Evidence map›Paper›PMID 38472175›Full record

ArticleBone research2024

The HIF-1α/PLOD2 axis integrates extracellular matrix organization and cell metabolism leading to aberrant musculoskeletal repair.

Heeseog Kang, Amy L Strong, Yuxiao Sun, Lei Guo, Conan Juan, Alec C Bancroft, Ji Hae Choi, Chase A Pagani, Aysel A Fernandes, Michael Woodard and 8 more

Open access · goldAbstract read
In one paragraph

Article in Bone research, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 33 papers.

0numbers the graph read from it
0cells of the map it votes in
33citing papers in PubMed
12.7field-weighted citation impact, top 1% 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

33 citing papers in PubMed, 27 citations in OpenAlex.

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  5. Integrative Transcriptomic Profiling Delineates LTBP4-Driven Fibroblast Reprogramming Across the Ossification Continuum of the Ligamentum Flavum.FASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2026
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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

18 authors at 7 institutions in 1 country.

Heeseog KangCenter for Organogenesis, Regeneration and Trauma, Department of Surgery, University of Texas Southwestern, Dallas, TX, 75390, USA.ORCID http://orcid.org/0000-0002-2612-8585
Amy L StrongSection of Plastic Surgery, Department of Surgery, University of Michigan, Ann Arbor, MI, 48109, USA.
Yuxiao SunCenter for Organogenesis, Regeneration and Trauma, Department of Surgery, University of Texas Southwestern, Dallas, TX, 75390, USA.
Lei GuoQuantitative Biomedical Research Center, Peter O'Donnell Jr. School of Public Health, University of Texas Southwestern, Dallas, TX, 75390, USA.
Conan JuanCenter for Organogenesis, Regeneration and Trauma, Department of Surgery, University of Texas Southwestern, Dallas, TX, 75390, USA.ORCID http://orcid.org/0000-0002-0202-4298
Alec C BancroftCenter for Organogenesis, Regeneration and Trauma, Department of Surgery, University of Texas Southwestern, Dallas, TX, 75390, USA.ORCID http://orcid.org/0000-0001-9505-4762
Ji Hae ChoiCenter for Organogenesis, Regeneration and Trauma, Department of Surgery, University of Texas Southwestern, Dallas, TX, 75390, USA.ORCID http://orcid.org/0009-0001-1408-3383
Chase A PaganiCenter for Organogenesis, Regeneration and Trauma, Department of Surgery, University of Texas Southwestern, Dallas, TX, 75390, USA.
Aysel A FernandesDepartment of Orthopedics and Sports Medicine, University of Washington, Seattle, WA, 98195, USA.
Michael WoodardCenter for Organogenesis, Regeneration and Trauma, Department of Surgery, University of Texas Southwestern, Dallas, TX, 75390, USA.
Juhoon LeeDivision of Chemical Biology and Medicinal Chemistry, College of Pharmacy, University of Texas at Austin, Austin, TX, 78712, USA.
Sowmya RameshDepartment of Pathology, Johns Hopkins University, Baltimore, MD, 21218, USA.
Aaron W JamesDepartment of Pathology, Johns Hopkins University, Baltimore, MD, 21218, USA.ORCID http://orcid.org/0000-0002-2002-622X
David HudsonDepartment of Orthopedics and Sports Medicine, University of Washington, Seattle, WA, 98195, USA.
Kevin N DalbyDivision of Chemical Biology and Medicinal Chemistry, College of Pharmacy, University of Texas at Austin, Austin, TX, 78712, USA.
Lin XuQuantitative Biomedical Research Center, Peter O'Donnell Jr. School of Public Health, University of Texas Southwestern, Dallas, TX, 75390, USA.
Robert J TowerCenter for Organogenesis, Regeneration and Trauma, Department of Surgery, University of Texas Southwestern, Dallas, TX, 75390, USA.ORCID http://orcid.org/0000-0001-5856-5758
Benjamin LeviCenter for Organogenesis, Regeneration and Trauma, Department of Surgery, University of Texas Southwestern, Dallas, TX, 75390, USA. Benjamin.Levi@UTSouthwestern.edu.
Organogenesis (United States) · USJohns Hopkins University · USThe University of Texas at Austin · USThe University of Texas Southwestern Medical Center · USUniversity of Washington · USSouthwestern Medical Center · USUniversity of Michigan · US

Funding

UT Southwestern NORCP30DK127984 · NIDDK · UT SOUTHWESTERN MEDICAL CENTER · PI Jeffrey M Zigman · 2022 to 2026
$7.4M
Impacts of mechanosensation and matrix architecture on cell fate specification in traumatic heterotopic ossification - diversity supplementR01AR078324 · NIAMS · UT SOUTHWESTERN MEDICAL CENTER · PI LEVI, BENJAMIN · 2021 to 2025
$2.4M
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
NIAMS NIH HHS R01 AR071379NIAMS NIH HHS R01 AR078324NIDDK NIH HHS P30 DK127984
6 · The paper itself

Abstract

While hypoxic signaling has been shown to play a role in many cellular processes, its role in metabolism-linked extracellular matrix (ECM) organization and downstream processes of cell fate after musculoskeletal injury remains to be determined. Heterotopic ossification (HO) is a debilitating condition where abnormal bone formation occurs within extra-skeletal tissues. Hypoxia and hypoxia-inducible factor 1α (HIF-1α) activation have been shown to promote HO. However, the underlying molecular mechanisms by which the HIF-1α pathway in mesenchymal progenitor cells (MPCs) contributes to pathologic bone formation remain to be elucidated. Here, we used a proven mouse injury-induced HO model to investigate the role of HIF-1α on aberrant cell fate. Using single-cell RNA sequencing (scRNA-seq) and spatial transcriptomics analyses of the HO site, we found that collagen ECM organization is the most highly up-regulated biological process in MPCs. Zeugopod mesenchymal cell-specific deletion of Hif1α (Hoxa11-CreER

Indexed as

Ossification, HeterotopicOsteogenesisAnimalsCollagenDisease Models, AnimalExtracellular MatrixHypoxiaHypoxia-Inducible Factor 1, alpha SubunitMiceProcollagen-Lysine, 2-Oxoglutarate 5-DioxygenaseTranscription FactorsCollagenHif1a protein, mouseHypoxia-Inducible Factor 1, alpha Subunitlysyl hydroxylase 2, mouseProcollagen-Lysine, 2-Oxoglutarate 5-DioxygenaseTranscription Factors

Identifiers

PMID38472175
PMCPMC10933265
OpenAlexW4392716994

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.