下调和上调
细胞内
化学
细胞生物学
生物化学
生物
基因
作者
Grazia Pennisi,Samantha Maurotti,Ester Ciociola,Oveis Jamialahmadi,Giorgio Bertolazzi,Angela Mirarchi,Per-Olof Bergh,Francesca Scionti,Rosellina Margherita Mancina,Rocco Spagnuolo,Claudio Tripodo,Jan Borén,Salvatore Petta,Stefano Romeo
标识
DOI:10.1161/atvbaha.123.319789
摘要
Background: ANGPTL3 (angiopoietin-like protein 3) is a circulating protein with a key role in maintaining lipoprotein homeostasis. A monoclonal antibody against ANGPTL3 is an approved and well-tolerated treatment to reduce lipoproteins in familial hypercholesterolemia homozygotes. However, the reduction of hepatic ANGPTL3 synthesis using an antisense oligonucleotide unexpectedly resulted in a dose-dependent increase in liver lipid content and circulating transaminases, resulting in the termination of the clinical trial. Meanwhile, the use of silencing RNAs remains an area of active investigation. Our study sought to investigate whether intracellular downregulation of ANGPTL3 may lead to a primary increase in neutral lipids within the hepatocyte. Methods: We downregulated ANGPTL3 by silencing RNA in primary human hepatocytes 3-dimensional spheroids, HepG2/LX-2 3-dimensional spheroids, and in HepG2, Hep3B2, and Huh7 cultured in 2 dimensions. Results: ANGPTL3 downregulation increased neutral lipids in all models investigated. Interestingly, ANGPTL3 induced lower intracellular deiodinase type 1 protein levels resulting in a reduction in beta-oxidation and causing an increase in triglycerides stored in lipid droplets. Conclusions: In conclusion, intracellular ANGPTL3 downregulation by silencing RNA led to an increase in triglycerides content due to a reduction in energy substrate utilization resembling a primary intracellular hepatocyte hypothyroidism.
科研通智能强力驱动
Strongly Powered by AbleSci AI