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Chitinase 3-like 1 is neurotoxic in primary cultured neurons.
Matute-Blanch, Clara; Calvo-Barreiro, Laura; Carballo-Carbajal, Iria; Gonzalo, Ricardo; Sanchez, Alex; Vila, Miquel; Montalban, Xavier; Comabella, Manuel.
Afiliación
  • Matute-Blanch C; Servei de Neurologia-Neuroimmunologia, Centre d'Esclerosi Múltiple de Catalunya (Cemcat), Institut de Recerca Vall d'Hebron (VHIR), Hospital Universitari Vall d'Hebron, Universitat Autònoma de Barcelona, Barcelona, Spain. clara.matute@vhir.org.
  • Calvo-Barreiro L; Servei de Neurologia-Neuroimmunologia, Centre d'Esclerosi Múltiple de Catalunya (Cemcat), Institut de Recerca Vall d'Hebron (VHIR), Hospital Universitari Vall d'Hebron, Universitat Autònoma de Barcelona, Barcelona, Spain.
  • Carballo-Carbajal I; Neurodegenerative Diseases Research Group, Vall d'Hebron Research Institute-Center for Networked Biomedical Research on Neurodegenerative Diseases (CIBERNED), Barcelona, Spain.
  • Gonzalo R; Statistics and Bioinformatics Unit. Vall d'Hebron Institut de Recerca, Barcelona, Spain.
  • Sanchez A; Statistics and Bioinformatics Unit. Vall d'Hebron Institut de Recerca, Barcelona, Spain.
  • Vila M; Genetics, Microbiology and Statistics Department, Universitat de Barcelona, Barcelona, Spain.
  • Montalban X; Neurodegenerative Diseases Research Group, Vall d'Hebron Research Institute-Center for Networked Biomedical Research on Neurodegenerative Diseases (CIBERNED), Barcelona, Spain.
  • Comabella M; Department of Biochemistry and Molecular Biology, Autonomous University of Barcelona, Barcelona, Spain.
Sci Rep ; 10(1): 7118, 2020 04 28.
Article en En | MEDLINE | ID: mdl-32346016
ABSTRACT
Chitinase 3-like 1 (CHI3L1) is known to play a role as prognostic biomarker in the early stages of multiple sclerosis (MS), and patients with high cerebrospinal fluid CHI3L1 levels have an increased risk for the development of neurological disability. Here, we investigated its potential neurotoxic effect by adding recombinant CHI3L1 in vitro to primary cultures of mouse cortical neurons and evaluating both neuronal functionality and survival by immunofluorescence. CHI3L1 induced a significant neurite length retraction after 24 and 48 hours of exposure and significantly reduced neuronal survival at 48 hours. The cytotoxic effect of CHI3L1 was neuron-specific and was not observed in mouse immune or other central nervous system cells. These results point to a selective neurotoxic effect of CHI3L1 in vitro and suggest a potential role of CHI3L1 as therapeutic target in MS patients.
Asunto(s)

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Proteína 1 Similar a Quitinasa-3 / Esclerosis Múltiple / Neuronas Límite: Animals / Humans Idioma: En Revista: Sci Rep Año: 2020 Tipo del documento: Article País de afiliación: España

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Proteína 1 Similar a Quitinasa-3 / Esclerosis Múltiple / Neuronas Límite: Animals / Humans Idioma: En Revista: Sci Rep Año: 2020 Tipo del documento: Article País de afiliación: España