Kühn B, Schmid A, Harteneck C, Gudermann T, Schultz G
Institute of Pharmacology, Free University of Berlin, Germany.
Mol Endocrinol. 1996 Dec;10(12):1697-707. doi: 10.1210/mend.10.12.8961278.
In several cell systems histamine has been shown to stimulate both adenylyl cyclase and phospholipase C through activation of a G protein-coupled H2 receptor. To analyze the bifurcating signal emanating from the activated H2 receptor and to identify the G proteins involved, H1 and H2 histamine receptors were functionally expressed in baculovirus-infected insect cells. Histamine challenge lead to concentration-dependent cAMP formation and Ca2+ mobilization in Sf9 cells infected with a virus encoding the H2 receptor, whereas H1 receptor stimulation only resulted in pronounced phospholipase C activation. To analyze the G protein coupling pattern of histamine receptors, activated G proteins were labeled with [alpha-32P]GTP azidoanilide and identified by selective immunoprecipitation. In insect cell membranes expressing H1 histamine receptors, histamine led to incorporation of the label into alpha q-like proteins, whereas activation of the H2 receptor resulted in labeling of alpha q- and alpha s-like G protein alpha-subunits. In COS cells transfected with H2 receptor complementary DNA, histamine caused concentration-dependent accumulation of cAMP and inositol phosphates; the latter effect was insensitive to pertussis toxin treatment. Histamine stimulation led to a pronounced increase in inositol phosphate production when complementary DNAs coding for alpha q, alpha 11, alpha 14, or alpha 15 G protein alpha-subunits were cotransfected. This increase was specific for Gq family members, as overexpression of alpha 12 or alpha s did not enhance histamine-stimulated phospholipase C activation. In membranes of guinea pig heart, addition of [alpha-32P]GTP azidoanilide resulted in labeling of alpha q and alpha 11 via the activated H1 and also via H2 receptors. These data demonstrate that dual signaling of the activated H2 histamine receptor is mediated by coupling of the receptor to Gs and Gq family members.
在多个细胞系统中,组胺已被证明可通过激活G蛋白偶联的H2受体来刺激腺苷酸环化酶和磷脂酶C。为了分析来自活化H2受体的分支信号并鉴定所涉及的G蛋白,H1和H2组胺受体在杆状病毒感染的昆虫细胞中进行了功能表达。组胺刺激导致感染编码H2受体病毒的Sf9细胞中cAMP形成和Ca2+动员呈浓度依赖性,而H1受体刺激仅导致明显的磷脂酶C激活。为了分析组胺受体的G蛋白偶联模式,活化的G蛋白用[α-32P]GTP叠氮苯胺标记,并通过选择性免疫沉淀进行鉴定。在表达H1组胺受体的昆虫细胞膜中,组胺导致标记物掺入αq样蛋白,而H2受体的激活导致αq和αs样G蛋白α亚基的标记。在用H2受体互补DNA转染的COS细胞中,组胺导致cAMP和肌醇磷酸的浓度依赖性积累;后一种效应不受百日咳毒素处理的影响。当共转染编码αq、α11、α14或α15 G蛋白α亚基的互补DNA时,组胺刺激导致肌醇磷酸产生显著增加。这种增加对Gq家族成员具有特异性,因为α12或αs的过表达并未增强组胺刺激的磷脂酶C激活。在豚鼠心脏的膜中,添加[α-32P]GTP叠氮苯胺导致通过活化的H1以及通过H2受体对αq和α11进行标记。这些数据表明,活化的H2组胺受体的双重信号传导是由受体与Gs和Gq家族成员的偶联介导的。