dc.creatorJuretić, Nevenka
dc.creatorDíaz, Josefina
dc.creatorRomero, Felipe
dc.creatorGonzález, Gustavo
dc.creatorJaimovich Pérez, Enrique
dc.creatorRiveros, Nora
dc.date.accessioned2019-03-18T11:55:31Z
dc.date.available2019-03-18T11:55:31Z
dc.date.created2019-03-18T11:55:31Z
dc.date.issued2017
dc.identifierBiochimica et Biophysica Acta - Molecular Basis of Disease, Volumen 1863, Issue 3, 2018, Pages 770-780
dc.identifier1879260X
dc.identifier09254439
dc.identifier10.1016/j.bbadis.2016.12.008
dc.identifierhttps://repositorio.uchile.cl/handle/2250/166977
dc.description.abstract© 2016 Elsevier B.V. Duchenne muscular dystrophy (DMD) is a neuromuscular disease originated by mutations in the dystrophin gene. A promising therapeutic approach deals with functional substitution of dystrophin by utrophin, a structural homolog that might be able to compensate dystrophin absence in DMD muscle fibers. It has been described that both interleukin-6 (IL-6) and neuregulin-1 (NRG-1; Heregulin-HRG) induce utrophin expression in skeletal muscle. We investigated a possible functional link among IL-6, NRG-1 and utrophin, in normal (C57) and dystrophic (mdx) skeletal muscle cells. Western Blot analysis allowed us to demonstrate that IL-6 (100 ng/mL) induces NRG-1 receptor phosphorylation (ErbB2/ErbB3) in both cell types, in a process that depends on intracellular Ca2 + and metalloproteinase activity; it also induces a transient increase of ERK1 and GABPα phosphorylation only in dystrophic myotubes. Semiquantitative PCR showed that IL-6 treatment increases utrophin mRNA levels ju
dc.languageen
dc.publisherElsevier B.V.
dc.rightshttp://creativecommons.org/licenses/by-nc-nd/3.0/cl/
dc.rightsAttribution-NonCommercial-NoDerivs 3.0 Chile
dc.sourceBiochimica et Biophysica Acta - Molecular Basis of Disease
dc.subjectDuchenne muscular dystrophy
dc.subjectDystrophin
dc.subjectMuscle gene expression
dc.subjectMyokine
dc.subjectNeuregulin
dc.subjectSkeletal muscle
dc.titleInterleukin-6 and neuregulin-1 as regulators of utrophin expression via the activation of NRG-1/ErbB signaling pathway in mdx cells
dc.typeArtículos de revistas


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