• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

最先进的显微镜技术用于研究胰岛:接下来有何期待?

State-of-the-art microscopy to understand islets of Langerhans: what to expect next?

机构信息

Department of Biomedical Sciences of Cells and Systems, University of Groningen, University Medical Center Groningen, Groningen, The Netherlands.

出版信息

Immunol Cell Biol. 2021 May;99(5):509-520. doi: 10.1111/imcb.12450.

DOI:10.1111/imcb.12450
PMID:33667022
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8252556/
Abstract

The discovery of Langerhans and microscopic description of islets in the pancreas were crucial steps in the discovery of insulin. Over the past 150 years, many discoveries in islet biology and type 1 diabetes have been made using powerful microscopic techniques. In the past decade, combination of new probes, animal and tissue models, application of new biosensors and automation of light and electron microscopic methods and other (sub)cellular imaging modalities have proven their potential in understanding the beta cell under (patho)physiological conditions. The imaging evolution, from fluorescent jellyfish to real-time intravital functional imaging, the revolution in automation and data handling and the increased resolving power of analytical imaging techniques are now converging. Here, we review innovative approaches that address islet biology from new angles by studying cells and molecules at high spatiotemporal resolution and in live models. Broad implementation of these cellular imaging techniques will shed new light on cause/consequence of (mal)function in islets of Langerhans in the years to come.

摘要

郎格汉斯和胰腺胰岛的微观描述的发现是胰岛素发现过程中的关键步骤。在过去的 150 年中,使用强大的显微镜技术在胰岛生物学和 1 型糖尿病方面取得了许多发现。在过去的十年中,新型探针的结合、动物和组织模型的应用、新型生物传感器的应用以及光和电子显微镜方法的自动化和其他(亚)细胞成像方式的自动化,已经证明了它们在理解(病理)生理条件下β细胞方面的潜力。从荧光水母到实时活体功能成像的成像演变、自动化和数据处理的革命以及分析成像技术的分辨率的提高正在汇聚。在这里,我们通过研究高时空分辨率和活体模型中的细胞和分子,从新的角度回顾了创新的方法,这些方法可以解决胰岛生物学问题。这些细胞成像技术的广泛应用将在未来几年为胰岛的(功能)失调的因果关系提供新的认识。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9fd3/8252556/c8341f52e0b7/IMCB-99-509-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9fd3/8252556/f7339bacb3ed/IMCB-99-509-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9fd3/8252556/e1d4038d1388/IMCB-99-509-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9fd3/8252556/fec04ac6471d/IMCB-99-509-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9fd3/8252556/c8341f52e0b7/IMCB-99-509-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9fd3/8252556/f7339bacb3ed/IMCB-99-509-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9fd3/8252556/e1d4038d1388/IMCB-99-509-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9fd3/8252556/fec04ac6471d/IMCB-99-509-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9fd3/8252556/c8341f52e0b7/IMCB-99-509-g002.jpg

相似文献

1
State-of-the-art microscopy to understand islets of Langerhans: what to expect next?最先进的显微镜技术用于研究胰岛:接下来有何期待?
Immunol Cell Biol. 2021 May;99(5):509-520. doi: 10.1111/imcb.12450.
2
Experimental approaches for high-resolution in vivo imaging of islet of Langerhans biology.用于活体胰岛生物学高分辨率成像的实验方法。
Curr Diab Rep. 2011 Oct;11(5):420-5. doi: 10.1007/s11892-011-0207-x.
3
A Versatile, Portable Intravital Microscopy Platform for Studying Beta-cell Biology In Vivo.一种用于活体研究β细胞生物学的多功能、便携式活体显微镜平台。
Sci Rep. 2019 Jun 11;9(1):8449. doi: 10.1038/s41598-019-44777-0.
4
Early deficits in insulin secretion, beta cell mass and islet blood perfusion precede onset of autoimmune type 1 diabetes in BioBreeding rats.胰岛素分泌、β细胞质量和胰岛血流灌注的早期缺陷先于 BioBreeding 大鼠自身免疫 1 型糖尿病的发病。
Diabetologia. 2018 Apr;61(4):896-905. doi: 10.1007/s00125-017-4512-z. Epub 2017 Dec 6.
5
[Electron microscopic findings in A-cells of the islands of Langerhans in diabetes mellitus].[糖尿病患者胰岛A细胞的电子显微镜检查结果]
Zentralbl Allg Pathol. 1984;129(4):323-41.
6
In vivo imaging of type 1 diabetes immunopathology using eye-transplanted islets in NOD mice.利用 NOD 小鼠眼移植胰岛对 1 型糖尿病免疫病理学进行体内成像。
Diabetologia. 2019 Jul;62(7):1237-1250. doi: 10.1007/s00125-019-4879-0. Epub 2019 May 14.
7
Distribution of IL-1β immunoreactive cells in pancreatic biopsies from living volunteers with new-onset type 1 diabetes: comparison with donors without diabetes and with longer duration of disease.新发 1 型糖尿病患者活体胰腺活检中 IL-1β 免疫反应细胞的分布:与无糖尿病供体和疾病病程较长者的比较。
Diabetologia. 2018 Jun;61(6):1362-1373. doi: 10.1007/s00125-018-4600-8. Epub 2018 Mar 27.
8
Using Pancreas Tissue Slices for the Study of Islet Physiology.使用胰腺组织切片研究胰岛生理学。
Methods Mol Biol. 2020;2128:301-312. doi: 10.1007/978-1-0716-0385-7_20.
9
Growth and development of the islets of Langerhans: implications for the treatment of diabetes mellitus.胰岛的生长与发育:对糖尿病治疗的启示
Curr Opin Pharmacol. 2001 Dec;1(6):641-50. doi: 10.1016/s1471-4892(01)00109-6.
10
Histology of Type 1 Diabetes Pancreas.1型糖尿病胰腺的组织学
Methods Mol Biol. 2016;1433:105-17. doi: 10.1007/7651_2015_287.

