Evidence map›Paper›PMID 22796551›Full record

ArticleBrain, behavior, and immunity2012

β-Adrenergic receptor mediated increases in activation and function of natural killer cells following repeated social disruption.

Andrew J Tarr, Nicole D Powell, Brenda F Reader, Neela S Bhave, Amanda L Roloson, William E Carson, John F Sheridan

Open access · greenAbstract read
In one paragraph

Article in Brain, behavior, and immunity, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 30 papers.

0numbers the graph read from it
0cells of the map it votes in
30citing papers in PubMed
1.5field-weighted citation impact, top 19% 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

30 citing papers in PubMed, 45 citations in OpenAlex.

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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

7 authors at 2 institutions in 1 country.

Andrew J TarrDivision of Oral Biology College of Dentistry, The Ohio State University, 305 W. 12th Ave. Columbus, OH 43210, USA. andrew.tarr@osumc.edu
Nicole D Powell
Brenda F Reader
Neela S Bhave
Amanda L Roloson
William E Carson
John F Sheridan
The Ohio State University · USInstitute for Behavioral Medicine · US

Funding

TWO SIGNAL REQUIREMENT FOR NATURAL KILLER IMMUNITYP01CA095426 · NCI · OHIO STATE UNIVERSITY · PI CALIGIURI, MICHAEL A · 2002 to 2016
$29.6M
Comprehensive Training in Oral &Craniofacial SciencesT32DE014320 · NIDCR · OHIO STATE UNIVERSITY · PI SHERIDAN, JOHN F · 2001 to 2022
$10.2M
STRESS-INDUCED IMMUNOSUPPRESSION OF ANTIVIRAL IMMUNITYR01MH046801 · NIMH · OHIO STATE UNIVERSITY · PI SHERIDAN, JOHN F · 1991 to 2008
$2.7M
Social threat primes myeloid progenitor cells and microglia: role in anxietyR01MH093473 · NIMH · OHIO STATE UNIVERSITY · PI SHERIDAN, JOHN F · 2012 to 2016
$1.9M
Microenvironmental changes on NK cell responses to primary HSV-1F32DE022230 · NIDCR · OHIO STATE UNIVERSITY · PI TARR, ANDREW J. · 2011 to 2011
$49k
NCI NIH HHS P01 CA095426NIDCR NIH HHS F32 DE-022230NIDCR NIH HHS F32 DE022230NIDCR NIH HHS T32 DE-014320NIDCR NIH HHS T32 DE014320NIMH NIH HHS R01 MH-046801NIMH NIH HHS R01 MH046801NIMH NIH HHS R01 MH093473
6 · The paper itself

Abstract

Natural killer (NK) cells are specialized innate lymphocytes important in the early defense against tumor and virus bearing cells. Many factors influence the immune system's effectiveness against pathogens, including stress. Social disruption (SDR) "primes" macrophages/monocytes and dendritic cells thereby enhancing their anti-microbial function. What remains unclear is whether similar responses are evident in NK cells. Current studies investigated the cellular distribution and activation/inhibitory phenotypes of NK cells in the spleen, lung, and blood of C57BL/6 male mice following SDR. Furthermore, cytolytic activity and anti-viral cytokine production of splenic NK cells were determined. Lastly, β-adrenergic receptor (β-AR) signaling was investigated to determine possible mechanisms behind the SDR-induced NK cell alterations. Results indicated NK cells from SDR mice have increased expression of CD16 and CD69 and reduced NKG2a and Ly49a expression on splenic CD3-/DX5+ NK cells indicative of an activated phenotype, both immediately and 14h post-SDR. Administration of propranolol (10mg/kg; non-selective β-adrenergic receptor antagonist) was shown to block these "priming" effects at the 14h time-point. In the lung, SDR had similar effects on activation and inhibitory receptors 14h post-SDR, however no alterations were evident in the blood besides increased NK cells directly after SDR. Additionally, splenic NK cells from SDR mice had increased CD107a surface expression, cytolytic activity, and IFN-γ production was increased upon costimulation with IgG and IL-2 ex vivo. Collectively, these data suggest that social stress "primes" NK cells in the spleen and lung to be more proficient in their cytolytic and anti-viral/tumor effecter functions through β-adrenergic receptor dependent signaling.

Indexed as

Social BehaviorAnimalsBehavior, AnimalDisease Models, AnimalKiller Cells, NaturalLungMaleMiceMice, Inbred C57BLReceptors, Adrenergic, betaSignal TransductionSpleenReceptors, Adrenergic, beta

Identifiers

PMID22796551
PMCPMC3468689
OpenAlexW2006652633

What OpenQuestion holds

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Read underepoch 390

Registered trials

None linked

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.