Exosome-Like Vesicles as New Mediators and Therapeutic Targets for Treating Insulin Resistance and β-Cell Mass Failure in Type 2 Diabetes Mellitus.
Qian GeXin Xin XieXiaoqiu XiaoJunli LiuPublished in: Journal of diabetes research (2019)
Exosome-like vesicles (ELVs), the smallest class of extracellular vesicles released from cells, function in cellular crosstalk and therefore profoundly affect physiologic responses and pathologic progression. A growing body of evidence supports a novel role for ELVs as important mediators and therapeutic targets due to their effects on regulation of both insulin signaling and β-cell mass. Pathologic conditions associated with type 2 diabetes (such as high blood glucose, inflammation, hypoxia, and fatty acids) can alter the quantity and components of ELVs secreted from the pancreas or peripheral insulin-targeting tissues. These released ELVs can either enter the blood circulation or be taken up by neighboring cells or macrophages, which can lead to insulin resistance or β-cell apoptosis. This review focuses on the roles of ELVs in insulin resistance and β-cell failure and also highlights the potential use of ELVs and exosome-based delivery systems in therapeutic interventions aimed at treating type 2 diabetes mellitus as well as the challenges associated with exosome-targeting therapeutics.
Keyphrases
- insulin resistance
- glycemic control
- type diabetes
- blood glucose
- single cell
- induced apoptosis
- adipose tissue
- cell therapy
- high fat diet
- metabolic syndrome
- cell cycle arrest
- neoadjuvant chemotherapy
- fatty acid
- gene expression
- blood pressure
- stem cells
- cancer therapy
- endothelial cells
- cell proliferation
- high fat diet induced
- squamous cell carcinoma
- drug delivery
- weight loss
- risk assessment
- pi k akt
- cardiovascular risk factors