Evidence map›Paper›PMID 34718176›Full record

ArticleThe spine journal : official journal of the North American Spine Society2022

Heterogeneous macrophages contribute to the pathology of disc herniation induced radiculopathy.

Li Jin, Li Xiao, Mengmeng Ding, Aixing Pan, Gary Balian, Sun-Sang J Sung, Xudong Joshua Li

Open access · greenAbstract read
In one paragraph

Article in The spine journal : official journal of the North American Spine Society, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
2.4field-weighted citation impact, top 11% 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

14 citing papers in PubMed, 20 citations in OpenAlex.

  1. Flow Cytometry Study of Immune Cell Subpopulations from the Mouse Vertebral Bone Marrow and Intervertebral Disc Following Endplate Microfracture.Biocell : official journal of the Sociedades Latinoamericanas de Microscopia Electronica ... et. al · 2026
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  14. Frontiers in pain research (Lausanne, Switzerland) · 2022
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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

7 authors at 2 institutions in 2 countries.

Li JinDepartment of Orthopaedic Surgery, University of Virginia, Charlottesville, VA 22908, USA.
Li XiaoDepartment of Orthopaedic Surgery, University of Virginia, Charlottesville, VA 22908, USA.
Mengmeng DingDepartment of Orthopaedic Surgery, University of Virginia, Charlottesville, VA 22908, USA; Department of Anesthesiology, Shengjing hospital, China Medical University, Shenyang, China.
Aixing PanDepartment of Orthopaedic Surgery, University of Virginia, Charlottesville, VA 22908, USA; Department of Orthopaedic Surgery, Chaoyang Hospital, Capital Medical School, Beijing, China.
Gary BalianDepartment of Orthopaedic Surgery, University of Virginia, Charlottesville, VA 22908, USA; Department of Biochemistry and Molecular Genetics, University of Virginia, Charlottesville, VA 22908, USA.
Sun-Sang J SungDepartment of Medicine and Center for Immunity, Inflammation, and Regenerative Medicine, University of Virginia, Charlottesville, VA 22908, USA.
Xudong Joshua LiDepartment of Orthopaedic Surgery, University of Virginia, Charlottesville, VA 22908, USA; Department of Biomedical Engineering, University of Virginia, Charlottesville, VA 22904, USA. Electronic address: xl2n@virginia.edu.
University of Virginia · USUniversity of Virginia Medical Center · US

Funding

Deciphering Macrophage Phenotype and Function in Disc Herniation and associated Back/leg PainR01AR078888 · NIAMS · UNIVERSITY OF VIRGINIA · PI XUDONG J. LI · 2022 to 2026
$1.8M
Systemic Application for Injury Site Specific Delivery via Neutrophils to Treat BR01AR064792 · NIAMS · UNIVERSITY OF VIRGINIA · PI LI, XUDONG J. · 2013 to 2018
$1.3M
Disc-on-a-chip: microfluidic nutrition and biomechanical loading integrated mouse disc culture systemR21AR072334 · NIAMS · UNIVERSITY OF VIRGINIA · PI LI, XUDONG J. · 2018 to 2019
$391k
An ex vivo system to model the inflammatory microenvironment of human disc herniationR21AR078547 · NIAMS · UNIVERSITY OF VIRGINIA · PI LI, XUDONG J., POMPANO, REBECCA R · 2021 to 2021
$388k
NIAMS NIH HHS R01 AR064792NIAMS NIH HHS R01 AR078888NIAMS NIH HHS R21 AR072334NIAMS NIH HHS R21 AR078547
6 · The paper itself

Abstract

background contextMacrophages play important roles in the progression of intervertebral disc herniation and radiculopathy. PURPOSE: To better understand the roles of macrophages in this process, we developed a new mouse model that mimics human radiculopathy. STUDY DESIGN/

settingA preclinical randomized animal study.

methodsThree types of surgeries were performed in randomly assigned Balb/c mice. These were spinal nerve exposure, traditional anterior disc puncture, and lateral disc puncture with nerve exposure (n=16/group). For the nerve exposure group, the left L5 spinal nerve was exposed without disc injury. For the traditional anterior puncture, L5/6 disc was punctured by an anterior approach as previously established. For lateral puncture with nerve exposure, the left L5 spinal nerve was exposed by removing the psoas major muscle fibers, and the L5/6 disc was punctured laterally on the left side with a 30G needle, allowing the nucleus to protrude toward the L5 spinal nerve. Mechanical hyperalgesia (pain sensitivity) of hind paws was assessed with electronic von Frey assay on alternative day for up to 2 weeks. MRI, histology, and immunostaining were performed to confirm disc herniation and inflammation.

resultsIpsilateral pain in the lateral puncture with nerve exposure group was significantly greater than the other groups. Pro-inflammatory cytokines IL-1β and IL-6 were markedly elevated at the hernia sites of both puncture groups and the spinal nerve of lateral puncture with never exposure group on postoperative day 7. Heterogeneous populations of macrophages were detected in the infiltration tissue of this mouse model and in tissue from patients undergone discectomy.

conclusionsWe have established a new mouse model that mimics human radiculopathy and demonstrated that a mixed phenotype of macrophages contribute to the pathogenesis of acute discogenic radiculopathy. CLINICAL SIGNIFICANCE: This study provides a clinically relevant in vivo animal model to elucidate complex interactions of disc herniation and radicular pain, which may present opportunities for the development of macrophage-anchored therapeutics to manage radiculopathy.

Indexed as

Intervertebral DiscIntervertebral Disc DisplacementRadiculopathyAnimalsLumbar VertebraeMacrophagesMiceMice, Inbred BALB CAnimal modelDisc DegenerationDisc herniationInflammationLow back painMacrophagesRadiculopathy

Identifiers

PMID34718176
PMCPMC8957503
OpenAlexW3209991565

What OpenQuestion holds

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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.