The role of exosome derived miRNAs in inter-cell crosstalk among insulin-related organs in type 2 diabetes mellitus.
Ting LuYing ZhengXiaoling ChenZhiyong LinChaoqi LiuChengfu YuanPublished in: Journal of physiology and biochemistry (2024)
Exosomes are small extracellular vesicles secreted by almost all cell types, and carry diverse cargo including RNA, and other substances. Recent studies have focused exosomal microRNAs (miRNAs) on various human diseases, including type 2 diabetes mellitus (T2DM) and metabolic syndrome (METS) which accompany the occurrence of insulin resistance. The regulation of insulin signaling has connected with some miRNA expression which play a significant regulatory character in insulin targeted cells or organs, such as fat, muscle, and liver. The miRNAs carried by exosomes, through the circulation in the body fluids, mediate all kinds of physiological and pathological process involved in the human body. Studies have found that exosome derived miRNAs are abnormally expressed and cross-talked with insulin targeted cells or organs to affect insulin pathways. Further investigations of the mechanisms of exosomal miRNAs in T2DM will be valuable for the diagnostic biomarkers and therapeutic targets of T2DM. This review will summarize the molecular mechanism of action of the miRNAs carried by exosomes which are secreted from insulin signaling related cells, and elucidate the pathogenesis of insulin resistance to provide a new strategy for the potential diagnostic biomarkers and therapeutic targets for the type 2 diabetes.
Keyphrases
- type diabetes
- glycemic control
- insulin resistance
- induced apoptosis
- metabolic syndrome
- mesenchymal stem cells
- cell cycle arrest
- stem cells
- adipose tissue
- skeletal muscle
- endothelial cells
- high fat diet
- cardiovascular disease
- weight loss
- single cell
- risk assessment
- induced pluripotent stem cells
- cell therapy
- endoplasmic reticulum stress
- polycystic ovary syndrome
- cancer therapy
- cell death
- cardiovascular risk factors
- oxidative stress
- drinking water
- transcription factor
- uric acid
- drug induced