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

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 o...

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Autores principales: Ng, Pei Ying, Ribet, Amy B. P., Guo, Qiang, Mullin, Benjamin H., Tan, Jamie W. Y., Landao-Bassonga, Euphemie, Stephens, Sébastien, Chen, Kai, Yuan, Jinbo, Abudulai, Laila, Bollen, Maike, Nguyen, Edward T. T. T., Kular, Jasreen, Papadimitriou, John M., Søe, Kent, Teasdale, Rohan D., Xu, Jiake, Parton, Robert G., Takayanagi, Hiroshi, Pavlos, Nathan J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9945426/
https://www.ncbi.nlm.nih.gov/pubmed/36810735
http://dx.doi.org/10.1038/s41467-023-36484-2
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author Ng, Pei Ying
Ribet, Amy B. P.
Guo, Qiang
Mullin, Benjamin H.
Tan, Jamie W. Y.
Landao-Bassonga, Euphemie
Stephens, Sébastien
Chen, Kai
Yuan, Jinbo
Abudulai, Laila
Bollen, Maike
Nguyen, Edward T. T. T.
Kular, Jasreen
Papadimitriou, John M.
Søe, Kent
Teasdale, Rohan D.
Xu, Jiake
Parton, Robert G.
Takayanagi, Hiroshi
Pavlos, Nathan J.
author_facet Ng, Pei Ying
Ribet, Amy B. P.
Guo, Qiang
Mullin, Benjamin H.
Tan, Jamie W. Y.
Landao-Bassonga, Euphemie
Stephens, Sébastien
Chen, Kai
Yuan, Jinbo
Abudulai, Laila
Bollen, Maike
Nguyen, Edward T. T. T.
Kular, Jasreen
Papadimitriou, John M.
Søe, Kent
Teasdale, Rohan D.
Xu, Jiake
Parton, Robert G.
Takayanagi, Hiroshi
Pavlos, Nathan J.
author_sort Ng, Pei Ying
collection PubMed
description 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.
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spelling pubmed-99454262023-02-23 Sugar transporter Slc37a2 regulates bone metabolism in mice via a tubular lysosomal network in osteoclasts Ng, Pei Ying Ribet, Amy B. P. Guo, Qiang Mullin, Benjamin H. Tan, Jamie W. Y. Landao-Bassonga, Euphemie Stephens, Sébastien Chen, Kai Yuan, Jinbo Abudulai, Laila Bollen, Maike Nguyen, Edward T. T. T. Kular, Jasreen Papadimitriou, John M. Søe, Kent Teasdale, Rohan D. Xu, Jiake Parton, Robert G. Takayanagi, Hiroshi Pavlos, Nathan J. Nat Commun Article 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. Nature Publishing Group UK 2023-02-21 /pmc/articles/PMC9945426/ /pubmed/36810735 http://dx.doi.org/10.1038/s41467-023-36484-2 Text en © Crown 2023 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Ng, Pei Ying
Ribet, Amy B. P.
Guo, Qiang
Mullin, Benjamin H.
Tan, Jamie W. Y.
Landao-Bassonga, Euphemie
Stephens, Sébastien
Chen, Kai
Yuan, Jinbo
Abudulai, Laila
Bollen, Maike
Nguyen, Edward T. T. T.
Kular, Jasreen
Papadimitriou, John M.
Søe, Kent
Teasdale, Rohan D.
Xu, Jiake
Parton, Robert G.
Takayanagi, Hiroshi
Pavlos, Nathan J.
Sugar transporter Slc37a2 regulates bone metabolism in mice via a tubular lysosomal network in osteoclasts
title Sugar transporter Slc37a2 regulates bone metabolism in mice via a tubular lysosomal network in osteoclasts
title_full Sugar transporter Slc37a2 regulates bone metabolism in mice via a tubular lysosomal network in osteoclasts
title_fullStr Sugar transporter Slc37a2 regulates bone metabolism in mice via a tubular lysosomal network in osteoclasts
title_full_unstemmed Sugar transporter Slc37a2 regulates bone metabolism in mice via a tubular lysosomal network in osteoclasts
title_short Sugar transporter Slc37a2 regulates bone metabolism in mice via a tubular lysosomal network in osteoclasts
title_sort sugar transporter slc37a2 regulates bone metabolism in mice via a tubular lysosomal network in osteoclasts
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9945426/
https://www.ncbi.nlm.nih.gov/pubmed/36810735
http://dx.doi.org/10.1038/s41467-023-36484-2
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