Selective impact of Tau loss on nociceptive primary afferents and pain sensation

Detalhes bibliográficos
Autor(a) principal: Sotiropoulos, I.
Data de Publicação: 2014
Outros Autores: Lopes, André T., Pinto, Vítor, Lopes, Sofia, Carlos, Sara, Silva, Sara Carina Duarte, Carvalho, Andreia Alexandra Neves de, Ribeiro, Filipa Pinto, Pinheiro, Sara, Fernandes, Rui, Almeida, Armando, Sousa, Nuno, Almeida, Hugo Leite
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)
Texto Completo: http://hdl.handle.net/1822/33065
Resumo: Tau protein hyperphosphorylation and consequent malfunction are hallmarks of Alzheimer's disease pathology; importantly, pain perception is diminished in these patients. In physiological conditions, Tau contributes to cytoskeletal dynamics and in this way, influences a number of cellular mechanisms including axonal trafficking, myelination and synaptic plasticity, processes that are also implicated in pain perception. However, there is no in vivo evidence clarifying the role of Tau in nociception. Thus, we tested Tau-null (Tau-/-) and Tau+/+ mice for acute thermal pain (Hargreaves' test), acute and tonic inflammatory pain (formalin test) and mechanical allodynia (Von Frey test). We report that Tau-/- animals presented a decreased response to acute noxious stimuli when compared to Tau+/+ while their pain-related behavior is augmented under tonic painful stimuli. This increased reactivity to tonic pain was accompanied by enhanced formalin-evoked c-fos staining of second order nociceptive neurons at Tau-null dorsal horn. In addition, we analyzed the primary afferents conveying nociceptive signals, estimating sciatic nerve fiber density, myelination and nerve conduction. Ultrastructural analysis revealed a decreased C-fiber density in the sciatic nerve of Tau-null mice and a hypomyelination of myelinated fibers (Ad-fibers) - also confirmed by western blot analysis - followed by altered conduction properties of Tau-null sciatic nerves. To our knowledge, this is the first in vivo study that demonstrates that Tau depletion negatively affects the main systems conveying nociceptive information to the CNS, adding to our knowledge about Tau function(s) that might also be relevant for understanding peripheral neurological deficits in different Tauopathies.
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spelling Selective impact of Tau loss on nociceptive primary afferents and pain sensationTauPainPeripheral nerveMyelinationC-fibersScience & TechnologyTau protein hyperphosphorylation and consequent malfunction are hallmarks of Alzheimer's disease pathology; importantly, pain perception is diminished in these patients. In physiological conditions, Tau contributes to cytoskeletal dynamics and in this way, influences a number of cellular mechanisms including axonal trafficking, myelination and synaptic plasticity, processes that are also implicated in pain perception. However, there is no in vivo evidence clarifying the role of Tau in nociception. Thus, we tested Tau-null (Tau-/-) and Tau+/+ mice for acute thermal pain (Hargreaves' test), acute and tonic inflammatory pain (formalin test) and mechanical allodynia (Von Frey test). We report that Tau-/- animals presented a decreased response to acute noxious stimuli when compared to Tau+/+ while their pain-related behavior is augmented under tonic painful stimuli. This increased reactivity to tonic pain was accompanied by enhanced formalin-evoked c-fos staining of second order nociceptive neurons at Tau-null dorsal horn. In addition, we analyzed the primary afferents conveying nociceptive signals, estimating sciatic nerve fiber density, myelination and nerve conduction. Ultrastructural analysis revealed a decreased C-fiber density in the sciatic nerve of Tau-null mice and a hypomyelination of myelinated fibers (Ad-fibers) - also confirmed by western blot analysis - followed by altered conduction properties of Tau-null sciatic nerves. To our knowledge, this is the first in vivo study that demonstrates that Tau depletion negatively affects the main systems conveying nociceptive information to the CNS, adding to our knowledge about Tau function(s) that might also be relevant for understanding peripheral neurological deficits in different Tauopathies.We would like to thank Drs Joao Relvas, Joana Paes de Faria Monteiro and Nuno Dias for their comments in this work. Many thanks to Dr Joao Relvas for the MBP antibody. The work was supported by grants "SFRH/BPD/80118/2011", "PTDC/SAU-NMC/113934/2009" funded by FCT - Portuguese Foundation for Science and Technology and project DoIT - Desenvolvimento e Operacionalizacao da Investigacao de Translacao (No. do projeto 13853), funded by Fund Europeu de Desenvolvimento Regional (FEDER) through the Programa Operacional Fatores de Competitividade (POFC). Author's contributions: experimental design - IS, HA, VP, AA, and NS; performed research - IS, HA, VP, AL, SL, SS, SP, AC, FPR, and RF; data analyses - IS, HA, AL, VP, SC, and FPR; and manuscript preparation - IS, HA, VP, and NS.ElsevierUniversidade do MinhoSotiropoulos, I.Lopes, André T.Pinto, VítorLopes, SofiaCarlos, SaraSilva, Sara Carina DuarteCarvalho, Andreia Alexandra Neves deRibeiro, Filipa PintoPinheiro, SaraFernandes, RuiAlmeida, ArmandoSousa, NunoAlmeida, Hugo Leite2014-07-202014-07-20T00:00:00Zinfo:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/articleapplication/pdfhttp://hdl.handle.net/1822/33065eng0014-488610.1016/j.expneurol.2014.07.00825079367http://www.elsevier.com/info:eu-repo/semantics/openAccessreponame:Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)instname:Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informaçãoinstacron:RCAAP2024-05-11T04:22:23Zoai:repositorium.sdum.uminho.pt:1822/33065Portal AgregadorONGhttps://www.rcaap.pt/oai/openairemluisa.alvim@gmail.comopendoar:71602024-05-11T04:22:23Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) - Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informaçãofalse
dc.title.none.fl_str_mv Selective impact of Tau loss on nociceptive primary afferents and pain sensation
title Selective impact of Tau loss on nociceptive primary afferents and pain sensation
spellingShingle Selective impact of Tau loss on nociceptive primary afferents and pain sensation
Sotiropoulos, I.
