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Campo DCValorIdioma
dc.creatorEira, J
dc.creatorMagalhães, J
dc.creatorMacedo, N
dc.creatorPero, ME
dc.creatorMisgeld, T
dc.creatorSousa, MM
dc.creatorBartolini, F
dc.creatorLiz, MA
dc.date.accessioned2023-12-11T15:45:37Z-
dc.date.available2023-12-11T15:45:37Z-
dc.date.issued2021
dc.identifier.issn2296-634X
dc.identifier.urihttps://hdl.handle.net/10216/155606-
dc.description.abstractTransthyretin (TTR), a plasma and cerebrospinal fluid protein, increases axon growth and organelle transport in sensory neurons. While neurons extend their axons, the microtubule (MT) cytoskeleton is crucial for the segregation of functional compartments and axonal outgrowth. Herein, we investigated whether TTR promotes axon elongation by modulating MT dynamics. We found that TTR KO mice have an intrinsic increase in dynamic MTs and reduced levels of acetylated a-tubulin in peripheral axons. In addition, they failed to modulate MT dynamics in response to sciatic nerve injury, leading to decreased regenerative capacity. Importantly, restoring acetylated a-tubulin levels of TTR KO dorsal root ganglia (DRG) neurons using an HDAC6 inhibitor is sufficient to completely revert defective MT dynamics and neurite outgrowth. In summary, our results reveal a new role for TTR in the modulation of MT dynamics by regulating a-tubulin acetylation via modulation of the acetylase ATAT1, and suggest that this activity underlies TTR neuritogenic function.
dc.description.sponsorshipThis work was supported by: FEDER – Fundo Europeu de Desenvolvimento Regional funds through the COMPETE 2020 – Operacional Programme for Competitiveness and Internationalisation (POCI), Portugal 2020, and by Portuguese funds through FCT – Fundação para a Ciência e a Tecnologia/Ministério da Ciéncia, Tecnologia e Ensino Superior in the framework of the project POCI-01-0145-FEDER-028336 (PTDC/MED-NEU/28336/2017); Norte-01-0145-FEDER-000008 – Porto Neurosciences and Neurologic Disease Research Initiative at I3S, supported by Norte Portugal Regional Operational Programme (NORTE 2020), under the PORTUGAL 2020 Partnership Agreement, through FEDER; and Thompson Family Foundation (TFFI) award, RO1AG050658 (NIH/National Institute on Aging) and R21NS120076 (NIH/NINDS) awards to FB, and a PRIN-2017FJC3-004 (MIUR) to MEP. TM is supported by the Deutsche Forshcunggemeinschaft (EXC 2145 SyNergy – ID 390857198; TRR 274/1 2020 – ID 408885537). JE is a FCT fellow (SFRH/BD/116343/2016). MAL is an FCT Investigator (IF/00902/2015).
dc.language.isoeng
dc.publisher Frontiers Media
dc.relation.ispartofFrontiers in Cell and Developmental Biology, vol.9:747699
dc.rightsopenAccess
dc.rights.urihttps://creativecommons.org/licenses/by/4.0/
dc.subjectAxon growth
dc.subjectMicrotubules
dc.subjectNerve biology
dc.subjectTransthyretin
dc.subjectTransthyretin amyloid polyneuropathy
dc.subjectTubulin acetylation
dc.titleTransthyretin Promotes Axon Growth via Regulation of Microtubule Dynamics and Tubulin Acetylation
dc.typeArtigo em Revista Científica Internacional
dc.contributor.uportoInstituto de Investigação e Inovação em Saúde
dc.identifier.doi10.3389/fcell.2021.747699
dc.relation.publisherversionhttps://www.frontiersin.org/articles/10.3389/fcell.2021.747699/full
Aparece nas coleções:I3S - Artigo em Revista Científica Internacional

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