Evidence map›Paper›PMID 36845161›Full record

ArticleFrontiers in immunology2023

BMP-6 promotes type 2 immune response during enhancement of rat mandibular bone defect healing.

Logan F McColl, Xizhao Chen, Michael D Solga, Kailo Schlegel, Sean P Haughey, Peter I Lobo, Kristen Fread, Eli Zunder, Ryan Cha, Stephen Park and 3 more

Open access · goldAbstract read
In one paragraph

Article in Frontiers in immunology, 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
1.7field-weighted citation impact, top 15% 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, 6 citations in OpenAlex.

  1. Article
  2. Article
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  4. Review
  5. 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

13 authors at 2 institutions in 1 country.

Logan F McCollDepartment of Orthopedic Surgery, University of Virginia Health System, Charlottesville, VA, United States.
Xizhao ChenDepartment of Orthopedic Surgery, University of Virginia Health System, Charlottesville, VA, United States.
Michael D SolgaFlow Cytometry Core Facility, University of Virginia, Charlottesville, VA, United States.
Kailo SchlegelDepartment of Nephrology, University of Virginia Health System, Charlottesville, VA, United States.
Sean P HaugheyDepartment of Orthopedic Surgery, University of Virginia Health System, Charlottesville, VA, United States.
Peter I LoboDepartment of Nephrology, University of Virginia Health System, Charlottesville, VA, United States.
Kristen FreadDepartment of Biomedical Engineering, University of Virginia, Charlottesville, VA, United States.
Eli ZunderDepartment of Biomedical Engineering, University of Virginia, Charlottesville, VA, United States.
Ryan ChaDepartment of Orthopedic Surgery, University of Virginia Health System, Charlottesville, VA, United States.
Stephen ParkDepartment of Otolaryngology-Head and Neck Surgery, University of Virginia Health System, Charlottesville, VA, United States.
J Jared ChristophelDepartment of Otolaryngology-Head and Neck Surgery, University of Virginia Health System, Charlottesville, VA, United States.
Quanjun CuiDepartment of Orthopedic Surgery, University of Virginia Health System, Charlottesville, VA, United States.
Abhijit S DigheDepartment of Orthopedic Surgery, University of Virginia Health System, Charlottesville, VA, United States.
University of Virginia Health System · USUniversity of Virginia · US

Funding

Inhibition of MSC1 stem cells and T cells to endorse bone healingR21AR072295 · NIAMS · UNIVERSITY OF VIRGINIA · PI CUI, QUANJUN · 2017 to 2018
$390k
NIAMS NIH HHS R21 AR072295
6 · The paper itself

Abstract

Introduction: Bone morphogenetic proteins (BMPs) are used as key therapeutic agents for the treatment of difficult fractures. While their effects on osteoprogenitors are known, little is known about their effects on the immune system. Methods: We used permutations of BMP-6 (B), vascular endothelial growth factor (V), and Hedgehog signaling pathway activator smoothened agonist (S), to treat a rat mandibular defect and investigated healing outcomes at week 8, in correlation with the cellular landscape of the immune cells in the fracture callus at week 2. Results: Maximum recruitment of immune cells to the fracture callus is known to occur at week 2. While the control, S, V, and VS groups remained as nonunions at week 8; all BMP-6 containing groups - B, BV, BS and BVS, showed near-complete to complete healing. This healing pattern was strongly associated with significantly higher ratios of CD4 T (CD45 Discussion: This study uncovers previously unidentified regulatory functions of BMP-6 and shows that BMP-6 enhances fracture healing by not only acting on osteoprogenitor stem cells but also by promoting type 2 immune response.

Indexed as

Bone Morphogenetic Protein 6Fractures, BoneAnimalsFracture HealingHedgehog ProteinsImmunityInterleukin-4RatsVascular Endothelial Growth Factor ABmp6 protein, ratBone Morphogenetic Protein 6Hedgehog ProteinsInterleukin-4Vascular Endothelial Growth Factor ABMPfracture healingmacrophagesstem cellsT cellstype 2 immune response

Identifiers

PMID36845161
PMCPMC9950738
OpenAlexW4319985420

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.