肝细胞中与非酒精性脂肪性肝病相关基因 PNPLA3 的表达水平受肝脂质状态的影响很大。
The expression level of non-alcoholic fatty liver disease-related gene PNPLA3 in hepatocytes is highly influenced by hepatic lipid status.
机构信息
Division of Biopharmaceutics, Leiden/Amsterdam Center for Drug Research, Gorlaeus Laboratories, Leiden University, Leiden, The Netherlands.
出版信息
J Hepatol. 2010 Feb;52(2):244-51. doi: 10.1016/j.jhep.2009.11.004. Epub 2009 Nov 24.
BACKGROUND & AIMS: Recent studies have suggested that variations in PNPLA3 are associated with non-alcoholic fatty liver disease (NAFLD). To gain insight into the potential function of PNPLA3 in liver, we have determined the effect of metabolic shifts on the hepatic expression profile of PNPLA3 in mice.
METHODS
PNPLA3 expression in wild-type C57BL/6 and NAFLD-susceptible LDL receptor knockout (LDLR-/-) mice was determined using microarray and real-time PCR analysis.
RESULTS
PNPLA3 expression in livers is 50- to 100-fold lower as compared to (cardiac) muscle and adipose tissue in regular chow diet-fed mice. Feeding a Western-type diet stimulated hepatic relative PNPLA3 expression level 23-fold (p<0.001) both in C57BL/6 mice and LDLR-/- mice, suggesting that PNPLA3 does become an important player in hepatic lipid metabolism under conditions of lipid excess. Subjecting mice to fasting fully reversed the effect of the Western-type diet on hepatic PNPLA3 expression. Under these conditions, the expression level of PNPLA3 in adipose tissue is also decreased 90% (p<0.001). Cellular distribution analysis revealed that PNPLA3 is expressed in hepatocytes but not in liver endothelial and Kupffer cells. Microarray-based gene profiling showed that the expression level of PNPLA3 in hepatocytes is correlated with that of genes associated with the lipogenic pathway such as ME1, SPOT14, and SCD1.
CONCLUSIONS
It appears that the NAFLD-related gene PNPLA3 is highly responsive to metabolic changes in hepatocytes within the liver and its relative change in expression level suggests an essential function in lipogenesis.
背景与目的
最近的研究表明,PNPLA3 的变异与非酒精性脂肪性肝病(NAFLD)有关。为了深入了解 PNPLA3 在肝脏中的潜在功能,我们确定了代谢变化对小鼠肝脏中 PNPLA3 表达谱的影响。
方法
使用微阵列和实时 PCR 分析检测野生型 C57BL/6 和易患 NAFLD 的 LDL 受体敲除(LDLR-/-)小鼠中 PNPLA3 的表达。
结果
在常规饲料喂养的小鼠中,PNPLA3 在肝脏中的表达比(心脏)肌肉和脂肪组织低 50-100 倍。给予西方型饮食可刺激 C57BL/6 小鼠和 LDLR-/- 小鼠的肝相对 PNPLA3 表达水平增加 23 倍(p<0.001),表明 PNPLA3 在脂质过剩的情况下确实成为肝脏脂质代谢的重要参与者。使小鼠禁食完全逆转了西方型饮食对肝脏 PNPLA3 表达的影响。在这些条件下,脂肪组织中 PNPLA3 的表达水平也降低了 90%(p<0.001)。细胞分布分析表明,PNPLA3 表达于肝细胞,但不表达于肝内皮细胞和库普弗细胞。基于微阵列的基因谱分析显示,肝细胞中 PNPLA3 的表达水平与与脂肪生成途径相关的基因如 ME1、SPOT14 和 SCD1 的表达水平相关。
结论
似乎与 NAFLD 相关的基因 PNPLA3 对肝脏中肝细胞的代谢变化高度敏感,其相对表达水平变化提示其在脂肪生成中具有重要功能。