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2型糖尿病发生发展过程中的器官间串扰。

Inter-organ crosstalk during development and progression of type 2 diabetes mellitus.

作者信息

Xourafa Georgia, Korbmacher Melis, Roden Michael

机构信息

Institute for Clinical Diabetology, German Diabetes Center, Leibniz Center for Diabetes Research at Heinrich-Heine-University Düsseldorf, Düsseldorf, Germany.

German Center for Diabetes Research, Partner Düsseldorf, München-Neuherberg, Düsseldorf, Germany.

出版信息

Nat Rev Endocrinol. 2024 Jan;20(1):27-49. doi: 10.1038/s41574-023-00898-1. Epub 2023 Oct 16.


DOI:10.1038/s41574-023-00898-1
PMID:37845351
Abstract

Type 2 diabetes mellitus (T2DM) is characterized by tissue-specific insulin resistance and pancreatic β-cell dysfunction, which result from the interplay of local abnormalities within different tissues and systemic dysregulation of tissue crosstalk. The main local mechanisms comprise metabolic (lipid) signalling, altered mitochondrial metabolism with oxidative stress, endoplasmic reticulum stress and local inflammation. While the role of endocrine dysregulation in T2DM pathogenesis is well established, other forms of inter-organ crosstalk deserve closer investigation to better understand the multifactorial transition from normoglycaemia to hyperglycaemia. This narrative Review addresses the impact of certain tissue-specific messenger systems, such as metabolites, peptides and proteins and microRNAs, their secretion patterns and possible alternative transport mechanisms, such as extracellular vesicles (exosomes). The focus is on the effects of these messengers on distant organs during the development of T2DM and progression to its complications. Starting from the adipose tissue as a major organ relevant to T2DM pathophysiology, the discussion is expanded to other key tissues, such as skeletal muscle, liver, the endocrine pancreas and the intestine. Subsequently, this Review also sheds light on the potential of multimarker panels derived from these biomarkers and related multi-omics for the prediction of risk and progression of T2DM, novel diabetes mellitus subtypes and/or endotypes and T2DM-related complications.

摘要

2型糖尿病(T2DM)的特征是组织特异性胰岛素抵抗和胰腺β细胞功能障碍,这是由不同组织内的局部异常相互作用以及组织间串扰的全身失调所致。主要的局部机制包括代谢(脂质)信号传导、伴有氧化应激的线粒体代谢改变、内质网应激和局部炎症。虽然内分泌失调在T2DM发病机制中的作用已得到充分证实,但其他形式的器官间串扰值得更深入研究,以便更好地理解从正常血糖到高血糖的多因素转变。本叙述性综述探讨了某些组织特异性信使系统的影响,如代谢物、肽和蛋白质以及微小RNA,它们的分泌模式和可能的替代转运机制,如细胞外囊泡(外泌体)。重点是这些信使在T2DM发展过程中对远处器官的影响以及向其并发症的进展。从作为与T2DM病理生理学相关的主要器官的脂肪组织开始,讨论扩展到其他关键组织,如骨骼肌、肝脏、内分泌胰腺和肠道。随后,本综述还阐明了源自这些生物标志物的多标志物组合以及相关多组学在预测T2DM风险和进展、新型糖尿病亚型和/或内型以及T2DM相关并发症方面的潜力。

相似文献

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Inter-organ crosstalk during development and progression of type 2 diabetes mellitus.

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[3]
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[4]
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[5]
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Immun Inflamm Dis. 2025-8

[6]
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Diabetologia. 2025-8-6

[7]
The Effects of Adipose Tissue Dysregulation on Type 2 Diabetes Mellitus.

Biomedicines. 2025-7-19

[8]
UCP2 inhibition eliminates pancreatic β cell autoinflammation in T2DM with islet-mitochondrial sequential targeting nanomedicines.

Nat Commun. 2025-7-24

[9]
Prediabetes.

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[10]
Genetic regulation of exosome biogenesis pathway in human adipose and muscle tissue and association with obesity and insulin resistance.

Res Sq. 2025-7-11

本文引用的文献

[1]
Reply: A multi-society Delphi consensus statement on new fatty liver disease nomenclature.

Hepatology. 2024-3-1

[2]
Biomarkers to Guide Medical Therapy in Primary Aldosteronism.

Endocr Rev. 2024-1-4

[3]
GDF15 promotes weight loss by enhancing energy expenditure in muscle.

Nature. 2023-7

[4]
Targeting protein modifications in metabolic diseases: molecular mechanisms and targeted therapies.

Signal Transduct Target Ther. 2023-5-27

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Association of osteocalcin, osteoprotegerin, and osteopontin with cardiovascular disease and retinopathy in type 2 diabetes.

Diabetes Metab Res Rev. 2023-7

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Data-driven subgroups of prediabetes and the associations with outcomes in Chinese adults.

Cell Rep Med. 2023-3-21

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Diabetologia. 2023-5

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Proc Natl Acad Sci U S A. 2023-2-14

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Cell Metab. 2023-2-7

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BMC Med. 2023-2-3

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