Evidence map›Paper›PMID 30158637›Full record

ArticleScientific reports2018

Septins are critical regulators of osteoclastic bone resorption.

Anaïs M J Møller, Ernst-Martin Füchtbauer, Annemarie Brüel, Thomas L Andersen, Xenia G Borggaard, Nathan J Pavlos, Jesper S Thomsen, Finn S Pedersen, Jean-Marie Delaisse, Kent Søe

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
1.4field-weighted citation impact, top 18% 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

14 citing papers in PubMed, 25 citations in OpenAlex.

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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

10 authors at 3 institutions in 2 countries.

Anaïs M J MøllerDepartment of Clinical Cell Biology, Vejle Hospital/Lillebaelt Hospital, Institute of Regional Health Research, University of Southern Denmark, Beriderbakken 4, 7100, Vejle, Denmark.
Ernst-Martin FüchtbauerDepartment of Molecular Biology and Genetics, Aarhus University, 8000, Aarhus, Denmark.ORCID 0000-0002-9320-7195
Annemarie BrüelDepartment of Biomedicine, Aarhus University, 8000, Aarhus, Denmark.
Thomas L AndersenDepartment of Clinical Cell Biology, Vejle Hospital/Lillebaelt Hospital, Institute of Regional Health Research, University of Southern Denmark, Beriderbakken 4, 7100, Vejle, Denmark.
Xenia G BorggaardDepartment of Clinical Cell Biology, Vejle Hospital/Lillebaelt Hospital, Institute of Regional Health Research, University of Southern Denmark, Beriderbakken 4, 7100, Vejle, Denmark.
Nathan J PavlosCellular Orthopaedic Laboratory, School of Biomedical Sciences, University of Western Australia, Nedlands, 6009, Australia.
Jesper S ThomsenDepartment of Biomedicine, Aarhus University, 8000, Aarhus, Denmark.
Finn S PedersenDepartment of Molecular Biology and Genetics, Aarhus University, 8000, Aarhus, Denmark.
Jean-Marie DelaisseDepartment of Clinical Cell Biology, Vejle Hospital/Lillebaelt Hospital, Institute of Regional Health Research, University of Southern Denmark, Beriderbakken 4, 7100, Vejle, Denmark.
Kent SøeDepartment of Clinical Cell Biology, Vejle Hospital/Lillebaelt Hospital, Institute of Regional Health Research, University of Southern Denmark, Beriderbakken 4, 7100, Vejle, Denmark. kent.soee@rsyd.dk.ORCID 0000-0001-7402-314X
University of Southern Denmark · DKAarhus University · DKThe University of Western Australia · AU

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Septins are known to play key roles in supporting cytoskeletal stability, vesicular transport, endo-/exocytosis, stabilizing cellular membranes and forming diffusion barriers. Their function in mammalian cells is poorly investigated. The osteoclast offers an interesting tool to investigate septins because all cellular activities septins were reported to be involved in are critical for osteoclasts. However, the existence of septins in osteoclasts has not even been reported. Here we show that the SEPT9 gene and Septin 9 (SEPT9) protein are expressed and synthesized during differentiation of human osteoclasts. Pharmacological stabilization of septin filaments dose dependently inhibits bone resorption of human osteoclasts in vitro suggesting a role for septins in bone resorption. Attesting to this, conditional deletion of Sept9 in mice leads to elevated levels of trabecular bone and diminished femoral growth in vivo. Finally, systematic interrogation of the spatial organization of SEPT9 by confocal microscopy reveals that SEPT9 is closely associated to the structures known to be critical for osteoclast activity. We propose that septins in general and SEPT9 in particular play a previously unappreciated role in osteoclastic bone resorption.

Indexed as

Bone ResorptionCell DifferentiationAnimalsCells, CulturedFemurGene Knockdown TechniquesHumansMiceOsteoclastsSeptinsseptin 9, mouseSEPTIN9 protein, humanSeptins

Identifiers

PMID30158637
PMCPMC6115361
OpenAlexW2888687068

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.