Evidence map›Paper›PMID 31775160›Full record

ArticleNeuropsychopharmacology : official publication of the American College of Neuropsychopharmacology2020

Exosomal secretion of a psychosis-altered miRNA that regulates glutamate receptor expression is affected by antipsychotics.

Stephen K Amoah, Brian A Rodriguez, Constantine N Logothetis, Praveen Chander, Carl M Sellgren, Jason P Weick, Steven D Sheridan, Lauren L Jantzie, Maree J Webster, Nikolaos Mellios

Open access · hybridAbstract read
In one paragraph

Article in Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 48 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
48citing papers in PubMed, 1 pooled it
2.8field-weighted citation impact, top 8% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

48 citing papers in PubMed, 1 synthesis or guideline pooled it, 90 citations in OpenAlex.

  1. Pooled it
  2. Review
  3. Article
  4. Review
  5. Article
  6. Alpha psychiatry · 2026
    Article
  7. Review
  8. MicroRNAs as biomarkers and molecular mediators of cognitive dysfunction in schizophrenia.Journal of neural transmission (Vienna, Austria : 1996) · 2026
    Review
  9. Article
  10. Review
  11. Review
  12. Review
  13. LncRNA-miRNA‒mRNA Network in Schizophrenia.Journal of molecular neuroscience : MN · 2025
    Article
  14. Review
  15. Review
  16. Review
  17. Review
  18. Beyond the Bubble: A Debate on microRNA Sorting Into Extracellular Vesicles.Laboratory investigation; a journal of technical methods and pathology · 2025
    Review
  19. Review
  20. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

10 authors at 5 institutions in 2 countries.

Stephen K AmoahDepartment of Neurosciences, University of New Mexico School of Medicine, Albuquerque, NM, USA.ORCID http://orcid.org/0000-0001-5486-6027
Brian A RodriguezDepartment of Neurosciences, University of New Mexico School of Medicine, Albuquerque, NM, USA.
Constantine N LogothetisDepartment of Neurosciences, University of New Mexico School of Medicine, Albuquerque, NM, USA.
Praveen ChanderDepartment of Neurosciences, University of New Mexico School of Medicine, Albuquerque, NM, USA.
Carl M SellgrenDepartment of Physiology and Pharmacology, Karolinska Institutet, Stockholm, Sweden.
Jason P WeickDepartment of Neurosciences, University of New Mexico School of Medicine, Albuquerque, NM, USA.
Steven D SheridanCenter for Genomic Medicine, Chemical Neurobiology Laboratory, Departments of Neurology and Psychiatry, Massachusetts General Hospital and Harvard Medical School, Boston, MA, USA.
Lauren L JantzieDepartment of Pediatrics, Johns Hopkins School of Medicine, Baltimore, MD, USA.
Maree J WebsterLaboratory of Brain Research, Stanley Medical Research Institute, Chevy Chase, MD, USA.
Nikolaos MelliosDepartment of Neurosciences, University of New Mexico School of Medicine, Albuquerque, NM, USA. nmellios@salud.unm.edu.ORCID http://orcid.org/0000-0002-0310-1144
University of New Mexico · USHarvard University · USJohns Hopkins University · USKarolinska Institutet · SEStanley Medical Research Institute · US

Funding

Unfolded Protein Response and Autophagy in T Helper Cell Effector FunctionP20GM121176 · NIGMS · UNIVERSITY OF NEW MEXICO HEALTH SCIS CTR · PI Monica Rosas Lemus · 2017 to 2026
$24.9M
NIGMS NIH HHS P20 GM121176U.S. Department of Health & Human Services | NIH | National Institute of General Medical Sciences (NIGMS) P20GM121176
6 · The paper itself

Abstract

The ability of small secretory microvesicles known as exosomes to influence neuronal and glial function via their microRNA (miRNA) cargo has positioned them as a novel and effective method of cell-to-cell communication. However, little is known about the role of exosome-secreted miRNAs in the regulation of glutamate receptor gene expression and their relevance for schizophrenia (SCZ) and bipolar disorder (BD). Using mature miRNA profiling and quantitative real-time PCR (qRT-PCR) in the orbitofrontal cortex (OFC) of SCZ (N = 29; 20 male and 9 female), BD (N = 26; 12 male and 14 female), and unaffected control (N = 25; 21 male and 4 female) subjects, we uncovered that miR-223, an exosome-secreted miRNA that targets glutamate receptors, was increased at the mature miRNA level in the OFC of SCZ and BD patients with positive history of psychosis at the time of death and was inversely associated with deficits in the expression of its targets glutamate ionotropic receptor NMDA-type subunit 2B (GRIN2B) and glutamate ionotropic receptor AMPA-type subunit 2 (GRIA2). Furthermore, changes in miR-223 levels in the OFC were positively and negatively correlated with inflammatory and GABAergic gene expression, respectively. Moreover, miR-223 was found to be enriched in astrocytes and secreted via exosomes, and antipsychotics were shown to control its cellular and exosomal localization in a cell-specific manner. Furthermore, addition of astrocytic exosomes in neuronal cultures resulted in a significant increase in miR-223 expression and a notable reduction in Grin2b and Gria2 mRNA levels, which was strongly inversely associated with miR-223 expression. Lastly, inhibition of astrocytic miR-223 abrogated the exosomal-mediated reduction in neuronal Grin2b expression. Taken together, our results demonstrate that the exosomal secretion of a psychosis-altered and glial-enriched miRNA that controls neuronal gene expression is regulated by antipsychotics.

Indexed as

AnimalsAntipsychotic AgentsCells, CulturedExosomesFemaleGene ExpressionHumansMaleMiceMice, Inbred C57BLMicroRNAsRatsRats, Sprague-DawleyReceptors, N-Methyl-D-AspartateSchizophreniaAntipsychotic AgentsMicroRNAsMIR223, humanNR2B NMDA receptorReceptors, N-Methyl-D-Aspartate

Identifiers

PMID31775160
PMCPMC7021900
OpenAlexW2990923180

What OpenQuestion holds

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LicenceCC BY
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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.