Department of Interdisciplinary Medicine (DIM), University of Bari "Aldo Moro", Bari, Italy.
Department of Translational Biomedicine and Neuroscience (DiBraiN), University of Bari "Aldo Moro", Bari, Italy.
Liver Int. 2024 Oct;44(10):2738-2752. doi: 10.1111/liv.16052. Epub 2024 Jul 24.
BACKGROUND & AIMS: Metabolic dysfunction-associated steatohepatitis (MASH) is a growing cause of chronic liver disease, characterized by fat accumulation, inflammation and fibrosis, which development depends on mitochondrial dysfunction and oxidative stress. Highly expressed in the liver during fasting, peroxisome proliferator-activated receptor-γ coactivator-1α (PGC-1α) regulates mitochondrial and oxidative metabolism. Given the relevant role of mitochondrial function in MASH, we investigated the relationship between PGC-1α and steatohepatitis.
We measured the hepatic expression of Pgc-1α in both MASH patients and wild-type mice fed a western diet (WD) inducing steatosis and fibrosis. We then generated a pure C57BL6/J strain loss of function mouse model in which Pgc-1α is selectively deleted in the liver and we fed these mice with a WD supplemented with sugar water that accurately mimics human MASH.
We observed that the hepatic expression of Pgc-1α is strongly reduced in MASH, in both humans and mice. Moreover, the hepatic ablation of Pgc-1α promotes a considerable reduction of the hepatic mitochondrial respiratory capacity, setting up a bioenergetic harmful environment for liver diseases. Indeed, the lack of Pgc-1α decreases mitochondrial function and increases inflammation, fibrosis and oxidative stress in the scenario of MASH. Intriguingly, this profibrotic phenotype is not linked with obesity, insulin resistance and lipid disbalance.
In a MASH model the hepatic ablation of Pgc-1α drives fibrosis independently from lipid and glucose metabolism. These results add a novel mechanistic piece to the puzzle of the specific and crucial role of mitochondrial function in MASH development.
代谢相关脂肪性肝炎(MASH)是一种日益增多的慢性肝病病因,其特征为脂肪堆积、炎症和纤维化,其发展取决于线粒体功能障碍和氧化应激。过氧化物酶体增殖物激活受体γ共激活因子 1α(PGC-1α)在空腹时在肝脏中高表达,调节线粒体和氧化代谢。鉴于线粒体功能在 MASH 中的相关作用,我们研究了 PGC-1α与脂肪性肝炎之间的关系。
我们测量了 MASH 患者和经西方饮食(WD)诱导脂肪变性和纤维化的野生型小鼠肝脏中 Pgc-1α的表达。然后,我们生成了一种纯 C57BL6/J 品系的功能丧失型小鼠模型,其中 Pgc-1α在肝脏中被选择性缺失,并给这些小鼠喂食添加糖水的 WD,这准确模拟了人类 MASH。
我们观察到,在人类和小鼠的 MASH 中,肝脏中 Pgc-1α的表达强烈降低。此外,肝脏中 Pgc-1α的缺失可显著降低肝脏线粒体呼吸能力,为肝脏疾病建立了一种有害的生物能量环境。事实上,缺乏 Pgc-1α可降低线粒体功能并增加炎症、纤维化和氧化应激在 MASH 中的作用。有趣的是,这种促纤维化表型与肥胖、胰岛素抵抗和脂质失衡无关。
在 MASH 模型中,肝脏中 Pgc-1α的缺失可独立于脂质和葡萄糖代谢驱动纤维化。这些结果为线粒体功能在 MASH 发展中的特定和关键作用的机制提供了新的认识。