Articles producció científicaMedicina i Cirurgia

The BACE1 product sAPPβ induces ER stress and inflammation and impairs insulin signaling.

  • Datos identificativos

    Identificador:  imarina:5132425
    Autores:  Botteri, Gaia; Salvado, Laia; Guma, Anna; Hamilton, D Lee; Meakin, Paul J; Montagut, Gemma; Ashford, Michael L J; Ceperuelo-Mallafre, Victoria; Fernandez-Veledo, Sonia; Vendrell, Joan; Calderon-Dominguez, Maria; Serra, Dolors; Herrero, Laura; Pizarro, Javier; Barroso, Emma; Palomer, Xavier; Vazquez-Carrera, Manuel
    Resumen:
    ?-secretase/?-site amyloid precursor protein (APP)-cleaving enzyme 1 (BACE1) is a key enzyme involved in Alzheimer's disease that has recently been implicated in insulin-independent glucose uptake in myotubes. However, it is presently unknown whether BACE1 and the product of its activity, soluble APP? (sAPP?), contribute to lipid-induced inflammation and insulin resistance in skeletal muscle cells.Studies were conducted in mouse C2C12 myotubes, skeletal muscle from Bace1-/-mice and mice treated with sAPP? and adipose tissue and plasma from obese and type 2 diabetic patients.We show that BACE1 inhibition or knockdown attenuates palmitate-induced endoplasmic reticulum (ER) stress, inflammation, and insulin resistance and prevents the reduction in Peroxisome Proliferator-Activated Receptor ? Co-activator 1? (PGC-1?) and fatty acid oxidation caused by palmitate in myotubes. The effects of palmitate on ER stress, inflammation, insulin resistance, PGC-1? down-regulation, and fatty acid oxidation were mimicked by soluble APP? in vitro. BACE1 expression was increased in subcutaneous adipose tissue of obese and type 2 diabetic patients and this was accompanied by a decrease in PGC-1? mRNA levels and by an increase in sAPP? plasma levels of obese type 2 diabetic patients compared to obese non-diabetic subjects. Acute sAPP? administration to mice reduced PGC-1? levels and increased inflammation in skeletal muscle and decreased insulin sensitivity.Collectively, these findings indicate that the BACE1 product sAPP? is a key determinant in ER stress, inflammation and insulin resistance in skeletal muscle and gluconeogenesis in liver.Copyright © 2018 Elsevier Inc. All rights reserved.
  • Otros:

