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肌醇多磷酸盐对细胞调控的新认识:来自胰腺β细胞的启示。

New horizons in cellular regulation by inositol polyphosphates: insights from the pancreatic β-cell.

机构信息

The Rolf Luft Research Center for Diabetes and Endocrinology, Karolinska Institutet, 171 76 Stockholm, Sweden.

出版信息

Pharmacol Rev. 2013 Feb 19;65(2):641-69. doi: 10.1124/pr.112.006775. Print 2013 Apr.

Abstract

Studies of inositol polyphosphates in the pancreatic β-cell have led to an exciting synergism between new discoveries regarding their cellular roles and new insights into β-cell function. Because the loss or malfunction of the β-cell is central to diabetes, these studies open the possibility of new pharmacological interventions in a disease that has reached epidemic proportions worldwide. Using the β-cell as our prime but not exclusive example, we examine the inositol polyphosphates in three main groups: 1) inositol 1,4,5-trisphosphate and its influence on Ca(2+) signaling, specifically in a cell in which cytoplasmic-free Ca(2+) concentration is principally increased by plasma membrane standing voltage-gated Ca(2+) channels; 2) higher inositol polyphosphates including a novel second messenger inositol 3,4,5,6-tetrakisphosphate and a regulatory role for inositol hexakisphosphate in β-cell Ca(2+) homeostasis and exo- and endocytosis; and 3) inositol pyrophosphates and their role in β-cell exocytosis, together with the exciting possibility of being novel targets for therapy in diabetes. We conclude with some of the new perspectives that are likely to become apparent in the next few years.

摘要

对胰腺β细胞中肌醇多磷酸盐的研究,促成了其细胞功能新发现与β细胞功能新见解之间令人兴奋的协同作用。由于β细胞的缺失或功能失常是糖尿病的核心问题,这些研究为一种在全球范围内呈流行趋势的疾病提供了新的药物干预的可能性。我们将β细胞作为主要但非唯一的范例,在三个主要组别中研究肌醇多磷酸盐:1)肌醇 1,4,5-三磷酸及其对 Ca(2+)信号转导的影响,特别是在细胞质游离 Ca(2+)浓度主要由质膜静息电压门控 Ca(2+)通道增加的细胞中;2)包括新型第二信使肌醇 3,4,5,6-四磷酸在内的较高肌醇多磷酸盐,以及肌醇六磷酸在β细胞 Ca(2+)动态平衡和外排与内吞中的调节作用;3)肌醇焦磷酸盐及其在β细胞胞吐作用中的作用,以及它们成为糖尿病治疗新靶点的令人兴奋的可能性。我们在最后总结了在未来几年可能会变得明显的一些新观点。

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