Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
Review
. 2017 Jan;28(1):3-18.
doi: 10.1016/j.tem.2016.10.003. Epub 2016 Oct 31.

Extracellular Vesicles: Novel Mediators of Cell Communication In Metabolic Disease

Affiliations
Review

Extracellular Vesicles: Novel Mediators of Cell Communication In Metabolic Disease

Isabel Huang-Doran et al. Trends Endocrinol Metab. 2017 Jan.

Abstract

Metabolic homeostasis emerges from the complex, multidirectional crosstalk between key metabolic tissues including adipose tissue, liver, and skeletal muscle. This crosstalk, traditionally mediated by hormones and metabolites, becomes dysregulated in human diseases such as obesity and diabetes. Extracellular vesicles (EVs; including exosomes) are circulating, cell-derived nanoparticles containing proteins and nucleic acids that interact with and modify local and distant cellular targets. Accumulating evidence, reviewed herein, supports a role for extracellular vesicles in obesity-associated metabolic disturbance, particularly the local and systemic inflammation characteristic of adipose and hepatic stress. As the practical and conceptual challenges facing the field are tackled, this emerging and versatile mode of intercellular communication may afford valuable insights and therapeutic opportunities in combatting these major threats to modern human health.

Keywords: diabetes; exosome; miRNA; nanoparticle; obesity.

PubMed Disclaimer

Publication types

LinkOut - more resources