The small RNA miR-375 - a pancreatic islet abundant miRNA with multiple roles in endocrine beta cell function
(2017) In Molecular and Cellular Endocrinology 456. p.95-101- Abstract
The pathophysiology of diabetes is complex and recent research put focus on the pancreatic islets of Langerhans and the insulin-secreting beta cells as central in the development of the disease. MicroRNAs (miRNAs), the small non-coding RNAs regulating post-transcriptional gene expression, are significant regulators of beta cell function. One of the most abundant miRNAs in the islets is miR-375. This review focus on the role of miR-375 in beta cell function, including effects in development and differentiation, proliferation and regulation of insulin secretion. It also discusses the regulation of miR-375 expression, miR-375 as a potential circulating biomarker in type 1 and type 2 diabetes, and the need for the beta cell to keep... (More)
The pathophysiology of diabetes is complex and recent research put focus on the pancreatic islets of Langerhans and the insulin-secreting beta cells as central in the development of the disease. MicroRNAs (miRNAs), the small non-coding RNAs regulating post-transcriptional gene expression, are significant regulators of beta cell function. One of the most abundant miRNAs in the islets is miR-375. This review focus on the role of miR-375 in beta cell function, including effects in development and differentiation, proliferation and regulation of insulin secretion. It also discusses the regulation of miR-375 expression, miR-375 as a potential circulating biomarker in type 1 and type 2 diabetes, and the need for the beta cell to keep expression of miR-375 within optimal levels. The summed picture of miR-375 is a miRNA with multiple functions with importance in the formation of beta cell identity, control of beta cell mass and regulation of insulin secretion.
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- author
- Eliasson, Lena LU
- organization
- publishing date
- 2017-02-27
- type
- Contribution to journal
- publication status
- published
- subject
- keywords
- Beta cell, Diabetes, Differentiation, Insulin, Insulin secretion, Islet of langerhans, MicroRNA, MiR-375, Proliferation
- in
- Molecular and Cellular Endocrinology
- volume
- 456
- pages
- 95 - 101
- publisher
- Elsevier
- external identifiers
-
- pmid:28254488
- wos:000412250600011
- scopus:85014520847
- ISSN
- 0303-7207
- DOI
- 10.1016/j.mce.2017.02.043
- language
- English
- LU publication?
- yes
- id
- 175260eb-46fd-4a8b-a940-ce7ddc02b1a6
- date added to LUP
- 2017-03-15 12:09:46
- date last changed
- 2025-01-07 09:40:00
@article{175260eb-46fd-4a8b-a940-ce7ddc02b1a6, abstract = {{<p>The pathophysiology of diabetes is complex and recent research put focus on the pancreatic islets of Langerhans and the insulin-secreting beta cells as central in the development of the disease. MicroRNAs (miRNAs), the small non-coding RNAs regulating post-transcriptional gene expression, are significant regulators of beta cell function. One of the most abundant miRNAs in the islets is miR-375. This review focus on the role of miR-375 in beta cell function, including effects in development and differentiation, proliferation and regulation of insulin secretion. It also discusses the regulation of miR-375 expression, miR-375 as a potential circulating biomarker in type 1 and type 2 diabetes, and the need for the beta cell to keep expression of miR-375 within optimal levels. The summed picture of miR-375 is a miRNA with multiple functions with importance in the formation of beta cell identity, control of beta cell mass and regulation of insulin secretion.</p>}}, author = {{Eliasson, Lena}}, issn = {{0303-7207}}, keywords = {{Beta cell; Diabetes; Differentiation; Insulin; Insulin secretion; Islet of langerhans; MicroRNA; MiR-375; Proliferation}}, language = {{eng}}, month = {{02}}, pages = {{95--101}}, publisher = {{Elsevier}}, series = {{Molecular and Cellular Endocrinology}}, title = {{The small RNA miR-375 - a pancreatic islet abundant miRNA with multiple roles in endocrine beta cell function}}, url = {{http://dx.doi.org/10.1016/j.mce.2017.02.043}}, doi = {{10.1016/j.mce.2017.02.043}}, volume = {{456}}, year = {{2017}}, }