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Endoplasmic reticulum mediates mitochondrial transfer within the osteocyte dendritic network
Mitochondrial transfer plays a crucial role in the regulation of tissue homeostasis and resistance to cancer chemotherapy. Osteocytes have interconnecting dendritic networks and are a model to investigate its mechanism. We have demonstrated, in primary murine osteocytes with photoactivatable mitocho...
Autores principales: | , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Association for the Advancement of Science
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6867880/ https://www.ncbi.nlm.nih.gov/pubmed/31799389 http://dx.doi.org/10.1126/sciadv.aaw7215 |
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author | Gao, Junjie Qin, An Liu, Delin Ruan, Rui Wang, Qiyang Yuan, Jun Cheng, Tak Sum Filipovska, Aleksandra Papadimitriou, J. M. Dai, Kerong Jiang, Qing Gao, Xiang Feng, Jian Q. Takayanagi, Hiroshi Zhang, Changqing Zheng, Ming H. |
author_facet | Gao, Junjie Qin, An Liu, Delin Ruan, Rui Wang, Qiyang Yuan, Jun Cheng, Tak Sum Filipovska, Aleksandra Papadimitriou, J. M. Dai, Kerong Jiang, Qing Gao, Xiang Feng, Jian Q. Takayanagi, Hiroshi Zhang, Changqing Zheng, Ming H. |
author_sort | Gao, Junjie |
collection | PubMed |
description | Mitochondrial transfer plays a crucial role in the regulation of tissue homeostasis and resistance to cancer chemotherapy. Osteocytes have interconnecting dendritic networks and are a model to investigate its mechanism. We have demonstrated, in primary murine osteocytes with photoactivatable mitochondria (PhAM)(floxed) and in MLO-Y4 cells, mitochondrial transfer in the dendritic networks visualized by high-resolution confocal imaging. Normal osteocytes transferred mitochondria to adjacent metabolically stressed osteocytes and restored their metabolic function. The coordinated movement and transfer of mitochondria within the dendritic network rely on contact between the endoplasmic reticulum (ER) and mitochondria. Mitofusin 2 (Mfn2), a GTPase that tethers ER to mitochondria, predominantly mediates the transfer. A decline in Mfn2 expression with age occurs concomitantly with both impaired mitochondrial distribution and transfer in the osteocyte dendritic network. These data show a previously unknown function of ER-mitochondrial contact in mediating mitochondrial transfer and provide a mechanism to explain the homeostasis of osteocytes. |
format | Online Article Text |
id | pubmed-6867880 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | American Association for the Advancement of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-68678802019-12-03 Endoplasmic reticulum mediates mitochondrial transfer within the osteocyte dendritic network Gao, Junjie Qin, An Liu, Delin Ruan, Rui Wang, Qiyang Yuan, Jun Cheng, Tak Sum Filipovska, Aleksandra Papadimitriou, J. M. Dai, Kerong Jiang, Qing Gao, Xiang Feng, Jian Q. Takayanagi, Hiroshi Zhang, Changqing Zheng, Ming H. Sci Adv Research Articles Mitochondrial transfer plays a crucial role in the regulation of tissue homeostasis and resistance to cancer chemotherapy. Osteocytes have interconnecting dendritic networks and are a model to investigate its mechanism. We have demonstrated, in primary murine osteocytes with photoactivatable mitochondria (PhAM)(floxed) and in MLO-Y4 cells, mitochondrial transfer in the dendritic networks visualized by high-resolution confocal imaging. Normal osteocytes transferred mitochondria to adjacent metabolically stressed osteocytes and restored their metabolic function. The coordinated movement and transfer of mitochondria within the dendritic network rely on contact between the endoplasmic reticulum (ER) and mitochondria. Mitofusin 2 (Mfn2), a GTPase that tethers ER to mitochondria, predominantly mediates the transfer. A decline in Mfn2 expression with age occurs concomitantly with both impaired mitochondrial distribution and transfer in the osteocyte dendritic network. These data show a previously unknown function of ER-mitochondrial contact in mediating mitochondrial transfer and provide a mechanism to explain the homeostasis of osteocytes. American Association for the Advancement of Science 2019-11-20 /pmc/articles/PMC6867880/ /pubmed/31799389 http://dx.doi.org/10.1126/sciadv.aaw7215 Text en Copyright © 2019 The Authors, some rights reserved; exclusive licensee American Association for the Advancement of Science. No claim to original U.S. Government Works. Distributed under a Creative Commons Attribution NonCommercial License 4.0 (CC BY-NC). http://creativecommons.org/licenses/by-nc/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution-NonCommercial license (http://creativecommons.org/licenses/by-nc/4.0/) , which permits use, distribution, and reproduction in any medium, so long as the resultant use is not for commercial advantage and provided the original work is properly cited. |
spellingShingle | Research Articles Gao, Junjie Qin, An Liu, Delin Ruan, Rui Wang, Qiyang Yuan, Jun Cheng, Tak Sum Filipovska, Aleksandra Papadimitriou, J. M. Dai, Kerong Jiang, Qing Gao, Xiang Feng, Jian Q. Takayanagi, Hiroshi Zhang, Changqing Zheng, Ming H. Endoplasmic reticulum mediates mitochondrial transfer within the osteocyte dendritic network |
title | Endoplasmic reticulum mediates mitochondrial transfer within the osteocyte dendritic network |
title_full | Endoplasmic reticulum mediates mitochondrial transfer within the osteocyte dendritic network |
title_fullStr | Endoplasmic reticulum mediates mitochondrial transfer within the osteocyte dendritic network |
title_full_unstemmed | Endoplasmic reticulum mediates mitochondrial transfer within the osteocyte dendritic network |
title_short | Endoplasmic reticulum mediates mitochondrial transfer within the osteocyte dendritic network |
title_sort | endoplasmic reticulum mediates mitochondrial transfer within the osteocyte dendritic network |
topic | Research Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6867880/ https://www.ncbi.nlm.nih.gov/pubmed/31799389 http://dx.doi.org/10.1126/sciadv.aaw7215 |
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