Evidence map›Paper›PMID 36625730›Full record

ArticleArthritis & rheumatology (Hoboken, N.J.)2023

Targeting Synovial Lymphatic Function as a Novel Therapeutic Intervention for Age-Related Osteoarthritis in Mice.

Xi Lin, Richard D Bell, Sarah E Catheline, Takahiro Takano, Andrew McDavid, Jennifer H Jonason, Edward M Schwarz, Lianping Xing

Open access · bronzeAbstract read
In one paragraph

Article in Arthritis & rheumatology (Hoboken, N.J.), 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers.

0numbers the graph read from it
0cells of the map it votes in
21citing papers in PubMed
5.5field-weighted citation impact, top 4% 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

21 citing papers in PubMed, 24 citations in OpenAlex.

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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

8 authors at 1 institution in 1 country.

Xi LinDepartment of Pathology and Laboratory Medicine, University of Rochester Medical Center, Rochester, New York.ORCID 0000-0001-5905-5311
Richard D BellCenter for Musculoskeletal Research, University of Rochester Medical Center, Rochester, New York.ORCID 0000-0003-1562-3879
Sarah E CathelineCenter for Musculoskeletal Research, University of Rochester Medical Center, Rochester, New York.
Takahiro TakanoDepartment of Pharmacology and Physiology, University of Rochester Medical Center, Rochester, New York.
Andrew McDavidDepartment of Biostatistics and Computational Biology, University of Rochester Medical Center, Rochester, New York.
Jennifer H JonasonCenter for Musculoskeletal Research, University of Rochester Medical Center, Rochester, New York.ORCID 0000-0002-2575-3979
Edward M SchwarzCenter for Musculoskeletal Research, University of Rochester Medical Center, Rochester, New York.
Lianping XingDepartment of Pathology and Laboratory Medicine, and Center for Musculoskeletal Research, University of Rochester Medical Center, Rochester, New York.
University of Rochester Medical Center · US

Funding

Rochester Resource-Based Center for Bone, Muscle and Orthopaedic Research (ROCSTARR) (Overall Application)P30AR069655 · NIAMS · UNIVERSITY OF ROCHESTER · PI Edward M. Schwarz · 2016 to 2026
$7.8M
Synovial lymphatics and osteoarthritis in agingR01AG059775 · NIA · UNIVERSITY OF ROCHESTER · PI XING, LIANPING · 2020 to 2024
$1.9M
Chondrocyte DNA Double-Strand Breaks in the Pathogenesis of OsteoarthritisR01AR076623 · NIAMS · UNIVERSITY OF ROCHESTER · PI JONASON, JENNIFER HARRELL · 2020 to 2024
$1.7M
Analgesic actions of adenosine A1 receptor along axonal tracts in chronic painR01AT007945 · NCCIH · UNIVERSITY OF ROCHESTER · PI TAKANO, TAKAHIRO · 2013 to 2017
$1.4M
Protein modification in bone cell regulationR21AR069789 · NIAMS · UNIVERSITY OF ROCHESTER · PI BOECKMAN, ROBERT K, XING, LIANPING · 2016 to 2017
$372k
NCCIH NIH HHS R01 AT007945NIAMS NIH HHS P30 AR069655NIAMS NIH HHS R01 AR076623NIAMS NIH HHS R21 AR069789NIA NIH HHS R01 AG059775
6 · The paper itself

Abstract

objectiveThe synovial lymphatic system (SLS) removes catabolic factors from the joint. Vascular endothelial growth factor C (VEGF-C) and its receptor, VEGFR-3, are crucial for lymphangiogenesis. However, their involvement in age-related osteoarthritis (OA) is unknown. This study was undertaken to determine whether the SLS and the VEGF-C/VEGFR-3 pathway contribute to the development and progression of age-related OA, using a murine model of naturally occurring joint disease.

methodsSLS function was assessed in the knees of young (3-month-old) and aged (19-24-month-old) male and female C57BL/6J mice via a newly established in vivo IVIS-dextran imaging approach, which, in addition to histology, was used to assess the effects of VEGF-C treatment on SLS function and OA pathology in aged mice. RNA-sequencing of synovial tissue was performed to explore molecular mechanisms of the disease in the mouse knee joints.

resultsResults showed that aged mice had impaired SLS function, including decreases in joint clearance (mean T

conclusionSLS function is reduced in the knee joints of aged mice due to decreased VEGF-C/VEGFR-3 signaling. VEGF-C treatment attenuates OA joint damage and improves synovial lymphatic drainage in aged mice. The SLS and VEGF-C/VEGFR-3 signaling represent novel physiopathologic mechanisms that could potentially be used as therapeutic targets for age-related OA.

Indexed as

OsteoarthritisVascular Endothelial Growth Factor CAnimalsFemaleMaleMiceMice, Inbred C57BLRNASynovial MembraneVascular Endothelial Growth Factor Receptor-3RNAVascular Endothelial Growth Factor CVascular Endothelial Growth Factor Receptor-3

Identifiers

PMID36625730
PMCPMC10238595
OpenAlexW4313986281

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.