Ogihara M
Biochemical Pharmacology Group, Faculty of Pharmaceutical Sciences, Josai University, Japan.
Biol Pharm Bull. 1996 Apr;19(4):518-24. doi: 10.1248/bpb.19.518.
Effects of epidermal growth factor (EGF) on the expression of alpha(2)-adrenergic responses were examined in primary cultures of adult rat hepatocytes. The alpha(2)-responses were assessed by the inhibition of the rate of forskolin-stimulated cAMP formation by the selective alpha(2)-adrenergic agonists, oxymetazoline and UK-14304. Hepatocytes cultured with EGF (20 ng/ml) at a high cell density (1.0 x 10(5)/cm2) showed almost no response to the alpha(2)-adrenergic agonists, oxymetazoline and UK-14304 (1-100 mu M). In contrast, when cultured at a low cell density (3.3 x 10(4) cells/cm2) with EGF, forskolin-stimulated cAMP production was inhibited by oxymetazoline and UK-14304 in a dose-dependent manner. The alpha(2)-response was blocked by the alpha2-antagonist yohimbine (10 mu M). It was also reversed by treatment of hepatocytes with pertussis toxin (100 ng/ml). In addition, the effects of EGF on the appearance of alpha(2)-responses were almost completely inhibited by treatment of the hepatocytes with genistein (10 mu M) or cytochalasin B (10 mu M). The alpha(2)-response was abolished when cycloheximide (5 mu M) was added to the cultures. These results demonstrate that when cultured at a low cell density with EGF, adult rat hepatocytes acquire a significant alpha(2)-adrenergic response. The expression of this alpha(2)-response is associated with de novo protein synthesis.
在成年大鼠肝细胞原代培养物中检测了表皮生长因子(EGF)对α₂ - 肾上腺素能反应表达的影响。通过选择性α₂ - 肾上腺素能激动剂奥昔麻黄碱和UK - 14304对福司可林刺激的环磷酸腺苷(cAMP)形成速率的抑制作用来评估α₂ - 反应。在高细胞密度(1.0×10⁵个/cm²)下用EGF(20 ng/ml)培养的肝细胞对α₂ - 肾上腺素能激动剂奥昔麻黄碱和UK - 14304(1 - 100 μM)几乎无反应。相反,当在低细胞密度(3.3×10⁴个细胞/cm²)下用EGF培养时,福司可林刺激的cAMP产生受到奥昔麻黄碱和UK - 14304的剂量依赖性抑制。α₂ - 反应可被α₂ - 拮抗剂育亨宾(10 μM)阻断,也可被百日咳毒素(100 ng/ml)处理肝细胞后逆转。此外,用染料木黄酮(10 μM)或细胞松弛素B(10 μM)处理肝细胞几乎完全抑制了EGF对α₂ - 反应出现的影响。当向培养物中加入环己酰亚胺(5 μM)时,α₂ - 反应消失。这些结果表明,成年大鼠肝细胞在低细胞密度下用EGF培养时会获得显著的α₂ - 肾上腺素能反应。这种α₂ - 反应的表达与从头蛋白质合成有关。