Department of Internal Medicine, Kitasato University Medical Center, Kitamoto, Saitama, Japan
Department of Clinical Pharmacy, Kitasato University School of Pharmacy, Minato-ku, Tokyo, Japan.
BMJ Open Gastroenterol. 2020 May;7(1). doi: 10.1136/bmjgast-2019-000370.
Non-alcoholic steatohepatitis (NASH) can progress to fibrosis, cirrhosis and end-stage liver disease. Glucagon-like peptide 1 receptor (GLP-1R) mediates β cell function. Its receptor agonists, currently used to treat type 2 diabetes mellitus, might be effective against NASH. GLP-1R, a G protein-coupled receptor family member, preferentially localises to caveolae. Therefore, we ascertained the cellular localisation of GLP-1R and caveolin (CAV)-1 in NASH liver.
Liver biopsies were obtained from three patients with NASH and were compared with those of four normal patients. Immunohistochemistry (IHC) and immunoelectron microscopy (IEM) were used to compare GLP-1R and CAV-1 expression in the livers of patients with metastatic liver cancer and normal patients.
IHC showed that GLP-1R localised to basolateral membranes of hepatocytes with macrovesicular steatosis and was expressed in monocytes infiltrating hepatic sinusoids. CAV-1 was minimally associated with low-electron density lipid droplets (LDs) in hepatocytes. IEM showed small clusters of GLP-1R molecules on the peripheral rims of LDs and on cytoplasmic leaflets of endoplasmic reticulum membranes and vesicles, whereas CAV-1 molecules were found in LD caveolae.
GLP-1R is present in the lipid microdomains of hepatocytes with macrovesicular steatosis. These results may help inform future studies about the liver-specific mechanisms of GLP-1 modulation in NASH therapy.
非酒精性脂肪性肝炎(NASH)可进展为肝纤维化、肝硬化和终末期肝病。胰高血糖素样肽 1 受体(GLP-1R)介导β细胞功能。目前用于治疗 2 型糖尿病的其受体激动剂可能对 NASH 有效。GLP-1R 是 G 蛋白偶联受体家族成员,优先定位于 caveolae。因此,我们确定了 NASH 肝脏中 GLP-1R 和 caveolin(CAV)-1 的细胞定位。
从 3 例 NASH 患者和 4 例正常患者中获取肝活检。使用免疫组织化学(IHC)和免疫电子显微镜(IEM)比较转移性肝癌患者和正常患者肝脏中 GLP-1R 和 CAV-1 的表达。
IHC 显示 GLP-1R 定位于具有大泡性脂肪变性的肝细胞的基底外侧膜,并在浸润肝窦的单核细胞中表达。CAV-1 与肝细胞中的低电子密度脂质滴(LD)很少相关。IEM 显示 GLP-1R 分子在 LD 的外周边缘和内质网膜和小泡的细胞质小叶上形成小簇,而 CAV-1 分子存在于 LD caveolae 中。
GLP-1R 存在于具有大泡性脂肪变性的肝细胞的脂质微区中。这些结果可能有助于为未来关于 NASH 治疗中 GLP-1 调节的肝脏特异性机制的研究提供信息。