Evidence map›Paper›PMID 38274272›Full record

ArticleFrontiers in cell and developmental biology2023

Identification of a novel, MSC-induced macrophage subtype via single-cell sequencing: implications for intervertebral disc degeneration therapy.

Jinsha Koroth, Casey Chitwood, Ramya Kumar, Wei-Han Lin, Benjamin T Reves, Todd Boyce, Theresa M Reineke, Arin M Ellingson, Casey P Johnson, Laura S Stone and 4 more

Open access · goldAbstract read
In one paragraph

Article in Frontiers in cell and developmental biology, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed, 1 pooled it
1.8field-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

4 citing papers in PubMed, 1 synthesis or guideline pooled it, 4 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Article
  4. Review
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

14 authors at 5 institutions in 1 country.

Jinsha KorothDepartment of Orthopedic Surgery, Medical School, University of Minnesota, Minneapolis, MN, United States.
Casey ChitwoodDepartment of Biomedical Engineering, College of Science and Engineering, University of Minnesota, Minneapolis, MN, United States.
Ramya KumarDepartment of Chemical and Biological Engineering, Colorado School of Mines, Golden, CO, United States.
Wei-Han LinDepartment of Biomedical Engineering, College of Science and Engineering, University of Minnesota, Minneapolis, MN, United States.
Benjamin T RevesMedtronic, Memphis, TN, United States.
Todd BoyceMedtronic, Memphis, TN, United States.
Theresa M ReinekeDepartment of Chemistry, College of Science and Engineering, University of Minnesota, Minneapolis, MN, United States.
Arin M EllingsonDepartment of Orthopedic Surgery, Medical School, University of Minnesota, Minneapolis, MN, United States.
Casey P JohnsonDepartment of Veterinary Clinical Sciences, College of Veterinary Medicine, University of Minnesota, St. Paul, MN, United States.
Laura S StoneDepartment of Anesthesiology, School of Medicine, University of Minnesota, Minneapolis, MN, United States.
Kimberly C ChaffinMedtronic, Minneapolis, MN, United States.
Narendra K SimhaMedtronic, Minneapolis, MN, United States.
Brenda M OgleDepartment of Chemical and Biological Engineering, Colorado School of Mines, Golden, CO, United States.
Elizabeth W BradleyDepartment of Orthopedic Surgery, Medical School, University of Minnesota, Minneapolis, MN, United States.
University of Minnesota · USMedtronic (United States) · USColorado School of Mines · USUniversity of Minnesota Medical Center · USResonance Research (United States) · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Intervertebral disc (IVD) degeneration is a common pathological condition associated with low back pain. Recent evidence suggests that mesenchymal signaling cells (MSCs) promote IVD regeneration, but underlying mechanisms remain poorly defined. One postulated mechanism is via modulation of macrophage phenotypes. In this manuscript, we tested the hypothesis that MSCs produce trophic factors that alter macrophage subsets. To this end, we collected conditioned medium from human, bone marrow-derived STRO3

Indexed as

back painCCL2CoffilinIFN gammasingle cell sequence (scRNA-seq)STRO3

Identifiers

PMID38274272
PMCPMC10808728
OpenAlexW4390745014

What OpenQuestion holds

Textmetadata
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.