Department of Biological Chemistry, Weizmann Institute of Science, Rehovot 76100, Israel.
J Biol Chem. 2010 Apr 2;285(14):10911-23. doi: 10.1074/jbc.M109.077610. Epub 2010 Jan 28.
We have generated a mouse that cannot synthesize very long acyl chain (C22-C24) ceramides (Pewzner-Jung, Y., Park, H., Laviad, E. L., Silva, L. C., Lahiri, S., Stiban, J., Erez-Roman, R., Brugger, B., Sachsenheimer, T., Wieland, F. T., Prieto, M., Merrill, A. H., and Futerman, A. H. (2010) J. Biol. Chem. 285, 10902-10910) due to ablation of ceramide synthase 2 (CerS2). As a result, significant changes were observed in the sphingolipid profile of livers from these mice, including elevated C16-ceramide and sphinganine levels. We now examine the functional consequences of these changes. CerS2 null mice develop severe nonzonal hepatopathy from about 30 days of age, the age at which CerS2 expression peaks in wild type mice, and display increased rates of hepatocyte apoptosis and proliferation. In older mice there is extensive and pronounced hepatocellular anisocytosis with widespread formation of nodules of regenerative hepatocellular hyperplasia. Progressive hepatomegaly and noninvasive hepatocellular carcinoma are also seen from approximately 10 months of age. Even though CerS2 is found at equally high mRNA levels in kidney and liver, there are no changes in renal function and no pathological changes in the kidney. High throughput analysis of RNA expression in liver revealed up-regulation of genes associated with cell cycle regulation, protein transport, cell-cell interactions and apoptosis, and down-regulation of genes associated with intermediary metabolism, such as lipid and steroid metabolism, adipocyte signaling, and amino acid metabolism. In addition, levels of the cell cycle regulator, the cyclin dependent-kinase inhibitor p21(WAF1/CIP1), were highly elevated, which occurs by at least two mechanisms, one of which may involve p53. We propose a functional rationale for the synthesis of sphingolipids with very long acyl chains in liver homeostasis and in cell physiology.
我们生成了一种不能合成非常长链酰基(C22-C24)神经酰胺的小鼠(Pewzner-Jung,Y.,Park,H.,Laviad,E. L.,Silva,L. C.,Lahiri,S.,Stiban,J.,Erez-Roman,R.,Brugger,B.,Sachsenheimer,T.,Wieland,F. T.,Prieto,M.,Merrill,A. H.,和 Futerman,A. H.(2010)J. Biol. Chem. 285,10902-10910),这是由于鞘氨醇合酶 2(CerS2)的缺失。因此,这些小鼠肝脏的鞘脂谱发生了显著变化,包括 C16-神经酰胺和神经酰胺水平升高。现在我们检查这些变化的功能后果。CerS2 缺失的小鼠从大约 30 天龄开始发展为严重的非区域性肝病变,这是野生型小鼠 CerS2 表达的高峰年龄,并显示出更高的肝细胞凋亡和增殖率。在年龄较大的小鼠中,广泛形成再生性肝细胞增生的结节,广泛存在明显的肝细胞大小不均。大约从 10 个月龄开始,还会出现进行性肝肿大和非侵入性肝细胞癌。尽管 CerS2 在肾脏和肝脏中的 mRNA 水平同样高,但肾脏功能没有变化,肾脏也没有病理变化。肝脏中 RNA 表达的高通量分析显示,与细胞周期调控、蛋白质转运、细胞-细胞相互作用和细胞凋亡相关的基因上调,与中间代谢相关的基因下调,如脂质和类固醇代谢、脂肪细胞信号转导和氨基酸代谢。此外,细胞周期调节剂 cyclin 依赖性激酶抑制剂 p21(WAF1/CIP1)的水平高度升高,至少有两种机制导致这种情况,其中一种可能涉及 p53。我们提出了在肝脏稳态和细胞生理学中非常长链酰基神经酰胺合成的功能原理。