Anisoosmotic regulation of hepatic gene expression.

U Warskulat, W Newsome, B Noe, B Stoll, D Haussinger
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引用次数: 30

Abstract

The effect of anisoosmolarity on the abundance of various mRNA species was examined in perfused rat liver and H4IIE rat hepatoma cells. Hyperosmotic exposure (385 mosmol/l) of isolated rat livers increased mRNA levels for tyrosine aminotransferase (TAT) by 246% and those for phosphoenolpyruvate carboxykinase (PEPCK) by 186%, whereas hypoosmotic exposure (225 mosmol/l) decreased their levels to 43% and 42%, respectively. mRNA levels for fructose-1,6-bisphosphatase (FBP), argininosuccinate lyase (ASL), argininosuccinate synthetase (ASS), glutamine synthetase (GS), glutaminase (GA) and glucokinase (GK) were largely unaffected. In H4IIE cells the modulation of TAT and PEPCK mRNA levels by anisoosmotic exposure was similar to that found in perfused rat liver. ASL and glutaminase mRNA levels were influenced in an opposite manner. The effects of anisoosmolarity on PEPCK mRNA levels in H4IIE cells were largely abolished in the presence of the protein kinase inhibitors H-7, H-89 and HA-1004. Other protein kinase inhibitors such as Go-6850, KN-62, Rp-8-CPT-cAMPS, rapamycin, wortmannin, genistein or herbimycin did not prevent the osmosensitivity of PEPCK mRNA levels. Also pertussis and cholera toxin, vanadate and colchicine did not affect the osmosensitivity of PEPCK mRNA levels. The data suggest that anisoosmotic exposure acts on the levels of some but not all mRNA species and that this action may involve changes in protein phosphorylation. They further indicate that the recently identified osmosensitive signal transduction pathway which involves a G-protein and tyrosine kinase dependent activation of mitogen-activated protein kinases is apparently not involved in the osmoregulation of PEPCK mRNA levels.

肝脏基因表达的各向同性调控。
在灌注的大鼠肝脏和H4IIE大鼠肝癌细胞中检测了异渗浓度对各种mRNA种类丰度的影响。高渗暴露(385 mosmol/l)使离体大鼠肝脏酪氨酸转氨酶(TAT) mRNA水平升高246%,磷酸烯醇丙酮酸羧激酶(PEPCK) mRNA水平升高186%,而低渗暴露(225 mosmol/l)使其水平分别降低43%和42%。果糖-1,6-二磷酸酶(FBP)、精氨酸琥珀酸裂解酶(ASL)、精氨酸琥珀酸合成酶(ASS)、谷氨酰胺合成酶(GS)、谷氨酰胺酶(GA)和葡萄糖激酶(GK) mRNA水平基本未受影响。在H4IIE细胞中,等渗暴露对TAT和PEPCK mRNA水平的调节与灌注大鼠肝脏相似。ASL和谷氨酰胺酶mRNA水平受到相反的影响。在蛋白激酶抑制剂H-7、H-89和HA-1004的存在下,不同浓度对H4IIE细胞PEPCK mRNA水平的影响基本被消除。其他蛋白激酶抑制剂如Go-6850、KN-62、Rp-8-CPT-cAMPS、雷帕霉素、wortmannin、染料木素或herbyycin均不能阻止PEPCK mRNA水平的渗透敏感性。百日咳和霍乱毒素、钒酸盐和秋水仙碱也不影响PEPCK mRNA水平的渗透敏感性。数据表明,异渗暴露作用于一些但不是所有mRNA物种的水平,这种作用可能涉及蛋白质磷酸化的变化。他们进一步表明,最近发现的渗透敏感信号转导通路涉及g蛋白和酪氨酸激酶依赖于有丝分裂原活化蛋白激酶的激活,显然不参与PEPCK mRNA水平的渗透调节。
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