دورية أكاديمية

KSRP improves pancreatic beta cell function and survival

التفاصيل البيبلوغرافية
العنوان: KSRP improves pancreatic beta cell function and survival
المؤلفون: Leticia Barssotti, Gabriela Moreira Soares, Emílio Marconato-Júnior, Bruna Lourençoni Alves, Kênia Moreno Oliveira, Everardo Magalhães Carneiro, Antonio Carlos Boschero, Helena Cristina Lima Barbosa
المصدر: Scientific Reports, Vol 14, Iss 1, Pp 1-12 (2024)
بيانات النشر: Nature Portfolio, 2024.
سنة النشر: 2024
المجموعة: LCC:Medicine
LCC:Science
مصطلحات موضوعية: KSRP, Pancreatic beta cell, Insulin secretion, Cell death, ER stress, Medicine, Science
الوصف: Abstract Impaired insulin production and/or secretion by pancreatic beta cells can lead to high blood glucose levels and type 2 diabetes (T2D). Therefore, investigating new proteins involved in beta cell response to stress conditions could be useful in finding new targets for therapeutic approaches. KH-type splicing regulatory protein (KSRP) is a protein usually involved in gene expression due to its role in post-transcriptional regulation. Although there are studies describing the important role of KSRP in tissues closely related to glucose homeostasis, its effect on pancreatic beta cells has not been explored so far. Pancreatic islets from diet-induced obese mice (C57BL/6JUnib) were used to determine KSRP expression and we also performed in vitro experiments exposing INS-1E cells (pancreatic beta cell line) to different stressors (palmitate or cyclopiazonic acid—CPA) to induce cellular dysfunction. Here we show that KSRP expression is reduced in all the beta cell dysfunction models tested. In addition, when manipulated to knock down KSRP, beta cells exhibited increased death and impaired insulin secretion, whereas KSRP overexpression prevented cell death and increased insulin secretion. Taken together, our findings suggest that KSRP could be an important target to protect beta cells from impaired functioning and death.
نوع الوثيقة: article
وصف الملف: electronic resource
اللغة: English
تدمد: 2045-2322
العلاقة: https://doaj.org/toc/2045-2322Test
DOI: 10.1038/s41598-024-55505-8
الوصول الحر: https://doaj.org/article/a7b8de6854c84b849cecff4ca428b8ebTest
رقم الانضمام: edsdoj.7b8de6854c84b849cecff4ca428b8eb
قاعدة البيانات: Directory of Open Access Journals
الوصف
تدمد:20452322
DOI:10.1038/s41598-024-55505-8