作者
Jorge Simón,Maitane Núñez-García,Pablo Fernández‐Tussy,Lucía Barbier‐Torres,David Fernández‐Ramos,Beatriz Gómez‐Santos,Xabier Buqué,Fernando Lopitz‐Otsoa,Naroa Goikoetxea‐Usandizaga,Marina Serrano‐Maciá,Rubén Rodríguez‐Agudo,Maider Bizkarguenaga,Imanol Zubiete‐Franco,Virginia Gutiérrez‐de Juan,Diana Cabrera,Cristina Alonso,Paula Iruzubieta,Manuel Romero‐Gómez,Sebastiaan van Liempd,Azucena Castro,Rubén Nogueiras,Marta Varela‐Rey,Juan Manuel Falcón‐Pérez,Erica Villa,Javier Crespo,Shelly C. Lu,José M. Mato,Patricia Aspichueta,Teresa C. Delgado,María Luz Martínez‐Chantar
摘要
Simon et al. show that the glutaminase GLS1 isoform is augmented in both NASH clinical biopsies and pre-clinical mouse models. GLS1 silencing significantly reduced steatosis and oxidative stress through complex metabolic reprogramming, involving increased VLDL export, indicating that GLS1 may be a valuable therapeutic target for the treatment of NASH.