Evidence map›Paper›PMID 39528700›Full record

ArticleNature cell biology2024

Specialized post-arterial capillaries facilitate adult bone remodelling.

Vishal Mohanakrishnan, Kishor K Sivaraj, Hyun-Woo Jeong, Esther Bovay, Backialakshmi Dharmalingam, M Gabriele Bixel, Van Vuong Dinh, Milena Petkova, Isidora Paredes Ugarte, Yi-Tong Kuo and 11 more

Abstract read
In one paragraph

Article in Nature cell biology, 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
–field-weighted citation impact
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.

  1. Article
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  9. VEGF-D-induced intraosseous lymphangiogenesis drives site-specific heterotopic bone resorption.Proceedings of the National Academy of Sciences of the United States of America · 2026
    Article
  10. Article
  11. Development-based In Vivo Bioreactor Strategy for Challenging Senescent Bone Reconstruction.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2026
    Article
  12. Article
  13. Article
  14. Article
  15. Targeting Arterial Dysfunction in Cardiovascular Disease Using Stem Cell-Based Therapies.FASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2026
    Review
  16. Article
  17. Article
  18. Review
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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

21 authors.

Vishal MohanakrishnanMax Planck Institute for Molecular Biomedicine, Department of Tissue Morphogenesis, Münster, Germany.ORCID 0000-0003-0976-9230
Kishor K SivarajMax Planck Institute for Molecular Biomedicine, Department of Tissue Morphogenesis, Münster, Germany.ORCID 0000-0002-5321-3400
Hyun-Woo JeongMax Planck Institute for Molecular Biomedicine, Single Cell Multi-Omics Laboratory, Münster, Germany.ORCID 0000-0002-6976-6739
Esther BovayMax Planck Institute for Molecular Biomedicine, Department of Tissue Morphogenesis, Münster, Germany.
Backialakshmi DharmalingamMax Planck Institute for Molecular Biomedicine, Department of Tissue Morphogenesis, Münster, Germany.ORCID 0000-0003-2922-0501
M Gabriele BixelMax Planck Institute for Molecular Biomedicine, Department of Tissue Morphogenesis, Münster, Germany.ORCID 0000-0001-8656-8075
Van Vuong DinhMax Planck Institute for Molecular Biomedicine, Department of Tissue Morphogenesis, Münster, Germany.
Milena PetkovaDepartment of Immunology, Genetics, and Pathology, Uppsala University, Uppsala, Sweden.
Isidora Paredes UgarteMax Planck Institute for Molecular Biomedicine, Department of Tissue Morphogenesis, Münster, Germany.
Yi-Tong KuoMax Planck Institute for Molecular Biomedicine, Department of Tissue Morphogenesis, Münster, Germany.
Malarvizhi GurusamyMax Planck Institute for Molecular Biomedicine, Department of Tissue Morphogenesis, Münster, Germany.
Brian RaftreyDepartment of Biology, Stanford University, Stanford, CA, USA.
Nelson Tsz Long ChuDepartment of Physiology and Pharmacology, Karolinska Institute, Stockholm, Sweden.
Soumyashree DasDepartment of Biology, Stanford University, Stanford, CA, USA.
Pamela E Rios CoronadoDepartment of Biology, Stanford University, Stanford, CA, USA.
Martin StehlingMax Planck Institute for Molecular Biomedicine, Flow Cytometry Unit, Münster, Germany.
Lars SävendahlDepartment of Women's and Children's Health, Karolinska Institutet and Pediatric Endocrinology Unit, Karolinska University Hospital, Stockholm, Sweden.ORCID 0000-0003-1067-4976
Andrei S ChaginDepartment of Physiology and Pharmacology, Karolinska Institute, Stockholm, Sweden.ORCID 0000-0002-2696-5850
Taija MäkinenDepartment of Immunology, Genetics, and Pathology, Uppsala University, Uppsala, Sweden.ORCID 0000-0002-9338-1257
Kristy Red-HorseDepartment of Biology, Stanford University, Stanford, CA, USA.ORCID 0000-0003-1541-601X
Ralf H AdamsMax Planck Institute for Molecular Biomedicine, Department of Tissue Morphogenesis, Münster, Germany. ralf.adams@mpi-muenster.mpg.de.ORCID 0000-0003-3031-7677

Funding

Supplement to Enhance Wellness and Resiliency in the Graduate EnvironmentT32GM007276 · NIGMS · STANFORD UNIVERSITY · PI MORRISON, ASHBY J. · 1985 to 2023
$32.9M
Mechanotransduction and transcriptional regulation during artery developmentR01HL128503 · NHLBI · STANFORD UNIVERSITY · PI Mary Red-Horse · 2015 to 2026
$5.8M
Deutsche Forschungsgemeinschaft (German Research Foundation) CRC 1366EC | EU Framework Programme for Research and Innovation H2020 | H2020 Priority Excellent Science | H2020 European Research Council (H2020 Excellent Science - European Research Council) AdG 101139772Foundation for the National Institutes of Health (Foundation for the National Institutes of Health, Inc.) R01-HL128503Göteborgs Universitet (University of Gothenburg) ALFGBG-966178Knut och Alice Wallenbergs Stiftelse (Knut and Alice Wallenberg Foundation) 2020.0057NHLBI NIH HHS R01 HL128503NIGMS NIH HHS T32 GM007276U.S. Department of Health & Human Services | NIH | National Institute of General Medical Sciences (NIGMS) DGE-1656518U.S. Department of Health & Human Services | NIH | National Institute of General Medical Sciences (NIGMS) T32GM007276Vetenskapsrådet (Swedish Research Council) 2020-02298Vetenskapsrådet (Swedish Research Council) 2020-02692
6 · The paper itself

Abstract

The vasculature of the skeletal system is crucial for bone formation, homoeostasis and fracture repair, yet the diversity and specialization of bone-associated vessels remain poorly understood. Here we identify a specialized type of post-arterial capillary, termed type R, involved in bone remodelling. Type R capillaries emerge during adolescence around trabecular bone, possess a distinct morphology and molecular profile, and are associated with osteoprogenitors and bone-resorbing osteoclasts. Endothelial cell-specific overexpression of the transcription factor DACH1 in postnatal mice induces a strong increase in arteries and type R capillaries, leading to local metabolic changes and enabling trabecular bone formation in normally highly hypoxic areas of the diaphysis. Indicating potential clinical relevance of type R capillaries, these vessels respond to anti-osteoporosis treatments and emerge during ageing inside porous structures that are known to weaken compact bone. Our work outlines fundamental principles of vessel specialization in the developing, adult and ageing skeletal system.

Indexed as

Bone RemodelingCapillariesAgingAnimalsArteriesBone and BonesCancellous BoneEndothelial CellsFemaleHumansMaleMiceMice, Inbred C57BLMice, TransgenicNeovascularization, PhysiologicOsteoclasts

Identifiers

PMID39528700
PMCPMC11628402

What OpenQuestion holds

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LicenceCC BY
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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.