Fukushima Y, Matsuhashi N, Saitoh T, Mori H, Kodama T, Sugano K, Yazaki Y
Third Department of Internal Medicine, Faculty of Medicine, University of Tokyo, Japan.
J Gastroenterol. 1994 Jul;29 Suppl 7:68-72.
Canine histamine H2 receptor DNA, cloned by polymenase chain reaction (PCR), was transfected into Chinese hamster ovary cells using an expression vector. The expression of H2 receptors was demonstrated by immunoblotting with specific antibodies and the binding of tiotidine, an H2 receptor antagonist. H2 receptor-specific cAMP production was observed only in cells expressing canine H2 receptors. Preincubation of transfected cells with 10 microM histamine for 10 or 60 min at 37 degrees C decreased both the maximal response and the sensitivity of the subsequent histamine-stimulated cAMP production, showing desensitization. Under these circumstances, decreases in tiotidine binding without changes in affinity in intact cells and also in the membrane were observed, whereas there was no decrease in total H2 receptor number. Thus, desensitization of histamine H2 receptor was associated with the sequetration of receptors.
通过聚合酶链反应(PCR)克隆的犬组胺H2受体DNA,使用表达载体转染到中国仓鼠卵巢细胞中。用特异性抗体进行免疫印迹以及H2受体拮抗剂替丁的结合证明了H2受体的表达。仅在表达犬H2受体的细胞中观察到H2受体特异性cAMP的产生。将转染细胞在37℃下用10μM组胺预孵育10或60分钟,会降低随后组胺刺激的cAMP产生的最大反应和敏感性,表现出脱敏作用。在这些情况下,观察到完整细胞和膜中替丁结合减少而亲和力不变,而总H2受体数量没有减少。因此,组胺H2受体的脱敏与受体的隔离有关。