脂肪变性
蛋白质亚单位
积分器
化学
内科学
医学
计算机科学
生物化学
电信
基因
带宽(计算)
作者
Minami Shiozaki,Keishi Kanno,Sayaka Yonezawa,Yuichiro Otani,Yuya Shigenobu,Daisuke Haratake,Eisuke Murakami,Shiro Oka,Masanori Ito
标识
DOI:10.1016/j.bbalip.2024.159532
摘要
Hepatic adipogenesis has common mechanisms with adipocyte differentiation such as PPARγ involvement and the induction of adipose tissue-specific molecules. A previous report demonstrated that integrator complex subunit 6 (INTS6) is required for adipocyte differentiation. This study aimed to investigate INTS6 expression and its role in hepatic steatosis progression. The expression of INTS6 and PPARγ was examined in the liver of a mouse model of steatohepatitis and in paired liver biopsy samples from 11 patients with severe obesity and histologically proven metabolic dysfunction associated steatohepatitis (MASH) before and one year after bariatric surgery. To induce hepatocellular steatosis in vitro, an immortalized human hepatocyte cell line Hc3716 was treated with free fatty acids. In the steatohepatitis mouse model, we observed hepatic induction of INTS6, PPARγ, and adipocyte-specific genes. In contrast, β-catenin which negatively regulates PPARγ was reduced. Biopsied human livers demonstrated a strong positive correlation (r
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