Your browser doesn't support javascript.
loading
SHP-1 ameliorates nonalcoholic steatohepatitis by inhibiting proinflammatory cytokine production.
Lin, Lin; Jian, Jie; Song, Chun-Yan; Chen, Fei; Ding, Kai; Xie, Wei-Fen; Hu, Ping-Fang.
Afiliación
  • Lin L; Department of Gastroenterology, Changzheng Hospital, Second Military Medical University, Shanghai, China.
  • Jian J; Department of Gastroenterology, Changzheng Hospital, Second Military Medical University, Shanghai, China.
  • Song CY; Department of Gastroenterology, The First Affiliated Hospital of Nanchang University, Nanchang, China.
  • Chen F; Department of Pathology, Changhai Hospital, Second Military Medical University, Shanghai, China.
  • Ding K; Department of Gastroenterology, Changzheng Hospital, Second Military Medical University, Shanghai, China.
  • Xie WF; Department of Gastroenterology, Changzheng Hospital, Second Military Medical University, Shanghai, China.
  • Hu PF; Department of Gastroenterology, Changzheng Hospital, Second Military Medical University, Shanghai, China.
FEBS Lett ; 594(18): 2965-2974, 2020 09.
Article en En | MEDLINE | ID: mdl-32619269
ABSTRACT
Inflammation is the main contributor for the pathogenesis of nonalcoholic steatohepatitis (NASH). Src homology region 2 domain-containing phosphatase 1 (SHP-1, also known as PTPN6) is regarded as a negative regulator of inflammation, but its role in NASH remains unknown. Here, hepatocyte-specific Ptpn6 knockout mice (Ptpn6HKO ) and adenovirus vector-mediated ectopic expression of SHP-1 (AdSHP1) were used to evaluate the role of SHP-1 in a methionine- and choline-deficient diet-induced NASH model. Compared with the control littermates, Ptpn6HKO mice show exacerbated hepatic steatosis, inflammation, and fibrosis. Additionally, administration of AdSHP1 significantly ameliorates steatohepatitis and inhibits the expression of proinflammatory cytokines, including transforming growth factor-ß, interleukin-6, and tumor necrosis factor-α. Our data indicate that SHP-1 could be a potential therapeutic target for NASH.
Asunto(s)
Palabras clave

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Citocinas / Proteína Tirosina Fosfatasa no Receptora Tipo 6 / Enfermedad del Hígado Graso no Alcohólico Tipo de estudio: Prognostic_studies Límite: Animals Idioma: En Revista: FEBS Lett Año: 2020 Tipo del documento: Article País de afiliación: China

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Citocinas / Proteína Tirosina Fosfatasa no Receptora Tipo 6 / Enfermedad del Hígado Graso no Alcohólico Tipo de estudio: Prognostic_studies Límite: Animals Idioma: En Revista: FEBS Lett Año: 2020 Tipo del documento: Article País de afiliación: China