Your browser doesn't support javascript.
loading
Caveolin-1 deficiency alleviates palmitate-induced intracellular lipid accumulation and inflammation in pancreatic ß cells.
Zeng, Wen; Cai, Nan; Liu, Jia; Liu, Kunying; Lin, Shuo; Zeng, Longyi.
Afiliación
  • Zeng W; Department of Endocrinology and Metabolism, The Third Affiliated Hospital of Sun Yat-Sen University, Guangzhou, 510630, Guangdong, China.
  • Cai N; Guangdong Provincial Key Laboratory of Diabetology, The Third Affiliated Hospital of Sun Yat-Sen University, Guangzhou, 510630, Guangdong, China.
  • Liu J; Guangzhou Municipal Key Laboratory of Mechanistic and Translational Obesity Research, The Third Affiliated Hospital of Sun Yat-Sen University, Guangzhou, 510630, Guangdong, China.
  • Liu K; Medical Center for Comprehensive Weight Control, The Third Affiliated Hospital of Sun Yat-Sen University, Guangzhou, 510630, Guangdong, China.
  • Lin S; Department of Endocrinology and Metabolism, The Third Affiliated Hospital of Sun Yat-Sen University, Guangzhou, 510630, Guangdong, China.
  • Zeng L; Guangdong Provincial Key Laboratory of Diabetology, The Third Affiliated Hospital of Sun Yat-Sen University, Guangzhou, 510630, Guangdong, China.
J Physiol Biochem ; 80(1): 175-188, 2024 Feb.
Article en En | MEDLINE | ID: mdl-38032518
Lipotoxicity-induced pancreatic ß cell damage is a strong predictor of type 2 diabetes mellitus (T2DM). Our previous work showed that Caveolin-1 (Cav-1) depletion decreased ß-cell apoptosis and improved ß-cell viability. Further microarray analysis indicated significant changes in the expression of genes related to fatty acid metabolism and inflammation. The objective of this study was to explore the role of Cav-1 in intracellular lipid accumulation and inflammation in ß cells under lipotoxic conditions. Here, we established a ß-cell-specific Cav-1 knockout (ß-Cav-1 KO) mouse model and a CAV-1 depleted ß cell line (NIT-1). We found that Cav-1 silencing significantly reduced palmitate (PA)-induced intracellular triglyceride (TG) accumulation and decreased proinflammatory factor expression in both the mouse and cell models. Further mechanistic investigation revealed that amelioration of lipid metabolism was achieved through the downregulation of lipogenic markers (SREBP-1c, FAS and ACC) and upregulation of a fatty acid oxidation marker (CPT-1). Meanwhile, decrease of inflammatory cytokines (IL-6, TNF-α, and IL-1ß) secretion was found with the involvement of the IKKß/NF-κB signaling pathways. Our findings suggest that Cav-1 is of considerable importance in regulating lipotoxicity-induced ß-cell intracellular lipid accumulation and inflammation.
Asunto(s)
Palabras clave

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Diabetes Mellitus Tipo 2 / Células Secretoras de Insulina Límite: Animals Idioma: En Revista: J Physiol Biochem Asunto de la revista: BIOQUIMICA / FISIOLOGIA Año: 2024 Tipo del documento: Article País de afiliación: China Pais de publicación: España

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Diabetes Mellitus Tipo 2 / Células Secretoras de Insulina Límite: Animals Idioma: En Revista: J Physiol Biochem Asunto de la revista: BIOQUIMICA / FISIOLOGIA Año: 2024 Tipo del documento: Article País de afiliación: China Pais de publicación: España