Zhu Wei, Zhang Meihua, Chang Liming, Zhu Wenbo, Li Cheng, Xie Feng, Zhang Huan, Zhao Tian, Jiang Jianping
1CAS Key Laboratory of Mountain Ecological Restoration and Bioresource Utilization & Ecological Restoration Biodiversity Conservation Key Laboratory of Sichuan Province, Chengdu Institute of Biology, Chengdu, 610041 China.
2University of Chinese Academy of Sciences, Beijing, 100049 China.
Front Zool. 2019 Nov 14;16:42. doi: 10.1186/s12983-019-0341-x. eCollection 2019.
Fat storage is required for the life cycle of many organisms. The primary fat depot for most vertebrates is white adipose tissue. However, in primitive vertebrates (e.g., agnathan group and elasmobranchs), the liver is usually responsible for fat storage. Among the vertebrates, amphibians have a unique status, as their larvae live in the water and exhibit some primitive traits that are similar to fish. Although it has been recognized that adult frogs use their abdominal white adipose tissue as a primary fat depot, how tadpoles store their fat is still inconclusive. The metabolic traits and physiological functions of primitive fat depots may have wide-ranging implications on the pathology of abnormal lipid deposition in mammals and the evolution of fat storage.
tadpoles used their liver as the primary fat depot. In sufficiently fed tadpoles at stage 30-31, the hepatosomatic index (HSI) reached up to 7%, and triglycerides (TG) accounted for 15% of liver weight. Their liver resembled white adipose tissue in histological morphology, characterized by polygonal hepatocytes filled with fat. Their liver metabolic composition was unique, characterized by the dominance of maltotriose, arachidonic acid and dipeptides in soluble carbohydrates, free fatty acids and amino acids. Hepatic fat was the major metabolic fuel of fasted tadpoles, which had similar reserve mobilization and allocation patterns as mammals. From a developmental perspective, hepatic fat was important to fuel late metamorphic climax. Interestingly, starvation induced accelerated metamorphosis in tadpoles with high HSI (4.96 ± 0.21%). However, this phenomenon was not observed in tadpoles with low HSI (2.71 ± 0.16%), even though they had similar initial body weight and developmental stage. Hepatic fat abundance was the most prominent difference between the two groups.
To the best of our knowledge, this is the first report that liver can be the primary fat depot in vertebrates with higher evolutionary status than bony fish. The unique hepatic histological and metabolic traits likely either guard their liver against lipotoxicity or make their hepatocytes adapt to fat accumulation. This fatty liver could be a primitive counterpart of mammalian white adipose tissue (WAT). In addition, our study showed that the hepatic reserves of tadpoles, especially TG content, may provide body condition signals to modulate metamorphosis.
脂肪储存是许多生物体生命周期所必需的。大多数脊椎动物的主要脂肪储存部位是白色脂肪组织。然而,在原始脊椎动物(如无颌类和软骨鱼类)中,肝脏通常负责脂肪储存。在脊椎动物中,两栖动物具有独特的地位,因为它们的幼体生活在水中,并表现出一些与鱼类相似的原始特征。尽管人们已经认识到成年青蛙将腹部白色脂肪组织作为主要脂肪储存部位,但蝌蚪如何储存脂肪仍尚无定论。原始脂肪储存部位的代谢特征和生理功能可能对哺乳动物异常脂质沉积的病理学以及脂肪储存的进化具有广泛影响。
蝌蚪将肝脏作为主要脂肪储存部位。在30 - 31期喂食充足的蝌蚪中,肝体指数(HSI)高达7%,甘油三酯(TG)占肝脏重量的15%。它们的肝脏在组织学形态上类似于白色脂肪组织,其特征是多边形肝细胞充满脂肪。它们肝脏的代谢组成独特,其特征是在可溶性碳水化合物、游离脂肪酸和氨基酸中,麦芽三糖、花生四烯酸和二肽占主导地位。肝脏脂肪是禁食蝌蚪的主要代谢燃料,其储备动员和分配模式与哺乳动物相似。从发育角度来看,肝脏脂肪对于为晚期变态高峰期提供能量很重要。有趣的是,饥饿会导致高HSI(4.96±0.21%)的蝌蚪加速变态。然而,在低HSI(2.71±0.16%)的蝌蚪中未观察到这种现象,尽管它们具有相似的初始体重和发育阶段。两组之间最显著的差异是肝脏脂肪丰度。
据我们所知,这是首次报道肝脏可以成为进化地位高于硬骨鱼的脊椎动物的主要脂肪储存部位。独特的肝脏组织学和代谢特征可能要么保护它们的肝脏免受脂毒性影响,要么使它们的肝细胞适应脂肪积累。这种脂肪肝可能是哺乳动物白色脂肪组织(WAT)的原始对应物。此外,我们的研究表明,蝌蚪的肝脏储备,尤其是TG含量,可能提供身体状况信号来调节变态。