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    <identifier identifierType="DOI">10.34691/UCHILE/4MDLCP</identifier>
    <creators><creator><creatorName>Hetz, Claudio</creatorName><nameIdentifier schemeURI="https://orcid.org/" nameIdentifierScheme="ORCID">0000-0003-1120-7966</nameIdentifier><affiliation>(Universidad de Chile - Facultad de Medicina)</affiliation></creator><creator><creatorName>Vicente Valenzuela</creatorName><affiliation>(Biomedical Neuroscience, Faculty of Medicine, Universidad de Chile, Santiago, Chile)</affiliation></creator><creator><creatorName>Daniela Becerra</creatorName></creator><creator><creatorName>José Astorga</creatorName></creator><creator><creatorName>Matias Fuentealba</creatorName></creator><creator><creatorName>Guillermo Diaz</creatorName></creator><creator><creatorName>Leslie Bargsted</creatorName></creator><creator><creatorName>Carlos Chacón</creatorName></creator><creator><creatorName>Alexis Martinez</creatorName></creator><creator><creatorName>Romina Gozalvo</creatorName></creator><creator><creatorName>Kasey Jackson</creatorName><affiliation>(Sanofi Genzyme Corp., Cambridge Ma, USA)</affiliation></creator><creator><creatorName>Vania Morales</creatorName></creator><creator><creatorName>Macarena Las Heras</creatorName></creator><creator><creatorName>Giovanni Tamburini</creatorName></creator><creator><creatorName>Leonard Petrucelli</creatorName></creator><creator><creatorName>Pablo Sardi</creatorName></creator><creator><creatorName>Lars Plate</creatorName></creator></creators>
    <titles>
        <title>Artificial enforcement of the unfolded protein response (UPR) reduces disease features in multiple preclinical models of ALS/FTD.</title>
    </titles>
    <publisher>Repositorio de datos de investigación de la Universidad de Chile</publisher>
    <publicationYear>2024</publicationYear>
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    <relatedIdentifiers><relatedIdentifier relatedIdentifierType="DOI" relationType="HasPart">doi:10.34691/UCHILE/4MDLCP/K2H1P4</relatedIdentifier></relatedIdentifiers>
    <descriptions>
        <description descriptionType="Abstract">Data used for Research Article submission to Molecular Therapy Journal for review Amyotrophic lateral sclerosis (ALS) and fronto-temporal dementia (FTD) are part of a spectrum of diseases that share several causative genes, resulting on a combinatory of motor and cognitive symptoms and abnormal protein aggregation. Multiple unbiased studies have revealed that proteostasis impairment at the level of the endoplasmic reticulum (ER) is a transversal pathogenic feature of ALS/FTD. The transcription factor XBP1s is a master regulator of the unfolded protein response (UPR), the main adaptive pathway to cope with ER stress. Here we provide evidence of suboptimal activation of the UPR in ALS/FTD models under experimental ER stress. To artificially engage the UPR, we intracerebroventricularly administrated adeno-associated viruses (AAV) to express the active form of XBP1 (XBP1s) in the nervous system of ALS/FTD models. XBP1s expression improved motor performance and extended life span of mutant SOD1 mice, associated with reduced protein aggregation. AAV-XBP1s administration also attenuated disease progression in models of TDP-43 and C9orf72 pathogenesis. Proteomic profiling of spinal cord tissue revealed that XBP1s overexpression improved proteostasis and modulated the expression of a cluster of synaptic and cell morphology proteins. Our results suggest that strategies to improve ER proteostasis may serve as a pan-therapeutic strategy to treat ALS/FTD.</description>
    </descriptions>
    <contributors><contributor contributorType="ContactPerson"><contributorName>Hetz, Claudio</contributorName><affiliation>(Universidad de Chile - Facultad de Medicina)</affiliation></contributor></contributors>
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