Evidence map›Paper›PMID 39229102›Full record

ArticlebioRxiv : the preprint server for biology2024

Acute systemic macrophage depletion in osteoarthritic mice alleviates pain-related behaviors and does not affect joint damage.

Terese Geraghty, Shingo Ishihara, Alia M Obeidat, Natalie S Adamczyk, Rahel S Hunter, Jun Li, Lai Wang, Hoomin Lee, Frank C Ko, Anne-Marie Malfait and 1 more

Abstract readPreprint
In one paragraph

Article in bioRxiv : the preprint server for biology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
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

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

11 authors.

Terese GeraghtyRush University Medical Center, Department of Internal Medicine, Division of Rheumatology, Chicago, IL USA.
Shingo IshiharaRush University Medical Center, Department of Internal Medicine, Division of Rheumatology, Chicago, IL USA.
Alia M ObeidatRush University Medical Center, Department of Internal Medicine, Division of Rheumatology, Chicago, IL USA.
Natalie S AdamczykRush University Medical Center, Department of Internal Medicine, Division of Rheumatology, Chicago, IL USA.
Rahel S HunterRush University Medical Center, Department of Internal Medicine, Division of Rheumatology, Chicago, IL USA.
Jun LiRush University Medical Center, Department of Internal Medicine, Division of Rheumatology, Chicago, IL USA.
Lai WangRush University Medical Center, Department of Internal Medicine, Division of Rheumatology, Chicago, IL USA.
Hoomin LeeRush University Medical Center, Department of Internal Medicine, Division of Rheumatology, Chicago, IL USA.
Frank C KoRush University Medical Center, Department of Internal Medicine, Division of Rheumatology, Chicago, IL USA.
Anne-Marie MalfaitRush University Medical Center, Department of Internal Medicine, Division of Rheumatology, Chicago, IL USA.
Rachel E MillerRush University Medical Center, Department of Internal Medicine, Division of Rheumatology, Chicago, IL USA.ORCID 0000-0002-4486-5757

Funding

Osteoarthritis Progression And Sensory Pathway AlterationsR01AR064251 · NIAMS · RUSH UNIVERSITY MEDICAL CENTER · PI MALFAIT, ANNE-MARIE, MILLER, RICHARD J · 2013 to 2025
$7.6M
Molecular Pathways of Pain Generation in OsteoarthritisR01AR060364 · NIAMS · RUSH UNIVERSITY MEDICAL CENTER · PI MALFAIT, ANNE-MARIE · 2011 to 2025
$6.0M
Neurobiology Core CP30AR079206 · NIAMS · RUSH UNIVERSITY MEDICAL CENTER · PI Anne-Marie Malfait · 2021 to 2026
$4.7M
The Role of Mechanosensation Pathways in Osteoarthritis Joint Damage and PainR01AR077019 · NIAMS · RUSH UNIVERSITY MEDICAL CENTER · PI Rachel Elizabeth Miller · 2021 to 2026
$2.7M
Pre and Post-Doctoral Training in Joint HealthT32AR073157 · NIAMS · RUSH UNIVERSITY MEDICAL CENTER · PI D Rick Sumner · 2019 to 2026
$2.3M
Piezo2-mediated neuroplasticity in osteoarthritisF31AR083277 · NIAMS · RUSH UNIVERSITY MEDICAL CENTER · PI ADAMCZYK, NATALIE · 2023 to 2024
$90k
Elucidating how macrophages contribute to osteoarthritis painF32AR081129 · NIAMS · RUSH UNIVERSITY MEDICAL CENTER · PI GERAGHTY, TERESE · 2022 to 2022
$72k
NIAMS NIH HHS F31 AR083277NIAMS NIH HHS F32 AR081129NIAMS NIH HHS P30 AR079206NIAMS NIH HHS R01 AR060364NIAMS NIH HHS R01 AR064251NIAMS NIH HHS R01 AR077019NIAMS NIH HHS T32 AR073157
6 · The paper itself

Abstract

Background: Osteoarthritis (OA) is a painful degenerative joint disease and a leading source of years lived with disability globally due to inadequate treatment options. Neuroimmune interactions reportedly contribute to OA pain pathogenesis. Notably, in rodents, macrophages in the DRG are associated with onset of persistent OA pain. Our objective was to determine the effects of acute systemic macrophage depletion on pain-related behaviors and joint damage using surgical mouse models in both sexes. Methods: We depleted CSF1R+ macrophages by treating male macrophage Fas-induced apoptosis (MaFIA) transgenic mice 8- or 16-weeks Results: Eight- and 16-weeks Conclusions: Acute systemic macrophage depletion reduced the levels of pro-inflammatory macrophages in the DRG and alleviated pain-related behaviors in established surgically induced OA in mice of both sexes, without affecting joint damage. Overall, these studies provide insight into immune cell regulation in the DRG during OA.

Indexed as

dorsal root gangliamacrophagesneuroimmuneOsteoarthritispainsensitization

Identifiers

PMID39229102
PMCPMC11370380

What Socratic holds

Textmetadata
LicenceCC BY-NC-ND
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 Socratic graph.