Evidence map›Paper›PMID 26281717›Full record

ArticleBiological psychiatry2016

Sympathetic Release of Splenic Monocytes Promotes Recurring Anxiety Following Repeated Social Defeat.

Daniel B McKim, Jenna M Patterson, Eric S Wohleb, Brant L Jarrett, Brenda F Reader, Jonathan P Godbout, John F Sheridan

Open access · greenAbstract read
In one paragraph

Article in Biological psychiatry, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 79 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
79citing papers in PubMed, 2 pooled it
4.0field-weighted citation impact, top 5% 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

79 citing papers in PubMed, 2 syntheses or guidelines pooled it, 137 citations in OpenAlex.

  1. Pooled it
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  13. Glycolytic metabolism: Food for immune cells, fuel for depression?Brain, behavior, & immunity - health · 2024
    Article
  14. Article
  15. Review
  16. Article
  17. Article
  18. Social stress induces autoimmune responses against the brain.Proceedings of the National Academy of Sciences of the United States of America · 2023
    Article
  19. Article
  20. Article

19 more citing papers are in PubMed but not listed here.

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

7 authors at 1 institution in 1 country.

Daniel B McKimDivision of Biosciences, College of Dentistry, The Ohio State University, Columbus, Ohio; Department of Neuroscience, College of Medicine, The Ohio State University, Columbus, Ohio.
Jenna M PattersonDivision of Biosciences, College of Dentistry, The Ohio State University, Columbus, Ohio; Department of Neuroscience, College of Medicine, The Ohio State University, Columbus, Ohio.
Eric S WohlebDivision of Biosciences, College of Dentistry, The Ohio State University, Columbus, Ohio; Department of Neuroscience, College of Medicine, The Ohio State University, Columbus, Ohio; Department of Psychiatry, School of Medicine, Yale University, New Haven, Connecticut.
Brant L JarrettDivision of Biosciences, College of Dentistry, The Ohio State University, Columbus, Ohio; Department of Neuroscience, College of Medicine, The Ohio State University, Columbus, Ohio.
Brenda F ReaderDivision of Biosciences, College of Dentistry, The Ohio State University, Columbus, Ohio.
Jonathan P GodboutInstitute for Behavioral Medicine Research, The Ohio State University, Columbus, Ohio; Center for Brain and Spinal Cord Repair, The Ohio State University, Columbus, Ohio.
John F SheridanDivision of Biosciences, College of Dentistry, The Ohio State University, Columbus, Ohio; Institute for Behavioral Medicine Research, The Ohio State University, Columbus, Ohio; Center for Brain and Spinal Cord Repair, The Ohio State University, Columbus, Ohio. Electronic address: sheridan.1@osu.edu.
The Ohio State University · US

Funding

Comprehensive Training in Oral &Craniofacial SciencesT32DE014320 · NIDCR · OHIO STATE UNIVERSITY · PI SHERIDAN, JOHN F · 2001 to 2022
$10.2M
Brain region dependent trafficking of myeloid precursor cells in repeated defeat.R01MH097243 · NIMH · OHIO STATE UNIVERSITY · PI SHERIDAN, JOHN F · 2013 to 2017
$2.2M
Social threat primes myeloid progenitor cells and microglia: role in anxietyR01MH093473 · NIMH · OHIO STATE UNIVERSITY · PI SHERIDAN, JOHN F · 2012 to 2016
$1.9M
Spleen Monocyte Progenitors Promote Recurring AnxietyF31MH109234 · NIMH · OHIO STATE UNIVERSITY · PI MCKIM, DANIEL BOYCE · 2015 to 2017
$46k
NIDCR NIH HHS T32 DE014320NIMH NIH HHS F31 MH109234NIMH NIH HHS R01 MH093473NIMH NIH HHS R01 MH097243
6 · The paper itself

Abstract

backgroundNeuroinflammatory signaling may contribute to the pathophysiology of chronic anxiety disorders. Previous work showed that repeated social defeat (RSD) in mice promoted stress-sensitization that was characterized by the recurrence of anxiety following subthreshold stress 24 days after RSD. Furthermore, splenectomy following RSD prevented the recurrence of anxiety in stress-sensitized mice. We hypothesize that the spleen of RSD-exposed mice became a reservoir of primed monocytes that were released following neuroendocrine activation by subthreshold stress.

methodsMice were subjected to subthreshold stress (i.e., single cycle of social defeat) 24 days after RSD, and immune and behavioral measures were taken.

resultsSubthreshold stress 24 days after RSD re-established anxiety-like behavior that was associated with egress of Ly6C(hi) monocytes from the spleen. Moreover, splenectomy before RSD blocked monocyte trafficking to the brain and prevented anxiety-like behavior following subthreshold stress. Splenectomy, however, had no effect on monocyte accumulation or anxiety when determined 14 hours after RSD. In addition, splenocytes cultured 24 days after RSD exhibited a primed inflammatory phenotype. Peripheral sympathetic inhibition before subthreshold stress blocked monocyte trafficking from the spleen to the brain and prevented the re-establishment of anxiety in RSD-sensitized mice. Last, β-adrenergic antagonism also prevented splenic monocyte egress after acute stress.

conclusionsThe spleen served as a unique reservoir of primed monocytes that were readily released following sympathetic activation by subthreshold stress that promoted the re-establishment of anxiety. Collectively, the long-term storage of primed monocytes in the spleen may have a profound influence on recurring anxiety disorders.

Indexed as

AnimalsAnxietyBrainCell MovementCohort StudiesDisease Models, AnimalDominance-SubordinationGuanethidineMaleMice, Inbred C57BLMonocytesNeuroimmunomodulationSpleenSplenectomyStress, PsychologicalSympathetic Nervous SystemGuanethidineSympatholyticsAnxietyMacrophagesMicrogliaNeuroinflammationPTSDStress

Identifiers

PMID26281717
PMCPMC4728074
OpenAlexW1600219138

What OpenQuestion holds

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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.