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本文引用的文献

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Comment on Satin et al. "Take Me To Your Leader": An Electrophysiological Appraisal of the Role of Hub Cells in Pancreatic Islets. Diabetes 2020;69:830-836.对萨廷等人《带我去见你的领袖》的评论:胰岛中枢纽细胞作用的电生理评估。《糖尿病》2020年;69卷:830 - 836页
Diabetes. 2020 Sep;69(9):e10-e11. doi: 10.2337/db20-0501.
2
Mechanism and effects of pulsatile GABA secretion from cytosolic pools in the human beta cell.人胰岛β细胞胞浆内囊泡间歇性 GABA 分泌的机制和作用。
Nat Metab. 2019 Nov;1(11):1110-1126. doi: 10.1038/s42255-019-0135-7. Epub 2019 Nov 15.
3
Integrated human pseudoislet system and microfluidic platform demonstrate differences in GPCR signaling in islet cells.集成人拟胰岛系统和微流控平台展示胰岛细胞中 G 蛋白偶联受体信号的差异。
JCI Insight. 2020 May 21;5(10):137017. doi: 10.1172/jci.insight.137017.
4
"Take Me To Your Leader": An Electrophysiological Appraisal of the Role of Hub Cells in Pancreatic Islets.“带我去找你们的首领”:胰岛细胞中腔细胞作用的电生理学评价。
Diabetes. 2020 May;69(5):830-836. doi: 10.2337/dbi19-0012.
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In Vitro Platform for Studying Human Insulin Release Dynamics of Single Pancreatic Islet Microtissues at High Resolution.体外平台用于高分辨率研究单个胰岛微组织的人胰岛素释放动力学。
Adv Biosyst. 2020 Mar;4(3):e1900291. doi: 10.1002/adbi.201900291. Epub 2020 Jan 29.
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Secretory Functions of Macrophages in the Human Pancreatic Islet Are Regulated by Endogenous Purinergic Signaling.巨噬细胞在人胰岛中的分泌功能受内源性嘌呤能信号的调节。
Diabetes. 2020 Jun;69(6):1206-1218. doi: 10.2337/db19-0687. Epub 2020 Apr 3.
7
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Cell. 2020 Mar 19;180(6):1198-1211.e19. doi: 10.1016/j.cell.2020.02.048.
8
The Local Paracrine Actions of the Pancreatic α-Cell.胰腺α细胞的局部旁分泌作用。
Diabetes. 2020 Apr;69(4):550-558. doi: 10.2337/dbi19-0002. Epub 2019 Dec 27.
9
The Role of the Islet Niche on Beta Cell Structure and Function.胰岛微环境对胰岛β细胞结构和功能的作用
J Mol Biol. 2020 Mar 6;432(5):1407-1418. doi: 10.1016/j.jmb.2019.10.032. Epub 2019 Nov 9.
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Nat Methods. 2019 Nov;16(11):1169-1175. doi: 10.1038/s41592-019-0586-5. Epub 2019 Oct 7.

解析协调胰腺胰岛功能的复杂通讯网络。

Deciphering the Complex Communication Networks That Orchestrate Pancreatic Islet Function.

机构信息

Department of Medicine, University of Miami Leonard M. Miller School of Medicine, Miami, FL

Diabetes Research Institute, University of Miami Leonard M. Miller School of Medicine, Miami, FL.

出版信息

Diabetes. 2021 Jan;70(1):17-26. doi: 10.2337/dbi19-0033.

DOI:10.2337/dbi19-0033
PMID:33355306
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7881851/
Abstract

Pancreatic islets are clusters of hormone-secreting endocrine cells that rely on intricate cell-cell communication mechanisms for proper function. The importance of multicellular cooperation in islet cell physiology was first noted nearly 30 years ago in seminal studies showing that hormone secretion from endocrine cell types is diminished when these cells are dispersed. These studies showed that reestablishing cellular contacts in so-called pseudoislets caused endocrine cells to regain hormone secretory function. This not only demonstrated that cooperation between islet cells is highly synergistic but also gave birth to the field of pancreatic islet organoids. Here we review recent advances related to the mechanisms of islet cell cross talk. We first describe new developments that revise current notions about purinergic and GABA signaling in islets. Then we comment on novel multicellular imaging studies that are revealing emergent properties of islet communication networks. We finish by highlighting and discussing recent synthetic approaches that use islet organoids of varied cellular composition to interrogate intraislet signaling mechanisms. This reverse engineering of islets not only will shed light on the mechanisms of intraislet signaling and define communication networks but also may guide efforts aimed at restoring islet function and β-cell mass in diabetes.

摘要

胰岛是一簇分泌激素的内分泌细胞,其正常功能依赖于复杂的细胞间通讯机制。近 30 年前的一些开创性研究首次指出,胰岛细胞的激素分泌会减少,当这些细胞分散时。这些研究表明,在所谓的胰岛拟态中重新建立细胞接触会使内分泌细胞恢复激素分泌功能。这不仅证明了胰岛细胞之间的合作具有高度协同性,而且还催生了胰岛类器官领域。在这里,我们回顾了与胰岛细胞串扰机制相关的最新进展。我们首先描述了修正目前关于胰岛中嘌呤能和 GABA 信号的新进展。然后,我们评论了新的多细胞成像研究,这些研究揭示了胰岛通讯网络的新兴特性。最后,我们强调并讨论了最近使用具有不同细胞组成的胰岛类器官来研究胰岛内信号机制的合成方法。这种胰岛的反向工程不仅将阐明胰岛内信号的机制并定义通讯网络,而且可能为恢复糖尿病中的胰岛功能和β细胞质量的努力提供指导。