Evidence map›Paper›PMID 34213032›Full record

ReviewJournal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research2021

The diverse origin of bone-forming osteoblasts.

Toshihide Mizoguchi, Noriaki Ono

Open access · bronzeAbstract readReview
In one paragraph

Review in Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 77 papers.

0numbers the graph read from it
0cells of the map it votes in
77citing papers in PubMed
4.2field-weighted citation impact, top 5% 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

77 citing papers in PubMed, 132 citations in OpenAlex.

  1. Review
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  11. CRISPR-mediated conditional mutagenesis ofbioRxiv : the preprint server for biology · 2026
    Article
  12. Article
  13. Review
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  15. Review
  16. Cell fusion in osteoclastogenesis.Biochemical Society transactions · 2025
    Review
  17. Article
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  19. Review
  20. Intracellular survival ofVirulence · 2025
    Review

17 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

2 authors at 2 institutions in 2 countries.

Toshihide MizoguchiOral Health Science Center, Tokyo Dental College, Tokyo, Japan.ORCID 0000-0001-9910-6419
Noriaki OnoUniversity of Texas Health Science Center at Houston School of Dentistry, Houston, TX, USA.ORCID 0000-0002-3771-8230
The University of Texas Health Science Center at Houston · USTokyo Dental College · JP

Funding

Craniofacial skeletal cell lineage plasticity for reconstituting stem cells and their nichesR01DE030630 · NIDCR · UNIVERSITY OF TEXAS HLTH SCI CTR HOUSTON · PI ONO, NORIAKI, ONO, WANIDA · 2021 to 2025
$2.2M
Dynamics and Regulations of Bone Stem Cells in VivoR01DE026666 · NIDCR · UNIVERSITY OF TEXAS HLTH SCI CTR HOUSTON · PI ONO, NORIAKI · 2018 to 2022
$2.1M
Dental Follicle: A Central Regulator of Tooth Eruption and Root FormationR03DE027421 · NIDCR · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI ONO, WANIDA · 2018 to 2019
$312k
NIDCR NIH HHS R01 DE026666NIDCR NIH HHS R01 DE030630NIDCR NIH HHS R03 DE027421
6 · The paper itself

Abstract

Osteoblasts are the only cells that can give rise to bones in vertebrates. Thus, one of the most important functions of these metabolically active cells is mineralized matrix production. Because osteoblasts have a limited lifespan, they must be constantly replenished by preosteoblasts, their immediate precursors. Because disruption of the regulation of bone-forming osteoblasts results in a variety of bone diseases, a better understanding of the origin of these cells by defining the mechanisms of bone development, remodeling, and regeneration is central to the development of novel therapeutic approaches. In recent years, substantial new insights into the origin of osteoblasts-largely owing to rapid technological advances in murine lineage-tracing approaches and other single-cell technologies-have been obtained. Collectively, these findings indicate that osteoblasts involved in bone formation under various physiological, pathological, and therapeutic conditions can be obtained from numerous sources. The origins of osteoblasts include, but are not limited to, chondrocytes in the growth plate, stromal cells in the bone marrow, quiescent bone-lining cells on the bone surface, and specialized fibroblasts in the craniofacial structures, such as sutures and periodontal ligaments. Because osteoblasts can be generated from local cellular sources, bones can flexibly respond to regenerative and anabolic cues. However, whether osteoblasts derived from different cellular sources have distinct functions remains to be investigated. Currently, we are at the initial stage to aptly unravel the incredible diversity of the origins of bone-forming osteoblasts. © 2021 American Society for Bone and Mineral Research (ASBMR).

Indexed as

Growth PlateOsteoblastsAnimalsBone and BonesBone DevelopmentMiceOsteogenesisBONE DEVELOPMENTBONE MARROW STROMAL CELLSBONE REGENERATIONCHONDROCYTESOSTEOBLASTSSKELETAL STEM CELLS

Identifiers

PMID34213032
PMCPMC8338797
OpenAlexW3173562351

What OpenQuestion holds

Textmetadata
LicenceTDM
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.