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De novo actin polymerization is required for model Hirano body formation in Dictyostelium
Hirano bodies are eosinophilic, actin-rich inclusions found in autopsied brains in numerous neurodegenerative diseases. The mechanism of Hirano body formation is unknown. Mass spectrometry analysis was performed to identify proteins from partially purified model Hirano bodies from Dictyostelium. Thi...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Company of Biologists Ltd
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4920178/ https://www.ncbi.nlm.nih.gov/pubmed/27215322 http://dx.doi.org/10.1242/bio.014944 |
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author | Dong, Yun Shahid-Salles, Sonbol Sherling, Dan Fechheimer, Nathan Iyer, Nathan Wells, Lance Fechheimer, Marcus Furukawa, Ruth |
author_facet | Dong, Yun Shahid-Salles, Sonbol Sherling, Dan Fechheimer, Nathan Iyer, Nathan Wells, Lance Fechheimer, Marcus Furukawa, Ruth |
author_sort | Dong, Yun |
collection | PubMed |
description | Hirano bodies are eosinophilic, actin-rich inclusions found in autopsied brains in numerous neurodegenerative diseases. The mechanism of Hirano body formation is unknown. Mass spectrometry analysis was performed to identify proteins from partially purified model Hirano bodies from Dictyostelium. This analysis identified proteins primarily belonging to ribosomes, proteasomes, mitochondria and cytoskeleton. Profilin, Arp/2/3 and WASH identified by mass spectrometry were found to colocalise with model Hirano bodies. Due to their roles in actin regulation, we selected these proteins for further investigation. Inhibition of the Arp2/3 complex by CK666 prevented formation of model Hirano bodies. Since Arp2/3 activation occurs via the WASH or WAVE complex, we next investigated how these proteins affect Hirano body formation. Whereas model Hirano bodies could form in WASH-deficient cells, they failed to form in cells lacking HSPC300, a member of the WAVE complex. We identified other proteins required for Hirano body formation that include profilin and VASP, an actin nucleation factor. In the case of VASP, both its G- and F-actin binding domains were required for model Hirano body formation. Collectively, our results indicate that de novo actin polymerization is required to form model Hirano bodies. |
format | Online Article Text |
id | pubmed-4920178 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | The Company of Biologists Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-49201782016-07-07 De novo actin polymerization is required for model Hirano body formation in Dictyostelium Dong, Yun Shahid-Salles, Sonbol Sherling, Dan Fechheimer, Nathan Iyer, Nathan Wells, Lance Fechheimer, Marcus Furukawa, Ruth Biol Open Research Article Hirano bodies are eosinophilic, actin-rich inclusions found in autopsied brains in numerous neurodegenerative diseases. The mechanism of Hirano body formation is unknown. Mass spectrometry analysis was performed to identify proteins from partially purified model Hirano bodies from Dictyostelium. This analysis identified proteins primarily belonging to ribosomes, proteasomes, mitochondria and cytoskeleton. Profilin, Arp/2/3 and WASH identified by mass spectrometry were found to colocalise with model Hirano bodies. Due to their roles in actin regulation, we selected these proteins for further investigation. Inhibition of the Arp2/3 complex by CK666 prevented formation of model Hirano bodies. Since Arp2/3 activation occurs via the WASH or WAVE complex, we next investigated how these proteins affect Hirano body formation. Whereas model Hirano bodies could form in WASH-deficient cells, they failed to form in cells lacking HSPC300, a member of the WAVE complex. We identified other proteins required for Hirano body formation that include profilin and VASP, an actin nucleation factor. In the case of VASP, both its G- and F-actin binding domains were required for model Hirano body formation. Collectively, our results indicate that de novo actin polymerization is required to form model Hirano bodies. The Company of Biologists Ltd 2016-05-23 /pmc/articles/PMC4920178/ /pubmed/27215322 http://dx.doi.org/10.1242/bio.014944 Text en © 2016. Published by The Company of Biologists Ltd http://creativecommons.org/licenses/by/3.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/3.0), which permits unrestricted use, distribution and reproduction in any medium provided that the original work is properly attributed. |
spellingShingle | Research Article Dong, Yun Shahid-Salles, Sonbol Sherling, Dan Fechheimer, Nathan Iyer, Nathan Wells, Lance Fechheimer, Marcus Furukawa, Ruth De novo actin polymerization is required for model Hirano body formation in Dictyostelium |
title | De novo actin polymerization is required for model Hirano body formation in Dictyostelium |
title_full | De novo actin polymerization is required for model Hirano body formation in Dictyostelium |
title_fullStr | De novo actin polymerization is required for model Hirano body formation in Dictyostelium |
title_full_unstemmed | De novo actin polymerization is required for model Hirano body formation in Dictyostelium |
title_short | De novo actin polymerization is required for model Hirano body formation in Dictyostelium |
title_sort | de novo actin polymerization is required for model hirano body formation in dictyostelium |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4920178/ https://www.ncbi.nlm.nih.gov/pubmed/27215322 http://dx.doi.org/10.1242/bio.014944 |
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