肝细胞特异性敲除 Na+/H+ 交换子-1 无法改善小鼠与 NASH 相关的肝损伤

Lise M. Sjøgaard-Frich, Cecilie M. Egeskov, Jens F. Halling, Muthulakshmi Ponniah, Oksana Dmytriyeva, Henriette Pilegaard, Stine Falsig Pedersen
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引用次数: 0

摘要

非酒精性脂肪肝(NAFLD)是与肝脏相关的死亡率增长最快的疾病,影响着全球约 25% 的成年人口。尽管如此,有关其根本机制的基本问题仍未得到完全解答。在小鼠中,Na+/H+交换子NHE1(SLC9A1)的全身基因敲除(KO)被认为对NASH具有保护作用。然而,由于全身 NHE1 KO 会影响肝脏以外组织的普遍过程,这一发现的可转化性受到了干扰。在此,我们旨在确定肝细胞 NHE1 在非酒精性脂肪肝中的作用。我们产生了一种肝细胞特异性 NHE1 KO(NHE1 HKO)小鼠,并确定了蛋氨酸-胆碱缺乏(MCD)饮食后 NHE1 缺失对肝脏代谢和非酒精性脂肪肝特征的影响。肝细胞 NHE1 的缺失并不能防止非酒精性脂肪肝的发生,反而会损害小鼠肝脏的 ROS 基础平衡。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Hepatocyte-Specific Knockout of Na+/H+ Exchanger-1 Does Not Ameliorate NASH-Associated Liver Damage in Mice

Hepatocyte-Specific Knockout of Na+/H+ Exchanger-1 Does Not Ameliorate NASH-Associated Liver Damage in Mice

Non-alcoholic fatty liver disease (NAFLD) is the fastest-growing liver-related cause of mortality, affecting about 25% of the adult world population. Despite this, fundamental questions regarding the underlying mechanisms remain incompletely answered. In mice, whole-body knockout (KO) of Na+/H+ exchanger NHE1 (SLC9A1) was suggested to be protective against NASH. However, the translatability of this finding is confounded by the fact that global NHE1 KO affects ubiquitous processes in tissues outside of the liver. Here, we aimed to determine the role of hepatocyte NHE1 in NAFLD. We generated a hepatocyte-specific NHE1 KO (NHE1 HKO) mouse and determined the impact of NHE1 loss on liver metabolism and NAFLD characteristics following methionine–choline-deficient (MCD) diet. Loss of hepatocyte NHE1 does not protect against NAFLD development, but rather seems to impair basal ROS balance in the mouse liver.

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