Tau
Pain
Peripheral nerve
Myelination
C-fibers
Science & Technology
title_short Selective impact of Tau loss on nociceptive primary afferents and pain sensation
title_full Selective impact of Tau loss on nociceptive primary afferents and pain sensation
title_fullStr Selective impact of Tau loss on nociceptive primary afferents and pain sensation
title_full_unstemmed Selective impact of Tau loss on nociceptive primary afferents and pain sensation
title_sort Selective impact of Tau loss on nociceptive primary afferents and pain sensation
author Sotiropoulos, I.
author_facet Sotiropoulos, I.
Lopes, André T.
Pinto, Vítor
Lopes, Sofia
Carlos, Sara
Silva, Sara Carina Duarte
Carvalho, Andreia Alexandra Neves de
Ribeiro, Filipa Pinto
Pinheiro, Sara
Fernandes, Rui
Almeida, Armando
Sousa, Nuno
Almeida, Hugo Leite
author_role author
author2 Lopes, André T.
Pinto, Vítor
Lopes, Sofia
Carlos, Sara
Silva, Sara Carina Duarte
Carvalho, Andreia Alexandra Neves de
Ribeiro, Filipa Pinto
Pinheiro, Sara
Fernandes, Rui
Almeida, Armando
Sousa, Nuno
Almeida, Hugo Leite
author2_role author
author
author
author
author
author
author
author
author
author
author
author
dc.contributor.none.fl_str_mv Universidade do Minho
dc.contributor.author.fl_str_mv Sotiropoulos, I.
Lopes, André T.
Pinto, Vítor
Lopes, Sofia
Carlos, Sara
Silva, Sara Carina Duarte
Carvalho, Andreia Alexandra Neves de
Ribeiro, Filipa Pinto
Pinheiro, Sara
Fernandes, Rui
Almeida, Armando
Sousa, Nuno
Almeida, Hugo Leite
dc.subject.por.fl_str_mv Tau
Pain
Peripheral nerve
Myelination
C-fibers
Science & Technology
topic Tau
Pain
Peripheral nerve
Myelination
C-fibers
Science & Technology
description Tau protein hyperphosphorylation and consequent malfunction are hallmarks of Alzheimer's disease pathology; importantly, pain perception is diminished in these patients. In physiological conditions, Tau contributes to cytoskeletal dynamics and in this way, influences a number of cellular mechanisms including axonal trafficking, myelination and synaptic plasticity, processes that are also implicated in pain perception. However, there is no in vivo evidence clarifying the role of Tau in nociception. Thus, we tested Tau-null (Tau-/-) and Tau+/+ mice for acute thermal pain (Hargreaves' test), acute and tonic inflammatory pain (formalin test) and mechanical allodynia (Von Frey test). We report that Tau-/- animals presented a decreased response to acute noxious stimuli when compared to Tau+/+ while their pain-related behavior is augmented under tonic painful stimuli. This increased reactivity to tonic pain was accompanied by enhanced formalin-evoked c-fos staining of second order nociceptive neurons at Tau-null dorsal horn. In addition, we analyzed the primary afferents conveying nociceptive signals, estimating sciatic nerve fiber density, myelination and nerve conduction. Ultrastructural analysis revealed a decreased C-fiber density in the sciatic nerve of Tau-null mice and a hypomyelination of myelinated fibers (Ad-fibers) - also confirmed by western blot analysis - followed by altered conduction properties of Tau-null sciatic nerves. To our knowledge, this is the first in vivo study that demonstrates that Tau depletion negatively affects the main systems conveying nociceptive information to the CNS, adding to our knowledge about Tau function(s) that might also be relevant for understanding peripheral neurological deficits in different Tauopathies.
publishDate 2014
dc.date.none.fl_str_mv 2014-07-20
2014-07-20T00:00:00Z
dc.type.status.fl_str_mv info:eu-repo/semantics/publishedVersion
dc.type.driver.fl_str_mv info:eu-repo/semantics/article
format article
status_str publishedVersion
dc.identifier.uri.fl_str_mv http://hdl.handle.net/1822/33065
url http://hdl.handle.net/1822/33065
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv 0014-4886
10.1016/j.expneurol.2014.07.008
25079367
http://www.elsevier.com/
dc.rights.driver.fl_str_mv info:eu-repo/semantics/openAccess
eu_rights_str_mv openAccess
dc.format.none.fl_str_mv application/pdf
dc.publisher.none.fl_str_mv Elsevier
publisher.none.fl_str_mv Elsevier
dc.source.none.fl_str_mv reponame:Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)
instname:Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informação
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reponame_str Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)
collection Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)
repository.name.fl_str_mv Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) - Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informação
repository.mail.fl_str_mv mluisa.alvim@gmail.com
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