Evidence map›Paper›PMID 35641477›Full record

ArticleBone research2022

Neuron-to-vessel signaling is a required feature of aberrant stem cell commitment after soft tissue trauma.

Qizhi Qin, Mario Gomez-Salazar, Masnsen Cherief, Chase A Pagani, Seungyong Lee, Charles Hwang, Robert J Tower, Sharon Onggo, Yuxiao Sun, Abhinav Piplani and 5 more

Open access · goldAbstract read
In one paragraph

Article in Bone research, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 24 papers.

0numbers the graph read from it
0cells of the map it votes in
24citing papers in PubMed
5.4field-weighted citation impact, top 3% 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

24 citing papers in PubMed, 35 citations in OpenAlex.

  1. Clec3bBone research · 2026
    Article
  2. Review
  3. Article
  4. Single-cell sequencing uncovers sensory neuron-mediated CGRP signaling as a driver of sarcoma progression.Proceedings of the National Academy of Sciences of the United States of America · 2025
    Article
  5. Review
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  20. Tppp3Bone research · 2023
    Article
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

15 authors at 4 institutions in 1 country.

Qizhi Qin *Department of Pathology, Johns Hopkins University, Baltimore, MD, 21205, USA.
Mario Gomez-Salazar *Department of Pathology, Johns Hopkins University, Baltimore, MD, 21205, USA.
Masnsen CheriefDepartment of Pathology, Johns Hopkins University, Baltimore, MD, 21205, USA.
Chase A PaganiCenter for Organogenesis and Trauma, Department of Surgery, University of Texas, Southwestern, TX, USA.
Seungyong LeeDepartment of Pathology, Johns Hopkins University, Baltimore, MD, 21205, USA.
Charles HwangDepartment of Plastic Surgery, Harvard, Cambridge, MA, 02138, USA.
Robert J TowerCenter for Organogenesis and Trauma, Department of Surgery, University of Texas, Southwestern, TX, USA.ORCID http://orcid.org/0000-0001-5856-5758
Sharon OnggoDepartment of Pathology, Johns Hopkins University, Baltimore, MD, 21205, USA.
Yuxiao SunCenter for Organogenesis and Trauma, Department of Surgery, University of Texas, Southwestern, TX, USA.
Abhinav PiplaniDepartment of Pathology, Johns Hopkins University, Baltimore, MD, 21205, USA.
Zhao LiDepartment of Pathology, Johns Hopkins University, Baltimore, MD, 21205, USA.
Sowmya RameshDepartment of Pathology, Johns Hopkins University, Baltimore, MD, 21205, USA.
Thomas L ClemensDepartment of Orthopaedics, Johns Hopkins University, Baltimore, MD, 21205, USA.
Benjamin LeviCenter for Organogenesis and Trauma, Department of Surgery, University of Texas, Southwestern, TX, USA. Benjamin.Levi@utsouthwestern.edu.
Aaron W JamesDepartment of Pathology, Johns Hopkins University, Baltimore, MD, 21205, USA. awjames@jhmi.edu.ORCID http://orcid.org/0000-0002-2002-622X
Johns Hopkins University · USOrganogenesis (United States) · USSouthwestern Medical Center · USUnited States Department of Veterans Affairs · US

Funding

Impact of peripheral nerves on mesenchymal cell fate in extremity traumaR01AR079171 · NIAMS · UT SOUTHWESTERN MEDICAL CENTER · PI JAMES, AARON W, LEVI, BENJAMIN · 2021 to 2024
$3.0M
Neuronal Regulation of Skeletal Development and RepairR01AR068934 · NIAMS · JOHNS HOPKINS UNIVERSITY · PI CLEMENS, THOMAS L · 2015 to 2019
$1.8M
Targeting Molecular and Cellular Mediators of Inflammation to Prevent Pathologic Cell Differentiation and Heterotopic OssificationR01AR071379 · NIAMS · UT SOUTHWESTERN MEDICAL CENTER · PI LEVI, BENJAMIN · 2017 to 2021
$1.5M
Direct and indirect contributions of perivascular stem cells to bone healingR01AR070773 · NIAMS · JOHNS HOPKINS UNIVERSITY · PI JAMES, AARON W · 2017 to 2021
$1.4M
Role of sensory nerves in cranial bone repairR21DE027922 · NIDCR · JOHNS HOPKINS UNIVERSITY · PI CLEMENS, THOMAS L, JAMES, AARON W · 2018 to 2019
$450k
NIAMS NIH HHS R01 AR068934NIAMS NIH HHS R01 AR070773NIAMS NIH HHS R01 AR071379NIAMS NIH HHS R01 AR079171NIDCR NIH HHS R21 DE027922
6 · The paper itself

Abstract

The functional interdependence of nerves and blood vessels is a well-established concept during tissue morphogenesis, yet the role of neurovascular coupling in proper and aberrant tissue repair is an emerging field of interest. Here, we sought to define the regulatory relationship of peripheral nerves on vasculature in a severe extremity trauma model in mice, which results in aberrant cell fate and heterotopic ossification (HO). First, a high spatial degree of neurovascular congruency was observed to exist within extremity injury associated heterotopic ossification. Vascular and perivascular cells demonstrate characteristic responses to injury, as assessed by single cell RNA sequencing. This vascular response to injury was blunted in neurectomized mice, including a decrease in endothelial proliferation and type H vessel formation, and a downregulation of key transcriptional networks associated with angiogenesis. Independent mechanisms to chemically or genetically inhibit axonal ingrowth led to similar deficits in HO site angiogenesis, a reduction in type H vessels, and heterotopic bone formation. Finally, a combination of single cell transcriptomic approaches within the dorsal root ganglia identified key neural-derived angiogenic paracrine factors that may mediate neuron-to-vascular signaling in HO. These data provide further understanding of nerve-to-vessel crosstalk in traumatized soft tissues, which may reflect a key determinant of mesenchymal progenitor cell fate after injury.

Identifiers

PMID35641477
PMCPMC9156761
OpenAlexW4281982957

What OpenQuestion holds

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Registered trials

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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.