Evidence map›Paper›PMID 32927921›Full record

ReviewCells2020

Osteoblast-Osteoclast Communication and Bone Homeostasis.

Jung-Min Kim, Chujiao Lin, Zheni Stavre, Matthew B Greenblatt, Jae-Hyuck Shim

Open access · goldAbstract readReview
In one paragraph

Review in Cells, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 611 papers, 4 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
611citing papers in PubMed, 4 pooled it
41.9field-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

611 citing papers in PubMed, 4 syntheses or guidelines pooled it, 1,071 citations in OpenAlex.

  1. Pooled it
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  8. Bone health in diabetes mellitus.Reviews in endocrine & metabolic disorders · 2026
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551 more citing papers are in PubMed but not listed here.

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

5 authors at 2 institutions in 1 country.

Jung-Min KimDivision of Rheumatology, Department of Medicine, University of Massachusetts Medical School, Worcester, MA 01605, USA.
Chujiao LinDivision of Rheumatology, Department of Medicine, University of Massachusetts Medical School, Worcester, MA 01605, USA.
Zheni StavreDivision of Rheumatology, Department of Medicine, University of Massachusetts Medical School, Worcester, MA 01605, USA.
Matthew B GreenblattDepartment of Pathology and Laboratory Medicine, Weill Cornell Medical College, New York, NY 10065, USA.
Jae-Hyuck ShimDivision of Rheumatology, Department of Medicine, University of Massachusetts Medical School, Worcester, MA 01605, USA.ORCID 0000-0002-4947-3293
University of Massachusetts Chan Medical School · USCornell University · US

Funding

Modulation of Bone Formation by SHN3DP5OD021351 · OD · WEILL MEDICAL COLL OF CORNELL UNIV · PI GREENBLATT, MATTHEW BLAKE · 2015 to 2019
$2.1M
Identification of novel regulators governing osteoclast-osteoblast couplingR01AR068983 · NIAMS · WEILL MEDICAL COLL OF CORNELL UNIV · PI SHIM, JAE-HYUCK · 2016 to 2020
$1.9M
"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
NIAMS NIH HHS R01 AR068983NIAMS NIH HHS R01 AR075585NIH HHS DP5 OD021351
6 · The paper itself

Abstract

Bone remodeling is tightly regulated by a cross-talk between bone-forming osteoblasts and bone-resorbing osteoclasts. Osteoblasts and osteoclasts communicate with each other to regulate cellular behavior, survival and differentiation through direct cell-to-cell contact or through secretory proteins. A direct interaction between osteoblasts and osteoclasts allows bidirectional transduction of activation signals through EFNB2-EPHB4, FASL-FAS or SEMA3A-NRP1, regulating differentiation and survival of osteoblasts or osteoclasts. Alternatively, osteoblasts produce a range of different secretory molecules, including M-CSF, RANKL/OPG, WNT5A, and WNT16, that promote or suppress osteoclast differentiation and development. Osteoclasts also influence osteoblast formation and differentiation through secretion of soluble factors, including S1P, SEMA4D, CTHRC1 and C3. Here we review the current knowledge regarding membrane bound- and soluble factors governing cross-talk between osteoblasts and osteoclasts.

Indexed as

Bone and BonesBone RemodelingCell CommunicationCell DifferentiationHomeostasisHumansOsteoblastsOsteoclastsSignal Transductionbonebone remodelingosteoblastosteoclast

Identifiers

PMID32927921
PMCPMC7564526
OpenAlexW3083952170

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.