Wang Liyang, Xu MengMeng, Jones Odell D, Li Zhongguang, Liang Yu, Yu Qiuxia, Li Jiali, Wu Yajun, Lei Xinjuan, He Boling, Yue Huimin, Xiao Liqin, Zhou Rong, Zhang Wei, Zhou Xin, Zhang Yuhui, Bryant Joseph L, Ma Jianjie, Liu Yingli, Xu Xuehong
Key Laboratory of the Ministry of Education for Medicinal Resources and Natural Pharmaceutical Chemistry, National Engineering Laboratory for Resource Development of Endangered Crude Drugs in Northwest of China, Xi'an, 710062 China.
2Laboratory of Cell Biology, Genetics and Developmental Biology, Shaanxi Normal University College of Life Sciences, Xi'an, 710062 China.
Cell Biosci. 2020 Apr 6;10:55. doi: 10.1186/s13578-020-00414-2. eCollection 2020.
In the past 30 years, incidences of non-alcoholic fatty liver disease (NAFLD) has risen by 30%. However, there is still no clear mechanism or accurate method of anticipating liver failure. Here we reveal the phase transitions of liquid crystalline qualities in hepatic lipid droplets (HLDs) as a novel method of anticipating prognosis.
NAFLD was induced by feeding C57BL/6J mice on a high-fat (HiF) diet. These NAFLD livers were then evaluated under polarized microscopy, X-ray diffraction and small-angle scattering, lipid component chromatography analysis and protein expression analysis. Optically active HLDs from mouse model and patient samples were both then confirmed to have liquid crystal characteristics. Liver MAP1LC3A expression was then evaluated to determine the role of autophagy in liquid crystal HLD (LC-HLD) formation.
Unlike the normal diet cohort, HiF diet mice developed NAFLD livers containing HLDs exhibiting Maltese cross birefringence, phase transition, and fluidity signature to liquid crystals. These LC-HLDs transitioned to anisotropic crystal at 0 °C and remain crystalline. Temperature increase to 42 °C causes both liquid crystal and crystal HLDs to convert to isotropic droplet form. These isotropic HLDs successfully transition to anisotropic LC with fast temperature decrease and anisotropic crystal with slow temperature decrease. These findings were duplicated in patient liver. Patient LC-HLDs with no inner optical activity were discovered, hinting at lipid saturation as the mechanism through which HLD acquire LC characteristics. Downregulation of MAP1LC3A in conjunction with increased LC-HLD also implicated autophagy in NAFLD LC-HLD formation.
Increasing concentrations of amphiphilic lipids in HLDs favors organization into alternating hydrophilic and hydrophobic layers, which present as LC-HLDs. Thus, evaluating the extent of liquid crystallization with phase transition in HLDs of NAFLD patients may reveal disease severity and predict impending liver damage.
在过去30年中,非酒精性脂肪性肝病(NAFLD)的发病率上升了30%。然而,对于肝衰竭仍没有明确的机制或准确的预测方法。在此,我们揭示肝脂质滴(HLD)中液晶性质的相变作为一种预测预后的新方法。
通过给C57BL/6J小鼠喂食高脂(HiF)饮食诱导NAFLD。然后在偏光显微镜、X射线衍射和小角散射、脂质成分色谱分析和蛋白质表达分析下评估这些NAFLD肝脏。接着证实来自小鼠模型和患者样本的具有光学活性的HLD均具有液晶特性。然后评估肝脏微管相关蛋白1轻链3α(MAP1LC3A)的表达,以确定自噬在液晶HLD(LC-HLD)形成中的作用。
与正常饮食组不同,HiF饮食小鼠发生的NAFLD肝脏含有表现出马耳他十字双折射、相变和液晶流动性特征的HLD。这些LC-HLD在0°C时转变为各向异性晶体并保持结晶状态。温度升高到42°C会使液晶HLD和晶体HLD都转变为各向同性液滴形式。这些各向同性HLD在温度快速下降时成功转变为各向异性液晶,在温度缓慢下降时转变为各向异性晶体。这些发现也在患者肝脏中得到了重复。发现了没有内部光学活性的患者LC-HLD,这暗示脂质饱和是HLD获得LC特性的机制。MAP1LC3A的下调以及LC-HLD的增加也表明自噬参与了NAFLD中LC-HLD的形成。
HLD中两亲性脂质浓度的增加有利于组织成交替的亲水和疏水层,表现为LC-HLD。因此,评估NAFLD患者HLD中相变的液晶化程度可能揭示疾病严重程度并预测即将发生的肝损伤。