    Autor según el artículo: Botteri, Gaia; Salvado, Laia; Guma, Anna; Hamilton, D Lee; Meakin, Paul J; Montagut, Gemma; Ashford, Michael L J; Ceperuelo-Mallafre, Victoria; Fernandez-Veledo, Sonia; Vendrell, Joan; Calderon-Dominguez, Maria; Serra, Dolors; Herrero, Laura; Pizarro, Javier; Barroso, Emma; Palomer, Xavier; Vazquez-Carrera, Manuel
    Departamento: Bioquímica i Biotecnologia; Medicina i Cirurgia; Ciències Mèdiques Bàsiques
    Autor/es de la URV: Ceperuelo Mallafré, Maria Victoria / Fernandez Veledo, Sonia / Vendrell Ortega, Juan José
    Palabras clave: Skeletal-muscle; Signal transduction; Sappβ; Sapp?; Sapp beta; Resistance; Pgc-1α; Pgc-1?; Pgc-1-alpha; Pgc-1 alpha; Palmitic acid; Palmitate; Nf-κb; Nf-kappa b; Nf-?b; Muscle, skeletal; Muscle fibers, skeletal; Mitochondrial-function; Mice; Male; Insulin resistance; Insulin; Inflammation; Humans; Hepatic gluconeogenesis; Gene-transcription; Fatty-acids; Endoplasmic-reticulum stress; Endoplasmic reticulum stress; Creb; Cells, cultured; Cell line; Bace1 protein, mouse; Bace1; Aspartic acid endopeptidases; Animals; Amyloid-beta; Amyloid precursor protein secretases; Alpha gene; pgc-1?; palmitate; nf-?b; insulin resistance; creb; bace1
    Resumen: ?-secretase/?-site amyloid precursor protein (APP)-cleaving enzyme 1 (BACE1) is a key enzyme involved in Alzheimer's disease that has recently been implicated in insulin-independent glucose uptake in myotubes. However, it is presently unknown whether BACE1 and the product of its activity, soluble APP? (sAPP?), contribute to lipid-induced inflammation and insulin resistance in skeletal muscle cells.Studies were conducted in mouse C2C12 myotubes, skeletal muscle from Bace1-/-mice and mice treated with sAPP? and adipose tissue and plasma from obese and type 2 diabetic patients.We show that BACE1 inhibition or knockdown attenuates palmitate-induced endoplasmic reticulum (ER) stress, inflammation, and insulin resistance and prevents the reduction in Peroxisome Proliferator-Activated Receptor ? Co-activator 1? (PGC-1?) and fatty acid oxidation caused by palmitate in myotubes. The effects of palmitate on ER stress, inflammation, insulin resistance, PGC-1? down-regulation, and fatty acid oxidation were mimicked by soluble APP? in vitro. BACE1 expression was increased in subcutaneous adipose tissue of obese and type 2 diabetic patients and this was accompanied by a decrease in PGC-1? mRNA levels and by an increase in sAPP? plasma levels of obese type 2 diabetic patients compared to obese non-diabetic subjects. Acute sAPP? administration to mice reduced PGC-1? levels and increased inflammation in skeletal muscle and decreased insulin sensitivity.Collectively, these findings indicate that the BACE1 product sAPP? is a key determinant in ER stress, inflammation and insulin resistance in skeletal muscle and gluconeogenesis in liver.Copyright © 2018 Elsevier Inc. All rights reserved.
    Acceso a la licencia de uso: https://creativecommons.org/licenses/by/3.0/es/
    ISSN: 0026-0495
    Direcció de correo del autor: victoria.ceperuelo@urv.cat; sonia.fernandez@urv.cat; jvortega@iispv.cat
    Fecha de alta del registro: 2025-02-08
    Versión del articulo depositado: info:eu-repo/semantics/acceptedVersion
    Enlace a la fuente original: https://www.metabolismjournal.com/article/S0026-0495(18)30071-4/fulltext
    URL Documento de licencia: https://repositori.urv.cat/ca/proteccio-de-dades/
    Referencia al articulo segun fuente origial: Metabolism Clinical And Experimental. 85 59-75
    Referencia de l'ítem segons les normes APA: Botteri, Gaia; Salvado, Laia; Guma, Anna; Hamilton, D Lee; Meakin, Paul J; Montagut, Gemma; Ashford, Michael L J; Ceperuelo-Mallafre, Victoria; Fernan (2018). The BACE1 product sAPPβ induces ER stress and inflammation and impairs insulin signaling.. Metabolism Clinical And Experimental, 85(), 59-75. DOI: 10.1016/j.metabol.2018.03.005
    DOI del artículo: 10.1016/j.metabol.2018.03.005
    Entidad: Universitat Rovira i Virgili
    Año de publicación de la revista: 2018
    Tipo de publicación: Journal Publications
  • Palabras clave:

    Skeletal-muscle
    Signal transduction
    Sappβ
    Sapp?
    Sapp beta
    Resistance
    Pgc-1α
    Pgc-1?
    Pgc-1-alpha
    Pgc-1 alpha
    Palmitic acid
    Palmitate
    Nf-κb
    Nf-kappa b
    Nf-?b
    Muscle, skeletal
    Muscle fibers, skeletal
    Mitochondrial-function
    Mice
    Male
    Insulin resistance
    Insulin
    Inflammation
    Humans
    Hepatic gluconeogenesis
    Gene-transcription
    Fatty-acids
    Endoplasmic-reticulum stress
    Endoplasmic reticulum stress
    Creb
    Cells, cultured
    Cell line
    Bace1 protein, mouse
    Bace1
    Aspartic acid endopeptidases
    Animals
    Amyloid-beta
    Amyloid precursor protein secretases
    Alpha gene
    pgc-1?
    palmitate
    nf-?b
    insulin resistance
    creb
    bace1
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