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PTEN activation contributes to neuronal and synaptic engulfment by microglia in tauopathy
Phosphatase and tensin homolog (PTEN) regulates synaptic density in development; however, whether PTEN also regulates synapse loss in a neurodegenerative disorder such as frontotemporal lobar degeneration with Tau deposition (FTLD-Tau) has not been explored. Here, we found that pathological Tau prom...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Springer Berlin Heidelberg
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7300099/ https://www.ncbi.nlm.nih.gov/pubmed/32236736 http://dx.doi.org/10.1007/s00401-020-02151-9 |
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author | Benetatos, Joseph Bennett, Rachel E. Evans, Harrison T. Ellis, Sevannah A. Hyman, Bradley T. Bodea, Liviu-Gabriel Götz, Jürgen |
author_facet | Benetatos, Joseph Bennett, Rachel E. Evans, Harrison T. Ellis, Sevannah A. Hyman, Bradley T. Bodea, Liviu-Gabriel Götz, Jürgen |
author_sort | Benetatos, Joseph |
collection | PubMed |
description | Phosphatase and tensin homolog (PTEN) regulates synaptic density in development; however, whether PTEN also regulates synapse loss in a neurodegenerative disorder such as frontotemporal lobar degeneration with Tau deposition (FTLD-Tau) has not been explored. Here, we found that pathological Tau promotes early activation of PTEN, which precedes apoptotic caspase-3 cleavage in the rTg4510 mouse model of FTLD-Tau. We further demonstrate increased synaptic and neuronal exposure of the apoptotic signal phosphatidylserine that tags neuronal structures for microglial uptake, thereby linking PTEN activation to synaptic and neuronal structure elimination. By applying pharmacological inhibition of PTEN's protein phosphatase activity, we observed that microglial uptake can be decreased in Tau transgenic mice. Finally, we reveal a dichotomous relationship between PTEN activation and age in FTLD-Tau patients and healthy controls. Together, our findings suggest that in tauopathy, PTEN has a role in the synaptotoxicity of pathological Tau and promotes microglial removal of affected neuronal structures. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1007/s00401-020-02151-9) contains supplementary material, which is available to authorized users. |
format | Online Article Text |
id | pubmed-7300099 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Springer Berlin Heidelberg |
record_format | MEDLINE/PubMed |
spelling | pubmed-73000992020-06-22 PTEN activation contributes to neuronal and synaptic engulfment by microglia in tauopathy Benetatos, Joseph Bennett, Rachel E. Evans, Harrison T. Ellis, Sevannah A. Hyman, Bradley T. Bodea, Liviu-Gabriel Götz, Jürgen Acta Neuropathol Original Paper Phosphatase and tensin homolog (PTEN) regulates synaptic density in development; however, whether PTEN also regulates synapse loss in a neurodegenerative disorder such as frontotemporal lobar degeneration with Tau deposition (FTLD-Tau) has not been explored. Here, we found that pathological Tau promotes early activation of PTEN, which precedes apoptotic caspase-3 cleavage in the rTg4510 mouse model of FTLD-Tau. We further demonstrate increased synaptic and neuronal exposure of the apoptotic signal phosphatidylserine that tags neuronal structures for microglial uptake, thereby linking PTEN activation to synaptic and neuronal structure elimination. By applying pharmacological inhibition of PTEN's protein phosphatase activity, we observed that microglial uptake can be decreased in Tau transgenic mice. Finally, we reveal a dichotomous relationship between PTEN activation and age in FTLD-Tau patients and healthy controls. Together, our findings suggest that in tauopathy, PTEN has a role in the synaptotoxicity of pathological Tau and promotes microglial removal of affected neuronal structures. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1007/s00401-020-02151-9) contains supplementary material, which is available to authorized users. Springer Berlin Heidelberg 2020-03-31 2020 /pmc/articles/PMC7300099/ /pubmed/32236736 http://dx.doi.org/10.1007/s00401-020-02151-9 Text en © The Author(s) 2020 Open AccessThis 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 licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence 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 licence, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Original Paper Benetatos, Joseph Bennett, Rachel E. Evans, Harrison T. Ellis, Sevannah A. Hyman, Bradley T. Bodea, Liviu-Gabriel Götz, Jürgen PTEN activation contributes to neuronal and synaptic engulfment by microglia in tauopathy |
title | PTEN activation contributes to neuronal and synaptic engulfment by microglia in tauopathy |
title_full | PTEN activation contributes to neuronal and synaptic engulfment by microglia in tauopathy |
title_fullStr | PTEN activation contributes to neuronal and synaptic engulfment by microglia in tauopathy |
title_full_unstemmed | PTEN activation contributes to neuronal and synaptic engulfment by microglia in tauopathy |
title_short | PTEN activation contributes to neuronal and synaptic engulfment by microglia in tauopathy |
title_sort | pten activation contributes to neuronal and synaptic engulfment by microglia in tauopathy |
topic | Original Paper |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7300099/ https://www.ncbi.nlm.nih.gov/pubmed/32236736 http://dx.doi.org/10.1007/s00401-020-02151-9 |
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