Not surprisingly, many miRs have also been implicated in diabetes, and more recently, some have been discovered to play important roles in the pancreatic islet, including β-cell function, proliferation, and survival. The goal of this Perspective is to offer an overview of this rapidly evolving field and the miRs involved, reveal novel networks of β-cell miR signaling, and provide an outlook of the opportunities and challenges ahead.
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The increase in miR-29 in β-cells exposed to elevated glucose mediates the reduction of glucose-stimulated insulin secretion caused by long-term hypoglycemia via reduced expression of syntaxin-1.
“MiR-29 is increased in β-cells exposed to elevated glucose and it was proposed that this mediates the reduction of glucose-stimulated insulin secretion caused by long-term hypoglycemia via reduced expression of syntaxin-1 (186, 218).”
From Pancreatic β-Cell Electrical Activity and Insulin Secretion: Of Mice and Men (2018) · cites this paper as [186]
In “Insulin Secretion: Preventing Excess” (page not provided), the review says miR-29 increases in response to glucose and that the associated decrease in syntaxin-1 negatively affects glucose-stimulated insulin secretion. It does not attribute that reduction to long-term hypoglycemia; that condition is unsupported. (LLM, conf=0.90)
Experimental — accuracy not yet measuredMiR-29 is increased in β-cells exposed to elevated glucose.
“MiR-29 is increased in β-cells exposed to elevated glucose and it was proposed that this mediates the reduction of glucose-stimulated insulin secretion caused by long-term hypoglycemia via reduced expression of syntaxin-1 (186, 218).”
From Pancreatic β-Cell Electrical Activity and Insulin Secretion: Of Mice and Men (2018) · cites this paper as [186]
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Safdar, A., & Tarnopolsky, M. A. (2018) · Cold Spring Harbor Perspectives in Medicine · doi:10.1101/cshperspect.a029827 · Cited by 203 · see citing works
Ibrahim, S., Johnson, M., Stephens, C. H., Xu, J., Moore, R., Mariani, A., Contreras, C., Syed, F., Mirmira, R. G., Anderson, R. M., et al. (2021) · Molecular Metabolism · doi:10.1016/j.molmet.2021.101289 · Cited by 18 · see citing works
- Authors
- Filios, S. R., & Shalev, A.
- Affiliations
- University of Alabama at Birmingham (US)
- Corresponding author
- Shalev, Anath
- ORCID
- Shalev, Anath
- Venue
- Diabetes
- Publisher
- American Diabetes Association
- Published
- 2015-10-14
- Volume
- 64
- Issue
- 11
- Pages
- 3631-3644
- ISSN
- 0012-1797 (ISSN-L)
- 1939-327X
- PMC
- PMC4613982
- OpenAlex
- W2097687832
- Cited by
- 106
- References
- 7
- Citations by year
- 2026: 1 · 2025: 3 · 2024: 2 · 2023: 7 · 2022: 11 · 2021: 15 · 2020: 13 · 2019: 16 · 2018: 11 · 2017: 15 · 2016: 12
- FWCI
- 2.43
- Type
- journal article
- Language
- en
- Open access
- green
- www.ncbi.nlm.nih.gov
- Locations
- Diabetes (publishedVersion)
- Europe PMC (PubMed Central) (publishedVersion)
- PubMed Central (publishedVersion)
- PubMed (publishedVersion)
- Funders
- National Institutes of Health (R01DK078752)
- Topics
- Health Sciences › Medicine › Surgery › Pancreatic function and diabetes
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Cancer Research › MicroRNA in disease regulation
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Genetics › Diabetes and associated disorders
- Keywords
- microRNA, pancreatic beta cells, beta-cell function, beta-cell proliferation, beta-cell survival, pancreatic islets, non-coding RNA
- MeSH terms
- Cell Differentiation, Cell Survival, Diabetes Mellitus, Humans, Signal Transduction, MicroRNAs, Cell Proliferation, Insulin-Secreting Cells
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