Evidence map›Paper›PMID 39052334›Full record

ReviewJournal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research2024

Are osteoblasts multiple cell types? A new diversity in skeletal stem cells and their derivatives.

Seoyeon Bok, Jun Sun, Matthew B Greenblatt

Abstract readReview
In one paragraph

Review in Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing 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

4 citing papers in PubMed.

  1. Review
  2. Review
  3. Control of alveolar bone development, homeostasis, and socket healing by salt-inducible kinases.Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research · 2025
    Article
  4. 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

3 authors.

Seoyeon BokDepartment of Pathology and Laboratory Medicine, Weill Cornell Medical College, New York NY 10065, United States.
Jun SunDepartment of Pathology and Laboratory Medicine, Weill Cornell Medical College, New York NY 10065, United States.
Matthew B GreenblattDepartment of Pathology and Laboratory Medicine, Weill Cornell Medical College, New York NY 10065, United States.ORCID 0000-0001-9794-8532

Funding

Weill Cornell Medicine (WCM) SPORE in Prostate CancerP50CA211024 · NCI · WEILL MEDICAL COLL OF CORNELL UNIV · PI GUDAS, LORRAINE J · 2017 to 2021
$10.9M
Discovery of a stem cell driving breast cancer spine metastasesR01CA282815 · NCI · WEILL MEDICAL COLL OF CORNELL UNIV · PI Matthew Blake Greenblatt · 2024 to 2026
$2.4M
"Establishing Pathways for Endothelial Support of Bone Formation with SLIT3"R01AR075585 · NIAMS · WEILL MEDICAL COLL OF CORNELL UNIV · PI GREENBLATT, MATTHEW BLAKE · 2020 to 2024
$1.8M
A skeletal stem cell orchestrating limb regenerationR01HD115274 · NICHD · WEILL MEDICAL COLL OF CORNELL UNIV · PI Matthew Blake Greenblatt, Xu Yang · 2024 to 2026
$1.8M
Discovery of a stem cell governing vertebral physiologyR01AR083462 · NIAMS · WEILL MEDICAL COLL OF CORNELL UNIV · PI Matthew Blake Greenblatt · 2024 to 2026
$1.5M
Arthritis National Research FoundationBasic Science Research ProgramChildren's Tumor Foundation CTF-2023-01-005Marfan FoundationMary Kay Ash Foundation AwardMinistry of Education NRF-2021R1A6A3A14038667Mogam Science Scholarship FoundationNational Research Foundation of KoreaNCI NIH HHS P50 CA211024NCI NIH HHS R01 CA282815NIAMS NIH HHS R01 AR075585NIAMS NIH HHS R01 AR083462NICHD NIH HHS R01 HD115274NIH HHS R01HD115274Pershing Square Foundation
6 · The paper itself

Abstract

Only in the past decade have skeletal stem cells (SSCs), a cell type displaying formal evidence of stemness and serving as the ultimate origin of mature skeletal cell types such as osteoblasts, been defined. Here, we discuss a pair of recent reports that identify that SSCs do not represent a single cell type, but rather a family of related cells that each have characteristic anatomic locations and distinct functions tailored to the physiology of those sites. The distinct functional properties of these SSCs in turn provide a basis for the diseases of their respective locations. This concept emerges from one report identifying a distinct vertebral skeletal stem cell driving the high rate of breast cancer metastasis to the spine over other skeletal sites and a report identifying 2 SSCs in the calvaria that interact to mediate both physiologic calvarial mineralization and pathologic calvarial suture fusion in craniosynostosis. Despite displaying functional differences, these SSCs are each united by shared features including a shared series of surface markers and parallel differentiation hierarchies. We propose that this diversity at the level of SSCs in turn translates into a similar diversity at the level of mature skeletal cell types, including osteoblasts, with osteoblasts derived from different SSCs each displaying different functional and transcriptional characteristics reflecting their cell of origin. In this model, osteoblasts would represent not a single cell type, but rather a family of related cells each with distinct functions, paralleling the functional diversity in SSCs.

Indexed as

OsteoblastsStem CellsAnimalsBone and BonesCell DifferentiationHumansdevelopmental modelingosteoblastsotherstromal/stem cellstumor-induced bone disease

Identifiers

PMID39052334
PMCPMC11425698

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.