Tau causes synapse loss without disrupting calcium homeostasis in the rTg4510 model of tauopathy.

Neurofibrillary tangles (NFTs) of tau are one of the defining hallmarks of Alzheimer's disease (AD), and are closely associated with neuronal degeneration. Although it has been suggested that calcium dysregulation is important to AD pathogenesis, few studies have probed the link between calcium...

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Autores principales: Katherine J Kopeikina, Susanne Wegmann, Rose Pitstick, George A Carlson, Brian J Bacskai, Rebecca A Betensky, Bradley T Hyman, Tara L Spires-Jones
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Publicado: Public Library of Science (PLoS) 2013
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Acceso en línea:https://doaj.org/article/020431432a1f4c968396a817fd88776f
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spelling oai:doaj.org-article:020431432a1f4c968396a817fd88776f2021-11-18T08:45:25ZTau causes synapse loss without disrupting calcium homeostasis in the rTg4510 model of tauopathy.1932-620310.1371/journal.pone.0080834https://doaj.org/article/020431432a1f4c968396a817fd88776f2013-01-01T00:00:00Zhttps://www.ncbi.nlm.nih.gov/pmc/articles/pmid/24278327/pdf/?tool=EBIhttps://doaj.org/toc/1932-6203Neurofibrillary tangles (NFTs) of tau are one of the defining hallmarks of Alzheimer's disease (AD), and are closely associated with neuronal degeneration. Although it has been suggested that calcium dysregulation is important to AD pathogenesis, few studies have probed the link between calcium homeostasis, synapse loss and pathological changes in tau. Here we test the hypothesis that pathological changes in tau are associated with changes in calcium by utilizing in vivo calcium imaging in adult rTg4510 mice that exhibit severe tau pathology due to over-expression of human mutant P301L tau. We observe prominent dendritic spine loss without disruptions in calcium homeostasis, indicating that tangles do not disrupt this fundamental feature of neuronal health, and that tau likely induces spine loss in a calcium-independent manner.Katherine J KopeikinaSusanne WegmannRose PitstickGeorge A CarlsonBrian J BacskaiRebecca A BetenskyBradley T HymanTara L Spires-JonesPublic Library of Science (PLoS)articleMedicineRScienceQENPLoS ONE, Vol 8, Iss 11, p e80834 (2013)
institution DOAJ
collection DOAJ
language EN
topic Medicine
R
Science
Q
spellingShingle Medicine
R
Science
Q
Katherine J Kopeikina
Susanne Wegmann
Rose Pitstick
George A Carlson
Brian J Bacskai
Rebecca A Betensky
Bradley T Hyman
Tara L Spires-Jones
Tau causes synapse loss without disrupting calcium homeostasis in the rTg4510 model of tauopathy.
description Neurofibrillary tangles (NFTs) of tau are one of the defining hallmarks of Alzheimer's disease (AD), and are closely associated with neuronal degeneration. Although it has been suggested that calcium dysregulation is important to AD pathogenesis, few studies have probed the link between calcium homeostasis, synapse loss and pathological changes in tau. Here we test the hypothesis that pathological changes in tau are associated with changes in calcium by utilizing in vivo calcium imaging in adult rTg4510 mice that exhibit severe tau pathology due to over-expression of human mutant P301L tau. We observe prominent dendritic spine loss without disruptions in calcium homeostasis, indicating that tangles do not disrupt this fundamental feature of neuronal health, and that tau likely induces spine loss in a calcium-independent manner.
format article
author Katherine J Kopeikina
Susanne Wegmann
Rose Pitstick
George A Carlson
Brian J Bacskai
Rebecca A Betensky
Bradley T Hyman
Tara L Spires-Jones
author_facet Katherine J Kopeikina
Susanne Wegmann
Rose Pitstick
George A Carlson
Brian J Bacskai
Rebecca A Betensky
Bradley T Hyman
Tara L Spires-Jones
author_sort Katherine J Kopeikina
title Tau causes synapse loss without disrupting calcium homeostasis in the rTg4510 model of tauopathy.
title_short Tau causes synapse loss without disrupting calcium homeostasis in the rTg4510 model of tauopathy.
title_full Tau causes synapse loss without disrupting calcium homeostasis in the rTg4510 model of tauopathy.
title_fullStr Tau causes synapse loss without disrupting calcium homeostasis in the rTg4510 model of tauopathy.
title_full_unstemmed Tau causes synapse loss without disrupting calcium homeostasis in the rTg4510 model of tauopathy.
title_sort tau causes synapse loss without disrupting calcium homeostasis in the rtg4510 model of tauopathy.
publisher Public Library of Science (PLoS)
publishDate 2013
url https://doaj.org/article/020431432a1f4c968396a817fd88776f
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