Jirkovská Marie, Majer Filip, Smídová Jaroslava, Stríteský Jan, Shaik Gouse Mohiddin, Dráber Petr, Vítek Libor, Marecek Zdenek, Smíd Frantisek
Institute of Histology and Embryology, Prague, Czech Republic.
Glycoconj J. 2007 Jul;24(4-5):231-41. doi: 10.1007/s10719-007-9030-7. Epub 2007 Feb 27.
(Glyco)sphingolipids (GSL) are believed to protect the cell against harmful environmental factors by increasing the rigidity of plasma membrane. Marked decrease of membrane fluidity in cholestatic hepatocytes was described but the role of GSL therein has not been investigated so far. In this study, localization in hepatocytes of a representative of GSL, the GM1 ganglioside, was compared between of rats with cholestasis induced by 17alpha-ethinylestradiol (EE) and vehicle propanediol treated or untreated animals. GM1 was monitored by histochemical reaction employing cholera toxin B-subunit. Our findings in normal rat liver tissue showed that GM1 was localized in sinusoidal and canalicular hepatocyte membranes in both peripheral and intermediate zones of the hepatic lobules, and was nearly absent in central zones. On the contrary, in EE-treated animals GM1 was also expressed in central lobular zones. Moreover, detailed densitometry analysis at high magnification showed greater difference of GM1 expression between sinusoidal surface areas and areas of adjacent cytoplasm, caused as well by increased sinusoidal staining in central lobular zone as by decreased staining in cytoplasm in peripheral zone. These differences correlated with serum bile acids as documented by linear regression analyses. Both GM1 content and mRNA corresponding to GM1-synthase remained unchanged in livers; the enhanced expression of GM1 at sinusoidal membrane thus seems to be due to re-distribution of cellular GM1 at limited biosynthesis and could be responsible for protection of hepatocytes against harmful effects of bile acids accumulated during cholestasis.
(糖)鞘脂(GSL)被认为可通过增加质膜的刚性来保护细胞免受有害环境因素的影响。已有文献报道胆汁淤积性肝细胞的膜流动性显著降低,但GSL在其中的作用迄今尚未得到研究。在本研究中,比较了用17α-乙炔雌二醇(EE)诱导胆汁淤积的大鼠与用丙二醇载体处理或未处理的动物的肝细胞中GSL的一种代表性物质GM1神经节苷脂的定位情况。采用霍乱毒素B亚基的组织化学反应监测GM1。我们在正常大鼠肝脏组织中的研究结果表明,GM1定位于肝小叶外周和中间区的窦状隙和胆小管肝细胞细胞膜中,而中央区几乎不存在。相反,在EE处理的动物中,GM1在中央小叶区也有表达。此外,高倍镜下的详细光密度分析显示,窦状隙表面积与相邻细胞质区域之间GM1表达的差异更大,这是由中央小叶区窦状隙染色增加以及外周区细胞质染色减少所致。线性回归分析表明,这些差异与血清胆汁酸相关。肝脏中GM1含量和与GM1合成酶对应的mRNA均保持不变;因此,窦状隙膜上GM1表达的增强似乎是由于细胞GM1在有限生物合成过程中的重新分布,并且可能负责保护肝细胞免受胆汁淤积期间积累的胆汁酸的有害影响。