Evidence map›Paper›PMID 22074949›Full record

ArticleMolecular endocrinology (Baltimore, Md.)2012

BMP3 suppresses osteoblast differentiation of bone marrow stromal cells via interaction with Acvr2b.

Shoichiro Kokabu, Laura Gamer, Karen Cox, Jonathan Lowery, Kunikazu Tsuji, Regina Raz, Aris Economides, Takenobu Katagiri, Vicki Rosen

Open access · greenAbstract read
In one paragraph

Article in Molecular endocrinology (Baltimore, Md.), 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 63 papers.

0numbers the graph read from it
0cells of the map it votes in
63citing papers in PubMed
3.1field-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

63 citing papers in PubMed, 118 citations in OpenAlex.

  1. Review
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  7. American journal of translational research · 2024
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  16. BMP3 Affects Cortical and Trabecular Long Bone Development in Mice.International journal of molecular sciences · 2022
    Article
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  20. Review

3 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

9 authors at 4 institutions in 2 countries.

Shoichiro KokabuDepartment of Developmental Biology, Harvard School of Dental Medicine, Boston, Massachusetts 02115, USA.
Laura Gamer
Karen Cox
Jonathan Lowery
Kunikazu Tsuji
Regina Raz
Aris Economides
Takenobu Katagiri
Vicki Rosen
Harvard University · USRegeneron (United States) · USSaitama Medical University · JPTokyo Medical and Dental University · JP

Funding

BMP-3 Signaling in the Formation and Regulation of BoneR01AR050174 · NIAMS · HARVARD UNIVERSITY (MEDICAL SCHOOL) · PI ROSEN, VICKI · 2004 to 2009
$2.3M
NIAMS NIH HHS AR50174NIAMS NIH HHS R01 AR050174
6 · The paper itself

Abstract

Enhancing bone morphogenetic protein (BMP) signaling increases bone formation in a variety of settings that target bone repair. However, the role of BMP in the maintenance of adult bone mass is not well understood. Targeted disruption of BMP3 in mice results in increased trabecular bone formation, whereas transgenic overexpression of BMP3 in skeletal cells leads to spontaneous fracture, consistent with BMP3 having a negative role in bone mass regulation. Here we investigate the importance of BMP3 as a mediator of BMP signaling in the adult skeleton. We find that osteoblasts (OBL) and osteocytes are the source of BMP3 in adult bone. Using in vitro cultures of primary bone marrow stromal cells, we show that overexpression of BMP3 suppresses OBL differentiation, whereas loss of BMP3 increases colony-forming unit fibroblasts and colony-forming unit OBL. The ability of BMP3 to affect OBL differentiation is due to its interaction with activin receptor type 2b (Acvr2b) because knockdown of endogenous Acvr2b in bone marrow stromal cells reduces the suppressive effect of BMP3 on OBL differentiation. These findings best fit a model in which BMP3, produced by mature bone cells, acts to reduce BMP signaling through Acvr2b in skeletal progenitor cells, limiting their differentiation to mature OBL. Our data further support the idea that endogenous BMPs have a physiological role in regulating adult bone mass.

Indexed as

OsteogenesisActivin Receptors, Type IIAnimalsBone Marrow CellsBone Morphogenetic Protein 3Cell DifferentiationCell LineGene Knock-In TechniquesMiceMice, Inbred C57BLMice, KnockoutOsteoblastsOsteocytesRNA InterferenceRNA, Small InterferingSignal TransductionActivin Receptors, Type IIactivin receptor type II-BBmp3 protein, mouseBone Morphogenetic Protein 3RNA, Small InterferingSmad Proteins

Identifiers

PMID22074949
PMCPMC3248326
OpenAlexW1970791930

What OpenQuestion holds

Textmetadata
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.