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β细胞衍生的细胞外囊泡:1型糖尿病胰岛微环境中细胞间通讯的介质

Beta-Cell-Derived Extracellular Vesicles: Mediators of Intercellular Communication in the Islet Microenvironment in Type 1 Diabetes.

作者信息

Dekkers Mette C, Pu Xudong, Enciso-Martinez Agustin, Zaldumbide Arnaud

机构信息

Department of Cell and Chemical Biology, Leiden University Medical Center, 2333 ZA Leiden, The Netherlands.

Oncode Institute, 3521 AL Utrecht, The Netherlands.

出版信息

Cells. 2024 Dec 3;13(23):1996. doi: 10.3390/cells13231996.


DOI:10.3390/cells13231996
PMID:39682744
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11640590/
Abstract

Type 1 diabetes (T1D) is a chronic autoimmune disorder characterised by an autoimmune response specifically mounted against the insulin-producing beta cells. Within the islet, high cellular connectivity and extensive vascularisation facilitate intra-islet communication and direct crosstalk with the surrounding tissues and the immune system. During the development of T1D, cytokines and extracellular vesicles released by beta cells can contribute to the recruitment of immune cells, further amplifying autoimmunity and aggravating beta cell damage and dysfunction. In this review, we will evaluate the role of beta-cell-derived extracellular vesicles as mediators of the autoimmune response and discuss their potential for early diagnosis and new therapeutic strategies in T1D.

摘要

1型糖尿病(T1D)是一种慢性自身免疫性疾病,其特征是针对产生胰岛素的β细胞产生特异性自身免疫反应。在胰岛内,高度的细胞连接性和广泛的血管化促进了胰岛内的通讯以及与周围组织和免疫系统的直接相互作用。在T1D的发展过程中,β细胞释放的细胞因子和细胞外囊泡可促进免疫细胞的募集,进一步放大自身免疫并加重β细胞损伤和功能障碍。在这篇综述中,我们将评估β细胞衍生的细胞外囊泡作为自身免疫反应介质的作用,并讨论它们在T1D早期诊断和新治疗策略中的潜力。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/025b/11640590/6a56cd73a85b/cells-13-01996-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/025b/11640590/94aae7112f22/cells-13-01996-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/025b/11640590/6a56cd73a85b/cells-13-01996-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/025b/11640590/94aae7112f22/cells-13-01996-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/025b/11640590/6a56cd73a85b/cells-13-01996-g002.jpg

相似文献

[1]
Beta-Cell-Derived Extracellular Vesicles: Mediators of Intercellular Communication in the Islet Microenvironment in Type 1 Diabetes.

Cells. 2024-12-3

[2]
Extracellular vesicles derived from stressed beta cells mediate monocyte activation and contribute to islet inflammation.

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[3]
Extracellular Vesicles in Immune System Regulation and Type 1 Diabetes: Cell-to-Cell Communication Mediators, Disease Biomarkers, and Promising Therapeutic Tools.

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[4]
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[5]
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Antioxid Redox Signal. 2022-4

[6]
Extracellular Vesicles in Type 1 Diabetes: Messengers and Regulators.

Curr Diab Rep. 2019-7-31

[7]
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Diabetologia. 2020-3

[8]
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Diabetes Obes Metab. 2017-9

[9]
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Elife. 2025-4-15

[10]
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Front Endocrinol (Lausanne). 2024

引用本文的文献

[1]
Interplay of hypoxia, immune dysregulation, and metabolic stress in pathophysiology of type 1 diabetes.

Front Immunol. 2025-6-4

本文引用的文献

[1]
Beta cell extracellular vesicle PD-L1 as a novel regulator of CD8 T cell activity and biomarker during the evolution of type 1 diabetes.

Diabetologia. 2025-2

[2]
Extracellular vesicles derived from stressed beta cells mediate monocyte activation and contribute to islet inflammation.

Front Immunol. 2024-7-24

[3]
Dual role of autoantibodies to heat shock proteins in autoimmune diseases.

Front Immunol. 2024

[4]
Bioengineered Artificial Extracellular Vesicles Presenting PD-L1 and Gal-9 Ameliorate New-Onset Type 1 Diabetes.

Diabetes. 2024-8-1

[5]
Interactions between the Exocrine and the Endocrine Pancreas.

J Clin Med. 2024-2-19

[6]
Pancreatic β cell derived extracellular vesicles containing surface preproinsulin are involved in glucose stimulated insulin secretion.

Life Sci. 2024-3-1

[7]
A proteomic meta-analysis refinement of plasma extracellular vesicles.

Sci Data. 2023-11-28

[8]
Systematic review of type 1 diabetes biomarkers reveals regulation in circulating proteins related to complement, lipid metabolism, and immune response.

Clin Proteomics. 2023-9-21

[9]
Diabetes as a consequence of acute pancreatitis.

World J Gastroenterol. 2023-8-21

[10]
Immune engineered extracellular vesicles to modulate T cell activation in the context of type 1 diabetes.

Sci Adv. 2023-6-2

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