Evidence map›Paper›PMID 22562814›Full record

ArticleJournal of molecular neuroscience : MN2012

Neuroglial expression of the MHCI pathway and PirB receptor is upregulated in the hippocampus with advanced aging.

Heather D VanGuilder Starkey, Colleen A Van Kirk, Georgina V Bixler, Caesar G Imperio, Vijay P Kale, Jacob M Serfass, Julie A Farley, Han Yan, Junie P Warrington, Song Han and 3 more

Abstract read
In one paragraph

Article in Journal of molecular neuroscience : MN, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 48 papers.

0numbers the graph read from it
0cells of the map it votes in
48citing papers in PubMed
2.4field-weighted citation impact, top 13% 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, 67 citations in OpenAlex.

  1. Article
  2. Review
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  10. Immune receptors and aging brain.Bioscience reports · 2024
    Review
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  13. Article
  14. Plasma βAlzheimer's research & therapy · 2023
    Article
  15. Article
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  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

13 authors at 2 institutions in 1 country.

Heather D VanGuilder StarkeyDepartment of Pharmacology, Penn State College of Medicine, Hershey, PA 17033, USA.
Colleen A Van Kirk
Georgina V Bixler
Caesar G Imperio
Vijay P Kale
Jacob M Serfass
Julie A Farley
Han Yan
Junie P Warrington
Song Han
Matthew Mitschelen
William E Sonntag
Willard M Freeman
Pennsylvania State University · USUniversity of Oklahoma Health Sciences Center · US

Funding

STRUCTURAL AND MOLECULAR CHANGES WITH AGEP01AG011370 · NIA · WAKE FOREST UNIVERSITY HEALTH SCIENCES · PI SONNTAG, WILLIAM EDMUND · 1995 to 2010
$10.7M
Cognitive Decline & Protein Expression Profiles in AgingR01AG026607 · NIA · UNIVERSITY OF OKLAHOMA HLTH SCIENCES CTR · PI SONNTAG, WILLIAM EDMUND · 2007 to 2011
$1.8M
Differentially expressed hippocampal miRNAs with age and cognitive declineF31AG038285 · NIA · PENNSYLVANIA STATE UNIV HERSHEY MED CTR · PI MANGOLD, COLLEEN A. · 2011 to 2013
$59k
NIA NIH HHS 1F31AG038285NIA NIH HHS 5R01AG026607NIA NIH HHS F31 AG038285NIA NIH HHS P01 AG011370NIA NIH HHS R01 AG026607
6 · The paper itself

Abstract

The hippocampus undergoes changes with aging that impact neuronal function, such as synapse loss and altered neurotransmitter release. Nearly half of the aged population also develops deficits in spatial learning and memory. To identify age-related hippocampal changes that may contribute to cognitive decline, transcriptomic analysis of synaptosome preparations from adult (12 months) and aged (28 months) Fischer 344-Brown Norway rats assessed for spatial learning and memory was performed. Bioinformatic analysis identified the MHCI pathway as significantly upregulated with aging. Age-related increases in mRNAs encoding the MHCI genes RT1-A1, RT1-A2, and RT1-A3 were confirmed by qPCR in synaptosomes and in CA1 and CA3 dissections. Elevated levels of the MHCI cofactor (B2m), antigen-loading components (Tap1, Tap2, Tapbp), and two known MHCI receptors (PirB, Klra2) were also confirmed. Protein expression of MHCI was elevated with aging in synaptosomes, CA1, and DG, while PirB protein expression was induced in both CA1 and DG. MHCI expression was localized to microglia and neuronal excitatory postsynaptic densities, and PirB was localized to neuronal somata, axons, and dendrites. Induction of the MHCI antigen processing and presentation pathway in hippocampal neurons and glia may contribute to age-related hippocampal dysfunction by increasing neuroimmune signaling or altering synaptic homeostasis.

Indexed as

Age FactorsAgingAnimalsCA1 Region, HippocampalChimeraDentate GyrusHistocompatibility AntigensHistocompatibility Antigens Class IMaleMaze LearningMemory DisordersMicrogliaNeuronsRatsRats, Inbred BNRats, Inbred F344Histocompatibility AntigensHistocompatibility Antigens Class Ihistocompatibility antigens RT, ratPirb protein, ratReceptors, Immunologic

Identifiers

PMID22562814
PMCPMC3414657
OpenAlexW1964055979

What OpenQuestion holds

Textmetadata
LicenceTDM
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.