Moon Jieun, Kong Eunji, Lee Jingu, Jung Jinjoo, Kim Eunha, Park Seung Bum, Kim Pilhan
Graduate School of Nanoscience and Technology, Korea Advanced Institute of Science and Technology (KAIST), 291 Daehak-ro, Yuseong-gu, Daejeon, 34141, South Korea.
KI for Health Science and Technology (KIHST), Korea Advanced Institute of Science and Technology, (KAIST), 291 Daehak-ro, Yuseong-gu, Daejeon, 34141, South Korea.
Biomed Opt Express. 2020 Aug 19;11(9):5132-5146. doi: 10.1364/BOE.395890. eCollection 2020 Sep 1.
Nonalcoholic fatty liver disease (NAFLD) is a rapidly increasing chronic liver disorder worldwide accompanied by hepatic steatosis, inflammation, fibrosis, and severe liver failure. Unfortunately, an effective treatment strategy for NAFLD has not yet been established, which has been hampered by the limited understanding of the pathophysiological drivers for NAFLD. To examine the unknown cellular and molecular mechanisms in the pathogenesis of NAFLD, there is an increasing need for the direct observation of hepatic microenvironments over extended periods of time. In this work, using a custom-built intravital imaging system and a novel fluorescent lipid droplet labeling dye, Seoul-Fluor 44 (SF44), we established an intravital imaging method to visualize individual lipid droplets and microvasculature simultaneously in the liver of live mice . In addition, in the nonalcoholic steatosis and steatohepatitis mouse model induced by a methionine and choline-deficient diet, we longitudinally visualized and quantitatively analyzed the development of lipid droplets in hepatocytes and sinusoid at a subcellular resolution during the progression of NAFLD up to 21 days .
非酒精性脂肪性肝病(NAFLD)是一种在全球范围内迅速增加的慢性肝脏疾病,伴有肝脂肪变性、炎症、纤维化和严重肝衰竭。不幸的是,尚未建立有效的NAFLD治疗策略,对NAFLD病理生理驱动因素的有限理解阻碍了这一进展。为了研究NAFLD发病机制中未知的细胞和分子机制,越来越需要长时间直接观察肝脏微环境。在这项工作中,我们使用定制的活体成像系统和新型荧光脂滴标记染料首尔荧光44(SF44),建立了一种活体成像方法,可同时在活小鼠肝脏中可视化单个脂滴和微血管。此外,在由蛋氨酸和胆碱缺乏饮食诱导的非酒精性脂肪变性和脂肪性肝炎小鼠模型中,我们在NAFLD进展长达21天的过程中,以亚细胞分辨率纵向可视化并定量分析了肝细胞和肝血窦中脂滴的发展情况。