Evidence map›Paper›PMID 32427356›Full record

ArticleJournal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research2020

Single-Cell RNA Sequencing of Calvarial and Long-Bone Endocortical Cells.

Ugur M Ayturk, Joseph P Scollan, Didem Goz Ayturk, Eun Sung Suh, Alexander Vesprey, Christina M Jacobsen, Paola Divieti Pajevic, Matthew L Warman

Open access · greenAbstract read
In one paragraph

Article in Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 47 papers.

0numbers the graph read from it
0cells of the map it votes in
47citing papers in PubMed
3.0field-weighted citation impact, top 8% 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

47 citing papers in PubMed, 56 citations in OpenAlex.

  1. Article
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  6. Conditional deletion ofFrontiers in cell and developmental biology · 2026
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  11. Modeling of skeletal development and diseases using human pluripotent stem cells.Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research · 2024
    Review
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  19. Multi-organ phenotypes in mice lacking latent TGFβ binding protein 2 (LTBP2).Developmental dynamics : an official publication of the American Association of Anatomists · 2024
    Review
  20. 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

8 authors at 4 institutions in 2 countries.

Ugur M AyturkMusculoskeletal Integrity Program, Hospital for Special Surgery, New York, NY, USA.ORCID 0000-0001-6625-2743
Joseph P ScollanDepartment of Orthopaedic Surgery, Cleveland Clinic Foundation, Cleveland, OH, USA.
Didem Goz AyturkMusculoskeletal Integrity Program, Hospital for Special Surgery, New York, NY, USA.
Eun Sung SuhMusculoskeletal Integrity Program, Hospital for Special Surgery, New York, NY, USA.
Alexander VespreyMusculoskeletal Integrity Program, Hospital for Special Surgery, New York, NY, USA.
Christina M JacobsenDepartment of Orthopaedic Surgery, Boston Children's Hospital, Boston, MA, USA.
Paola Divieti PajevicDepartment of Translational Dental Medicine, Boston University Goldman School of Dental Medicine, Boston, MA, USA.ORCID 0000-0001-9853-9837
Matthew L WarmanDepartment of Orthopaedic Surgery, Boston Children's Hospital, Boston, MA, USA.ORCID 0000-0003-2020-3449
Hospital for Special Surgery · USBoston Children's Hospital · USBoston University · USCleveland Clinic · US

Funding

Lrp5 signaling in bone mechanotransduction and metabolismR01AR053237 · NIAMS · INDIANA UNIV-PURDUE UNIV AT INDIANAPOLIS · PI ALEXANDER G ROBLING, Matthew L Warman · 2005 to 2026
$9.4M
Comprehensive Training Program in Musculoskeletal ResearchT32AR065971 · NIAMS · INDIANA UNIVERSITY INDIANAPOLIS · PI ALEXANDER G ROBLING · 2015 to 2026
$4.4M
Skeletal Phenotyping CoreP30AR066261 · NIAMS · MASSACHUSETTS GENERAL HOSPITAL · PI KRONENBERG, HENRY M. · 2014 to 2018
$3.5M
The LRP5 Pathway and Osteoblast Function In Osteogenesis ImperfectaR01AR071342 · NIAMS · BOSTON CHILDREN'S HOSPITAL · PI JACOBSEN, CHRISTINA MARIE · 2018 to 2022
$3.0M
Non-heritable genetic diseases of the skeletal system: Pathogenesis and TreatmentR01AR064231 · NIAMS · BOSTON CHILDREN'S HOSPITAL · PI WARMAN, MATTHEW L · 2014 to 2018
$1.9M
The Efficacy of combination therapy in Osteogenesis ImperfectaR21AR067388 · NIAMS · BOSTON CHILDREN'S HOSPITAL · PI WARMAN, MATTHEW L · 2015 to 2016
$428k
NIAMS NIH HHS P30 AR066261NIAMS NIH HHS R01 AR053237NIAMS NIH HHS R01 AR064231NIAMS NIH HHS R01 AR071342NIAMS NIH HHS R21 AR067388NIAMS NIH HHS T32 AR065971NIH HHS P30 AR066261NIH HHS R01 AR053237NIH HHS R01 AR064231NIH HHS R01 AR071342NIH HHS R21AR067388
6 · The paper itself

Abstract

Single-cell RNA sequencing (scRNA-Seq) is emerging as a powerful technology to examine transcriptomes of individual cells. We determined whether scRNA-Seq could be used to detect the effect of environmental and pharmacologic perturbations on osteoblasts. We began with a commonly used in vitro system in which freshly isolated neonatal mouse calvarial cells are expanded and induced to produce a mineralized matrix. We used scRNA-Seq to compare the relative cell type abundances and the transcriptomes of freshly isolated cells to those that had been cultured for 12 days in vitro. We observed that the percentage of macrophage-like cells increased from 6% in freshly isolated calvarial cells to 34% in cultured cells. We also found that Bglap transcripts were abundant in freshly isolated osteoblasts but nearly undetectable in the cultured calvarial cells. Thus, scRNA-Seq revealed significant differences between heterogeneity of cells in vivo and in vitro. We next performed scRNA-Seq on freshly recovered long bone endocortical cells from mice that received either vehicle or sclerostin-neutralizing antibody for 1 week. We were unable to detect significant changes in bone anabolism-associated transcripts in immature and mature osteoblasts recovered from mice treated with sclerostin-neutralizing antibody; this might be a consequence of being underpowered to detect modest changes in gene expression, because only 7% of the sequenced endocortical cells were osteoblasts and a limited portion of their transcriptomes were sampled. We conclude that scRNA-Seq can detect changes in cell abundance, identity, and gene expression in skeletally derived cells. In order to detect modest changes in osteoblast gene expression at the single-cell level in the appendicular skeleton, larger numbers of osteoblasts from endocortical bone are required. © 2020 American Society for Bone and Mineral Research.

Indexed as

OsteoblastsOsteocytesSequence Analysis, RNAAnimalsGene Expression ProfilingMiceSingle-Cell AnalysisTranscriptomeANIMAL MODELSCELLS OF BONEOSTEOBLASTSSTATISTICAL METHODSSTROMAL/STEM CELLS

Identifiers

PMID32427356
PMCPMC8265023
OpenAlexW3028316745

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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.