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Mouse and Human Tau Expression in Different Brain Areas

BACKGROUND: An increase in tau protein is believed to be necessary for tau aggregation. However, whether this is due to increased expression of the endogenous tau promoter or protein accumulation due to proteostasis failure remains uncertain. OBJECTIVE: To analyze the expression of GFP protein under...

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Autores principales: Vallés-Saiz, Laura, Ruiz-Gabarre, Daniel, García-Escudero, Vega, Perry, George, Avila, Jesús, Hernández, Félix
Formato: Online Artículo Texto
Lenguaje:English
Publicado: IOS Press 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9696674/
https://www.ncbi.nlm.nih.gov/pubmed/36506485
http://dx.doi.org/10.3233/ADR-220051
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author Vallés-Saiz, Laura
Ruiz-Gabarre, Daniel
García-Escudero, Vega
Perry, George
Avila, Jesús
Hernández, Félix
author_facet Vallés-Saiz, Laura
Ruiz-Gabarre, Daniel
García-Escudero, Vega
Perry, George
Avila, Jesús
Hernández, Félix
author_sort Vallés-Saiz, Laura
collection PubMed
description BACKGROUND: An increase in tau protein is believed to be necessary for tau aggregation. However, whether this is due to increased expression of the endogenous tau promoter or protein accumulation due to proteostasis failure remains uncertain. OBJECTIVE: To analyze the expression of GFP protein under endogenous tau promoter across different ages and within different brain areas. METHODS: We have measured direct expression of Mapt gene promotor by western blot and immunofluorescence, by means of a commercial tau knock-out mice generated by integrating GFP-encoding cDNA into exon 1 of the Mapt gene. Besides, we have analyzed the MAPT gene expression in human samples. RESULTS: Mapt expression is similar in the cortex, hippocampus, and cerebellum in mice and in human samples although some differences exist between dentate gyrus and CA1 hippocampal areas in mice. Besides, we have analyzed the murine Mapt gene expression during aging (at 2, 6, 12, and 18 moths) and no differences in endogenous tau promoter expression were observed. CONCLUSION: Our results suggest that Mapt promoter activity is similar in the brain areas studied and, therefore, tau accumulation due to aging is likely due to proteostasis failure rather than occurring at the transcriptional level.
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spelling pubmed-96966742022-12-08 Mouse and Human Tau Expression in Different Brain Areas Vallés-Saiz, Laura Ruiz-Gabarre, Daniel García-Escudero, Vega Perry, George Avila, Jesús Hernández, Félix J Alzheimers Dis Rep Research Report BACKGROUND: An increase in tau protein is believed to be necessary for tau aggregation. However, whether this is due to increased expression of the endogenous tau promoter or protein accumulation due to proteostasis failure remains uncertain. OBJECTIVE: To analyze the expression of GFP protein under endogenous tau promoter across different ages and within different brain areas. METHODS: We have measured direct expression of Mapt gene promotor by western blot and immunofluorescence, by means of a commercial tau knock-out mice generated by integrating GFP-encoding cDNA into exon 1 of the Mapt gene. Besides, we have analyzed the MAPT gene expression in human samples. RESULTS: Mapt expression is similar in the cortex, hippocampus, and cerebellum in mice and in human samples although some differences exist between dentate gyrus and CA1 hippocampal areas in mice. Besides, we have analyzed the murine Mapt gene expression during aging (at 2, 6, 12, and 18 moths) and no differences in endogenous tau promoter expression were observed. CONCLUSION: Our results suggest that Mapt promoter activity is similar in the brain areas studied and, therefore, tau accumulation due to aging is likely due to proteostasis failure rather than occurring at the transcriptional level. IOS Press 2022-11-03 /pmc/articles/PMC9696674/ /pubmed/36506485 http://dx.doi.org/10.3233/ADR-220051 Text en © 2022 – The authors. Published by IOS Press https://creativecommons.org/licenses/by-nc/4.0/This is an open access article distributed under the terms of the Creative Commons Attribution Non-Commercial (CC BY-NC 4.0) License (https://creativecommons.org/licenses/by-nc/4.0/) , which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Report
Vallés-Saiz, Laura
Ruiz-Gabarre, Daniel
García-Escudero, Vega
Perry, George
Avila, Jesús
Hernández, Félix
Mouse and Human Tau Expression in Different Brain Areas
title Mouse and Human Tau Expression in Different Brain Areas
title_full Mouse and Human Tau Expression in Different Brain Areas
title_fullStr Mouse and Human Tau Expression in Different Brain Areas
title_full_unstemmed Mouse and Human Tau Expression in Different Brain Areas
title_short Mouse and Human Tau Expression in Different Brain Areas
title_sort mouse and human tau expression in different brain areas
topic Research Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9696674/
https://www.ncbi.nlm.nih.gov/pubmed/36506485
http://dx.doi.org/10.3233/ADR-220051
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