» Articles » PMID: 38132306

Exosomes: New Insights into the Pathogenesis of Metabolic Syndrome

Overview
Journal Biology (Basel)
Publisher MDPI
Specialty Biology
Date 2023 Dec 22
PMID 38132306
Authors
Affiliations
Soon will be listed here.
Abstract

Exosomes are a subtype of extracellular vesicles (EVs) with a diameter of 30~150 nm (averaging ~100 nm) that are primarily produced through the endosomal pathway, and carry various components such as lipids, proteins, RNA, and other small molecular substances. Exosomes can mediate intercellular communication through the bioactive substances they carry, thus participating in different physiological activities. Metabolic syndrome (MS) is a disease caused by disturbances in the body's metabolism, mainly including insulin resistance (IR), diabetes, obesity, non-alcoholic fatty liver disease (NAFLD), hyperlipidemia, and atherosclerosis (AS). Recent studies have shown that exosomes are closely related to the occurrence and development of MS. Exosomes can act as messengers to mediate signaling transductions between metabolic cells in the organism and play a bidirectional regulatory role in the MS process. This paper mainly reviews the components, biogenesis, biological functions and potential applications of exosomes, and exosomes involved in the pathogenesis of MS as well as their clinical significance in MS diagnosis.

Citing Articles

Exosomes Derived from Adipose Mesenhymal Stem Cells Ameliorate Lipid Metabolism Disturbances Following Liver Ischemia-Reperfusion Injury in Miniature Swine.

Lu X, Wang Y, Piao C, Li P, Cao L, Liu T Int J Mol Sci. 2024; 25(23).

PMID: 39684778 PMC: 11641803. DOI: 10.3390/ijms252313069.

References
1.
Mori M, Ludwig R, Garcia-Martin R, Brandao B, Kahn C . Extracellular miRNAs: From Biomarkers to Mediators of Physiology and Disease. Cell Metab. 2019; 30(4):656-673. PMC: 6774861. DOI: 10.1016/j.cmet.2019.07.011. View

2.
Buntsma N, van der Pol E, Nieuwland R, Gasecka A . Extracellular Vesicles in Coronary Artery Disease. Adv Exp Med Biol. 2023; 1418:81-103. DOI: 10.1007/978-981-99-1443-2_6. View

3.
Sanchez C, Andahur E, Valenzuela R, Castellon E, Fulla J, Ramos C . Exosomes from bulk and stem cells from human prostate cancer have a differential microRNA content that contributes cooperatively over local and pre-metastatic niche. Oncotarget. 2015; 7(4):3993-4008. PMC: 4826185. DOI: 10.18632/oncotarget.6540. View

4.
Wang Z, Zhang J, Zhang S, Yan S, Wang Z, Wang C . MiR‑30e and miR‑92a are related to atherosclerosis by targeting ABCA1. Mol Med Rep. 2019; 19(4):3298-3304. DOI: 10.3892/mmr.2019.9983. View

5.
Montecalvo A, Larregina A, Shufesky W, Stolz D, Sullivan M, Karlsson J . Mechanism of transfer of functional microRNAs between mouse dendritic cells via exosomes. Blood. 2011; 119(3):756-66. PMC: 3265200. DOI: 10.1182/blood-2011-02-338004. View