Institut de Génomique Fonctionnelle, Université de Montpellier, Centre National de la Recherche Scientifique (CNRS), Institut National de la Santé et de la Recherche Médicale (INSERM), 34094 Montpellier, France.
Université Lille, Centre National de la Recherche Scientifique (CNRS), Centrale Lille, Université Polytechnique Hauts-de-France, UMR 8520, IEMN, F59000 Lille, France.
Cells. 2024 Jul 24;13(15):1244. doi: 10.3390/cells13151244.
Preserving the function and survival of pancreatic beta-cells, in order to achieve long-term glycemic control and prevent complications, is an essential feature for an innovative drug to have clinical value in the treatment of diabetes. Innovative research is developing therapeutic strategies to prevent pathogenic mechanisms and protect beta-cells from the deleterious effects of inflammation and/or chronic hyperglycemia over time. A better understanding of receptors and signaling pathways, and of how they interact with each other in beta-cells, remains crucial and is a prerequisite for any strategy to develop therapeutic tools aimed at modulating beta-cell function and/or mass. Here, we present a comprehensive review of our knowledge on membrane and intracellular receptors and signaling pathways as targets of interest to protect beta-cells from dysfunction and apoptotic death, which opens or could open the way to the development of innovative therapies for diabetes.
为了实现长期血糖控制和预防并发症,保护胰岛β细胞的功能和存活是治疗糖尿病的创新药物具有临床价值的关键特征。创新性研究正在开发治疗策略,以预防致病机制,并防止β细胞随着时间的推移受到炎症和/或慢性高血糖的有害影响。更好地了解受体和信号通路,以及它们在β细胞中相互作用的方式,仍然至关重要,这是开发旨在调节β细胞功能和/或质量的治疗工具的任何策略的前提。在这里,我们全面回顾了我们对膜和细胞内受体以及信号通路的认识,这些受体和信号通路是保护β细胞免受功能障碍和细胞凋亡的目标,这为糖尿病的创新治疗方法的发展开辟了或可能开辟了道路。