Evidence map›Paper›PMID 36810735›Full record

ArticleNature communications2023

Sugar transporter Slc37a2 regulates bone metabolism in mice via a tubular lysosomal network in osteoclasts.

Pei Ying Ng, Amy B P Ribet, Qiang Guo, Benjamin H Mullin, Jamie W Y Tan, Euphemie Landao-Bassonga, Sébastien Stephens, Kai Chen, Jinbo Yuan, Laila Abudulai and 10 more

Open access · goldAbstract read
In one paragraph

Article in Nature communications, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed
5.1field-weighted citation impact, top 4% 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

22 citing papers in PubMed, 29 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Article
  5. Review
  6. Article
  7. Review
  8. Structural basis of glucose-6-phosphate transport by human SLC37A2.Nature structural & molecular biology · 2026
    Article
  9. Review
  10. Article
  11. Article
  12. Review
  13. Article
  14. Article
  15. Neurological glycogen storage diseases and emerging therapeutics.Neurotherapeutics : the journal of the American Society for Experimental NeuroTherapeutics · 2024
    Review
  16. Review
  17. Article
  18. Article
  19. Lysosomal biogenesis and function in osteoclasts: a comprehensive review.Frontiers in cell and developmental biology · 2024
    Review
  20. 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

20 authors at 7 institutions in 4 countries.

Pei Ying Ng *School of Biomedical Sciences, The University of Western Australia, Nedlands, WA, 6009, Australia.
Amy B P Ribet *School of Biomedical Sciences, The University of Western Australia, Nedlands, WA, 6009, Australia.ORCID 0000-0003-1168-6813
Qiang Guo *School of Biomedical Sciences, The University of Western Australia, Nedlands, WA, 6009, Australia.ORCID 0000-0002-4264-1290
Benjamin H MullinSchool of Biomedical Sciences, The University of Western Australia, Nedlands, WA, 6009, Australia.
Jamie W Y TanSchool of Biomedical Sciences, The University of Western Australia, Nedlands, WA, 6009, Australia.
Euphemie Landao-BassongaSchool of Biomedical Sciences, The University of Western Australia, Nedlands, WA, 6009, Australia.
Sébastien StephensSchool of Medicine and Dentistry, Griffith University, Southport, QLD, 4222, Australia.
Kai ChenSchool of Biomedical Sciences, The University of Western Australia, Nedlands, WA, 6009, Australia.
Jinbo YuanSchool of Biomedical Sciences, The University of Western Australia, Nedlands, WA, 6009, Australia.ORCID 0000-0002-6240-9333
Laila AbudulaiSchool of Biomedical Sciences, The University of Western Australia, Nedlands, WA, 6009, Australia.ORCID 0000-0003-4083-0343
Maike BollenCentre for Microscopy, Analysis and Characterisation, The University of Western Australia, Nedlands, WA, 6009, Australia.
Edward T T T NguyenSchool of Biomedical Sciences, The University of Western Australia, Nedlands, WA, 6009, Australia.ORCID 0000-0001-7625-7054
Jasreen KularSchool of Biomedical Sciences, The University of Western Australia, Nedlands, WA, 6009, Australia.
John M PapadimitriouPathWest Laboratory Medicine WA, Nedlands, WA, 6009, Australia.
Kent SøePathology Research Unit, Department of Clinical Research, University of Southern Denmark, Odense C, 5000, Denmark.ORCID 0000-0001-7402-314X
Rohan D TeasdaleSchool of Biomedical Sciences, The University of Queensland, Brisbane, QLD, 4072, Australia.
Jiake XuSchool of Biomedical Sciences, The University of Western Australia, Nedlands, WA, 6009, Australia.ORCID 0000-0003-2021-8309
Robert G PartonInstitute for Molecular Bioscience, The University of Queensland, Brisbane, QLD, 4072, Australia.ORCID 0000-0002-7494-5248
Hiroshi TakayanagiDepartment of Immunology, Graduate School of Medicine and Faculty of Medicine, The University of Tokyo, Tokyo, 113-0033, Japan.ORCID 0000-0002-1462-4127
Nathan J PavlosSchool of Biomedical Sciences, The University of Western Australia, Nedlands, WA, 6009, Australia. nathan.pavlos@uwa.edu.au.
The University of Western Australia · AUThe University of Queensland · AUCentral South University · CNGriffith University · AUPathwest Laboratory Medicine · AUThe University of Tokyo · JPUniversity of Southern Denmark · DK

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Osteoclasts are giant bone-digesting cells that harbor specialized lysosome-related organelles termed secretory lysosomes (SLs). SLs store cathepsin K and serve as a membrane precursor to the ruffled border, the osteoclast's 'resorptive apparatus'. Yet, the molecular composition and spatiotemporal organization of SLs remains incompletely understood. Here, using organelle-resolution proteomics, we identify member a2 of the solute carrier 37 family (Slc37a2) as a SL sugar transporter. We demonstrate in mice that Slc37a2 localizes to the SL limiting membrane and that these organelles adopt a hitherto unnoticed but dynamic tubular network in living osteoclasts that is required for bone digestion. Accordingly, mice lacking Slc37a2 accrue high bone mass owing to uncoupled bone metabolism and disturbances in SL export of monosaccharide sugars, a prerequisite for SL delivery to the bone-lining osteoclast plasma membrane. Thus, Slc37a2 is a physiological component of the osteoclast's unique secretory organelle and a potential therapeutic target for metabolic bone diseases.

Indexed as

Bone ResorptionOsteoclastsAnimalsBiological TransportBone and BonesCell MembraneLysosomesMice

Identifiers

PMID36810735
PMCPMC9945426
OpenAlexW4321455538

What OpenQuestion holds

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LicenceCC BY
Read underepoch 390

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.