Evidence map›Paper›PMID 37309034›Full record

ArticleJournal of leukocyte biology2023

Aging modulates homeostatic leukocyte trafficking to the peritoneal cavity in a sex-specific manner.

Sophie J Hopkin, Laleh Pezhman, Jenefa Begum, Dean Kavanagh, Helen M McGettrick, Asif J Iqbal, Myriam Chimen

Open access · hybridAbstract read
In one paragraph

Article in Journal of leukocyte biology, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
1.5field-weighted citation impact, top 17% 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

5 citing papers in PubMed, 9 citations in OpenAlex.

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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

7 authors at 1 institution in 1 country.

Sophie J HopkinInstitute of Cardiovascular Sciences, University of Birmingham, Birmingham, B15 2TT, United Kingdom.
Laleh PezhmanInstitute of Inflammation and Ageing, University of Birmingham, Birmingham, B15 2TT, United Kingdom.
Jenefa BegumInstitute of Cardiovascular Sciences, University of Birmingham, Birmingham, B15 2TT, United Kingdom.
Dean KavanaghInstitute of Cardiovascular Sciences, University of Birmingham, Birmingham, B15 2TT, United Kingdom.
Helen M McGettrickInstitute of Inflammation and Ageing, University of Birmingham, Birmingham, B15 2TT, United Kingdom.
Asif J IqbalInstitute of Cardiovascular Sciences, University of Birmingham, Birmingham, B15 2TT, United Kingdom.ORCID 0000-0002-3224-3651
Myriam ChimenInstitute of Inflammation and Ageing, University of Birmingham, Birmingham, B15 2TT, United Kingdom.ORCID 0000-0002-5950-8840
University of Birmingham · GB

Funding

British Heart Foundation FS/20/2/34799Medical Research Council MR/P021220/1Medical Research Council MR/T028025/1Versus Arthritis
6 · The paper itself

Abstract

Aging is associated with exacerbated systemic inflammation (inflammaging) and the progressive loss of immune system function (immunosenescence). Leukocyte migration is necessary for effective immunity; however, dysregulated trafficking of leukocytes into tissue contributes to inflammaging and the development of age-related inflammatory diseases. Aging modulates leukocyte trafficking under inflammatory conditions; however, whether aging modulates leukocyte trafficking under homeostatic conditions remains to be elucidated. Although immune responses are evidently sexually dimorphic, limited studies have investigated the effect of sex on age-related changes to leukocyte trafficking processes. Here, we investigated age-related and sex-specific changes to the leukocyte populations within the peritoneal cavity of young (3-mo), middle-aged (18-mo) and old (21-mo) male and female wild-type mice in the steady state. We found an age-related increase in the number of leukocytes within the peritoneal cavity of female mice, predominantly B cells, which may reflect increased trafficking through this tissue with age. This was accompanied by an increased inflammatory environment within the aged cavity, including increased levels of chemoattractants, including B cell chemoattractants CXCL13 and CCL21, soluble adhesion molecules, and proinflammatory cytokines, which was more pronounced in aged female mice. Intravital microscopy techniques revealed altered vascular structure and increased vascular permeability within the peritoneal membrane of aged female mice, which may support increased leukocyte trafficking to the cavity with age. Together, these data indicate that aging affects homeostatic leukocyte trafficking processes in a sex-specific fashion.

Indexed as

LeukocytesPeritoneal CavityAnimalsChemotactic FactorsFemaleInflammationMaleMicePeritoneumChemotactic Factorsaginginflammationleukocyte traffickingsexual dimorphismT cells

Identifiers

PMID37309034
PMCPMC10533226
OpenAlexW4380422120

What OpenQuestion holds

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LicenceCC BY
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.