Cargando…

Disruption of ER−mitochondria signalling in fronto-temporal dementia and related amyotrophic lateral sclerosis

Fronto-temporal dementia (FTD) and amyotrophic lateral sclerosis (ALS) are two related and incurable neurodegenerative diseases. Features of these diseases include pathological protein inclusions in affected neurons with TAR DNA-binding protein 43 (TDP-43), dipeptide repeat proteins derived from the...

Descripción completa

Detalles Bibliográficos
Autores principales: Lau, Dawn H. W., Hartopp, Naomi, Welsh, Natalie J., Mueller, Sarah, Glennon, Elizabeth B., Mórotz, Gábor M., Annibali, Ambra, Gomez-Suaga, Patricia, Stoica, Radu, Paillusson, Sebastien, Miller, Christopher C. J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5832427/
https://www.ncbi.nlm.nih.gov/pubmed/29491392
http://dx.doi.org/10.1038/s41419-017-0022-7
_version_ 1783303321274023936
author Lau, Dawn H. W.
Hartopp, Naomi
Welsh, Natalie J.
Mueller, Sarah
Glennon, Elizabeth B.
Mórotz, Gábor M.
Annibali, Ambra
Gomez-Suaga, Patricia
Stoica, Radu
Paillusson, Sebastien
Miller, Christopher C. J.
author_facet Lau, Dawn H. W.
Hartopp, Naomi
Welsh, Natalie J.
Mueller, Sarah
Glennon, Elizabeth B.
Mórotz, Gábor M.
Annibali, Ambra
Gomez-Suaga, Patricia
Stoica, Radu
Paillusson, Sebastien
Miller, Christopher C. J.
author_sort Lau, Dawn H. W.
collection PubMed
description Fronto-temporal dementia (FTD) and amyotrophic lateral sclerosis (ALS) are two related and incurable neurodegenerative diseases. Features of these diseases include pathological protein inclusions in affected neurons with TAR DNA-binding protein 43 (TDP-43), dipeptide repeat proteins derived from the C9ORF72 gene, and fused in sarcoma (FUS) representing major constituent proteins in these inclusions. Mutations in C9ORF72 and the genes encoding TDP-43 and FUS cause familial forms of FTD/ALS which provides evidence to link the pathology and genetics of these diseases. A large number of seemingly disparate physiological functions are damaged in FTD/ALS. However, many of these damaged functions are regulated by signalling between the endoplasmic reticulum and mitochondria, and this has stimulated investigations into the role of endoplasmic reticulum-mitochondria signalling in FTD/ALS disease processes. Here, we review progress on this topic.
format Online
Article
Text
id pubmed-5832427
institution National Center for Biotechnology Information
language English
publishDate 2018
publisher Nature Publishing Group UK
record_format MEDLINE/PubMed
spelling pubmed-58324272018-03-05 Disruption of ER−mitochondria signalling in fronto-temporal dementia and related amyotrophic lateral sclerosis Lau, Dawn H. W. Hartopp, Naomi Welsh, Natalie J. Mueller, Sarah Glennon, Elizabeth B. Mórotz, Gábor M. Annibali, Ambra Gomez-Suaga, Patricia Stoica, Radu Paillusson, Sebastien Miller, Christopher C. J. Cell Death Dis Review Article Fronto-temporal dementia (FTD) and amyotrophic lateral sclerosis (ALS) are two related and incurable neurodegenerative diseases. Features of these diseases include pathological protein inclusions in affected neurons with TAR DNA-binding protein 43 (TDP-43), dipeptide repeat proteins derived from the C9ORF72 gene, and fused in sarcoma (FUS) representing major constituent proteins in these inclusions. Mutations in C9ORF72 and the genes encoding TDP-43 and FUS cause familial forms of FTD/ALS which provides evidence to link the pathology and genetics of these diseases. A large number of seemingly disparate physiological functions are damaged in FTD/ALS. However, many of these damaged functions are regulated by signalling between the endoplasmic reticulum and mitochondria, and this has stimulated investigations into the role of endoplasmic reticulum-mitochondria signalling in FTD/ALS disease processes. Here, we review progress on this topic. Nature Publishing Group UK 2018-02-28 /pmc/articles/PMC5832427/ /pubmed/29491392 http://dx.doi.org/10.1038/s41419-017-0022-7 Text en © The Author(s) 2018 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/.
spellingShingle Review Article
Lau, Dawn H. W.
Hartopp, Naomi
Welsh, Natalie J.
Mueller, Sarah
Glennon, Elizabeth B.
Mórotz, Gábor M.
Annibali, Ambra
Gomez-Suaga, Patricia
Stoica, Radu
Paillusson, Sebastien
Miller, Christopher C. J.
Disruption of ER−mitochondria signalling in fronto-temporal dementia and related amyotrophic lateral sclerosis
title Disruption of ER−mitochondria signalling in fronto-temporal dementia and related amyotrophic lateral sclerosis
title_full Disruption of ER−mitochondria signalling in fronto-temporal dementia and related amyotrophic lateral sclerosis
title_fullStr Disruption of ER−mitochondria signalling in fronto-temporal dementia and related amyotrophic lateral sclerosis
title_full_unstemmed Disruption of ER−mitochondria signalling in fronto-temporal dementia and related amyotrophic lateral sclerosis
title_short Disruption of ER−mitochondria signalling in fronto-temporal dementia and related amyotrophic lateral sclerosis
title_sort disruption of er−mitochondria signalling in fronto-temporal dementia and related amyotrophic lateral sclerosis
topic Review Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5832427/
https://www.ncbi.nlm.nih.gov/pubmed/29491392
http://dx.doi.org/10.1038/s41419-017-0022-7
work_keys_str_mv AT laudawnhw disruptionofermitochondriasignallinginfrontotemporaldementiaandrelatedamyotrophiclateralsclerosis
AT hartoppnaomi disruptionofermitochondriasignallinginfrontotemporaldementiaandrelatedamyotrophiclateralsclerosis
AT welshnataliej disruptionofermitochondriasignallinginfrontotemporaldementiaandrelatedamyotrophiclateralsclerosis
AT muellersarah disruptionofermitochondriasignallinginfrontotemporaldementiaandrelatedamyotrophiclateralsclerosis
AT glennonelizabethb disruptionofermitochondriasignallinginfrontotemporaldementiaandrelatedamyotrophiclateralsclerosis
AT morotzgaborm disruptionofermitochondriasignallinginfrontotemporaldementiaandrelatedamyotrophiclateralsclerosis
AT annibaliambra disruptionofermitochondriasignallinginfrontotemporaldementiaandrelatedamyotrophiclateralsclerosis
AT gomezsuagapatricia disruptionofermitochondriasignallinginfrontotemporaldementiaandrelatedamyotrophiclateralsclerosis
AT stoicaradu disruptionofermitochondriasignallinginfrontotemporaldementiaandrelatedamyotrophiclateralsclerosis
AT paillussonsebastien disruptionofermitochondriasignallinginfrontotemporaldementiaandrelatedamyotrophiclateralsclerosis
AT millerchristophercj disruptionofermitochondriasignallinginfrontotemporaldementiaandrelatedamyotrophiclateralsclerosis