引用本文的文献

1
Multiple sclerosis: what have we learned and can we still learn from electron microscopy.多发性硬化症:我们学到了什么,以及我们还能从电子显微镜中学到什么。
Cell Mol Life Sci. 2025 Apr 23;82(1):172. doi: 10.1007/s00018-025-05690-0.
2
Machine-learning-guided recognition of α and β cells from label-free infrared micrographs of living human islets of Langerhans.基于无标记的活人类胰岛红外显微图像,通过机器学习对 α 和 β 细胞进行识别。
Sci Rep. 2024 Jun 20;14(1):14235. doi: 10.1038/s41598-024-65161-7.
3
Mitochondrial Dynamics and Insulin Secretion.

本文引用的文献

1
Pancreatic beta cell autophagy is impaired in type 1 diabetes.1 型糖尿病中胰腺β细胞自噬受损。
Diabetologia. 2021 Apr;64(4):865-877. doi: 10.1007/s00125-021-05387-6. Epub 2021 Jan 30.
2
Image-Based Machine Learning Algorithms for Disease Characterization in the Human Type 1 Diabetes Pancreas.基于图像的机器学习算法在人类 1 型糖尿病胰腺疾病特征中的应用。
Am J Pathol. 2021 Mar;191(3):454-462. doi: 10.1016/j.ajpath.2020.11.010. Epub 2020 Dec 8.
3
Pancreatlas: Applying an Adaptable Framework to Map the Human Pancreas in Health and Disease.
线粒体动态与胰岛素分泌。
Int J Mol Sci. 2023 Sep 7;24(18):13782. doi: 10.3390/ijms241813782.
4
Scanning electron microscopy of human islet cilia.人胰岛纤毛的扫描电子显微镜观察。
Proc Natl Acad Sci U S A. 2023 May 30;120(22):e2302624120. doi: 10.1073/pnas.2302624120. Epub 2023 May 19.
5
Single-cell RNA-seq transcriptomic landscape of human and mouse islets and pathological alterations of diabetes.人类和小鼠胰岛的单细胞RNA测序转录组图谱及糖尿病的病理改变
iScience. 2022 Oct 14;25(11):105366. doi: 10.1016/j.isci.2022.105366. eCollection 2022 Nov 18.
胰腺图谱:应用适应性框架绘制健康与疾病状态下的人类胰腺图谱。
Patterns (N Y). 2020 Oct 5;1(8):100120. doi: 10.1016/j.patter.2020.100120. eCollection 2020 Nov 13.
4
Determination of secretory granule maturation times in pancreatic islet β-cells by serial block-face electron microscopy.通过连续块面电子显微镜确定胰岛 β 细胞分泌颗粒的成熟时间。
J Struct Biol. 2020 Oct 1;212(1):107584. doi: 10.1016/j.jsb.2020.107584. Epub 2020 Jul 28.
5
Leader β-cells coordinate Ca dynamics across pancreatic islets in vivo.胰岛内的β细胞负责人体的钙动力学的协调。
Nat Metab. 2019 Jun;1(6):615-629. doi: 10.1038/s42255-019-0075-2. Epub 2019 Jun 14.
6
ZIGIR, a Granule-Specific Zn Indicator, Reveals Human Islet α Cell Heterogeneity.ZIGIR,一种颗粒特异性锌指示剂,揭示了人类胰岛 α 细胞的异质性。
Cell Rep. 2020 Jul 14;32(2):107904. doi: 10.1016/j.celrep.2020.107904.
7
Long-term culture of human pancreatic slices as a model to study real-time islet regeneration.长期培养的人胰腺切片作为研究实时胰岛再生的模型。
Nat Commun. 2020 Jun 29;11(1):3265. doi: 10.1038/s41467-020-17040-8.
8
Longitudinal In Vivo Imaging and Quantification of Human Pancreatic Islet Grafting and Contributing Host Cells in the Anterior Eye Chamber.人胰岛移植及前房内供体宿主细胞的纵向体内成像与定量分析
J Vis Exp. 2020 Jun 11(160). doi: 10.3791/61234.
9
Large-scale electron microscopy database for human type 1 diabetes.人类 1 型糖尿病的大规模电子显微镜数据库。
Nat Commun. 2020 May 18;11(1):2475. doi: 10.1038/s41467-020-16287-5.
10
Super-resolution microscopy compatible fluorescent probes reveal endogenous glucagon-like peptide-1 receptor distribution and dynamics.超分辨率显微镜兼容的荧光探针揭示内源性胰高血糖素样肽-1 受体的分布和动态。
Nat Commun. 2020 Jan 24;11(1):467. doi: 10.1038/s41467-020-14309-w.