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
. 2020 Feb 4;17(3):944.
doi: 10.3390/ijerph17030944.

Stem Cell-Derived Exosomes in Autism Spectrum Disorder

Affiliations
Review

Stem Cell-Derived Exosomes in Autism Spectrum Disorder

Nicola Alessio et al. Int J Environ Res Public Health. .

Abstract

Neurodevelopmental lifelong pathologies defined by problems with social interaction, communication capacity and presence of repetitive/stereotyped clusters of behavior and interests are grouped under the definition of autism spectrum disorder (ASD). ASD prevalence is still increasing, indicating the need to identify specific biomarkers and novel pharmacotherapies. Neuroinflammation and neuro-immune cross-talk dysregulation are specific hallmarks of ASD, offering the possibility of treating these disorders by stem cell therapy. Indeed, cellular strategies have been postulated, proposed and applied to ASD. However, less is known about the molecular action mechanisms of stem cells. As a possibility, the positive and restorative effects mediated by stem cells could be due to their paracrine activity, by which stem cells produce and release several ameliorative and anti-inflammatory molecules. Among the secreted complex tools, exosomes are sub-organelles, enriched by RNA and proteins, that provide cell-to-cell communication. Exosomes could be the mediators of many stem cell-associated therapeutic activities. This review article describes the potential role of exosomes in alleviating ASD symptoms.

Keywords: autism spectrum disorder; exosomes; neuroinflammation; stem cells; translational approach.

PubMed Disclaimer

Conflict of interest statement

The authors declare no conflict of interest.

References

    1. Johnstone R.M., Adam M., Hammond J.R., Orr L., Turbide C. Vesicle formation during reticulocyte maturation. Association of plasma membrane activities with released vesicles (exosomes) J. Biol. Chem. 1987;262:9412–9420. - PubMed
    1. Pedro A. The Definition of Exosome and Extracellular Vesicles (EV) Qeios Ltd.; London, UK: 2019.
    1. Borges F.T., Reis L.A., Schor N. Extracellular vesicles: Structure, function, and potential clinical uses in renal diseases. Braz. J. Med Biol. Res. 2013;46:824–830. doi: 10.1590/1414-431X20132964. - DOI - PMC - PubMed
    1. Thery C., Witwer K.W., Aikawa E., Alcaraz M.J., Anderson J.D., Andriantsitohaina R., Antoniou A., Arab T., Archer F., Atkin-Smith G.K., et al. Minimal information for studies of extracellular vesicles 2018 (MISEV2018): A position statement of the International Society for Extracellular Vesicles and update of the MISEV2014 guidelines. J. Extracell. Vesicles. 2018;7:1535750. doi: 10.1080/20013078.2018.1535750. - DOI - PMC - PubMed
    1. Witasp E., Uthaisang W., Elenstrom-Magnusson C., Hanayama R., Tanaka M., Nagata S., Orrenius S., Fadeel B. Bridge over troubled water: Milk fat globule epidermal growth factor 8 promotes human monocyte-derived macrophage clearance of non-blebbing phosphatidylserine-positive target cells. Cell Death Differ. 2007;14:1063–1065. doi: 10.1038/sj.cdd.4402096. - DOI - PubMed