Newsome W P, Warskulat U, Noe B, Wettstein M, Stoll B, Gerok W, Häussinger D
Medizinische Universitätsklinik Freiburg, Federal Republic of Germany.
Biochem J. 1994 Dec 1;304 ( Pt 2)(Pt 2):555-60. doi: 10.1042/bj3040555.
Exposure of isolated perfused rat livers to hypo-osmotic (225 mosmol/l) perfusion media for 3 h led to a decrease of about 60% in mRNA levels for phosphoenolpyruvate carboxy-kinase (PEPCK) compared with normo-osmotic (305 mosmol/l) perfusions. Conversely, PEPCK mRNA levels increased about 3-fold during hyperosmotic (385 mosmol/l) perfusions. The anisotonicity effects were not explained by changes in the intracellular cyclic AMP (cAMP) concentration or by changes of the extracellular Na+ or Cl- activity. Similar effects of aniso-osmolarity on PEPCK mRNA levels were found in cultured rat hepatoma H4IIE.C3 cells, the experimental system used for further characterization of the effect. Whereas during the first hour of anisotonic exposure no effects on PEPCK mRNA levels were detectable, near-maximal aniso-osmolarity effects were observed within the next 2-3 h. PEPCK mRNA levels increased sigmoidally with the osmolarity of the medium, and the anisotonicity effects were most pronounced upon modulation of osmolarity between 250 and 350 mosmol/l. The aniso-osmolarity effects on PEPCK mRNA were not affected in presence of Gö 6850, protein kinase C inhibitor. cAMP increased the PEPCK mRNA levels about 2.3-fold in normo-osmotic media, whereas insulin lowered the PEPCK mRNA levels to about 8%. The effects of cAMP and insulin were also observed during hypo-osmotic and hyperosmotic exposure, respectively, but the anisotonicity effects were not abolished in presence of the hormones. The data suggest that hepatocellular hydration affects hepatic carbohydrate metabolism also over a longer term by modulating PEPCK mRNA levels. This is apparently unrelated to protein kinase C or alterations of cAMP levels. The data strengthen the view that cellular hydration is an important determinant for cell metabolic function by extending its regulatory role in carbohydrate metabolism to the level of mRNA.
将分离灌注的大鼠肝脏暴露于低渗(225毫渗摩尔/升)灌注介质中3小时,与等渗(305毫渗摩尔/升)灌注相比,磷酸烯醇丙酮酸羧激酶(PEPCK)的mRNA水平下降了约60%。相反,在高渗(385毫渗摩尔/升)灌注期间,PEPCK的mRNA水平增加了约3倍。细胞内环磷酸腺苷(cAMP)浓度的变化、细胞外Na+或Cl-活性的变化均无法解释这种渗透压变化的影响。在培养的大鼠肝癌H4IIE.C3细胞中也发现了等渗变化对PEPCK mRNA水平的类似影响,该实验系统用于进一步表征这种影响。在等渗暴露的第一个小时内,未检测到对PEPCK mRNA水平的影响,而在接下来的2 - 3小时内观察到了接近最大的等渗效应。PEPCK mRNA水平随培养基渗透压呈S形增加,在渗透压在250至350毫渗摩尔/升之间调节时,等渗效应最为明显。蛋白激酶C抑制剂Gö 6850存在时,等渗变化对PEPCK mRNA的影响不受影响。在等渗培养基中,cAMP使PEPCK mRNA水平增加约2.3倍,而胰岛素使PEPCK mRNA水平降至约8%。在低渗和高渗暴露期间也分别观察到了cAMP和胰岛素的作用,但在激素存在的情况下,等渗效应并未消除。数据表明,肝细胞水合作用还通过调节PEPCK mRNA水平在更长时间内影响肝脏碳水化合物代谢。这显然与蛋白激酶C或cAMP水平的改变无关。这些数据通过将其在碳水化合物代谢中的调节作用扩展到mRNA水平,强化了细胞水合作用是细胞代谢功能重要决定因素的观点。