Wu D, Katz A, Lee C H, Simon M I
Division of Biology, California Institute of Technology, Pasadena 91125.
J Biol Chem. 1992 Dec 25;267(36):25798-802.
High efficiency transient transfection of Cos-7 cells was previously used to establish the functional coupling between G alpha q/G alpha 11 and phospholipase C beta 1 (Wu, D., Lee, C-H., Rhee, S. G., and Simon, M. I. (1992) J. Biol. Chem. 267, 1811-1817). Here the same system was used to study the functional coupling between other guanine nucleotide-binding regulatory protein (G-protein) alpha subunits and phospholipases and to study which G alpha subunits mediate the activation of phospholipase C by the alpha 1-adrenergic receptor subtypes, alpha 1 A, alpha 1 B, and alpha 1 C. We found that G alpha 14 and G alpha 16 behaved like G alpha 11 or G alpha q, i.e. they could activate endogenous phospholipases in Cos-7 cells in the presence of AIFn. The synergistic increase in inositol phosphate release in Cos-7 cells after they were cotransfected with cDNAs encoding G alpha subunits and phospholipase C beta 1 indicates that both G alpha 16 and G alpha 14 can activate phospholipase C beta 1. The activation of phospholipase C beta 1 was restricted to members of the Gq subfamily of alpha subunits. They activated phospholipase C beta 1 but not phospholipase C gamma 1, gamma 2, or phospholipase C delta 3. The cotransfection of Cos-7 cells with cDNAs encoding three different alpha 1-adrenergic receptors and G alpha q or G alpha 11 leads to an increase in norepinephrine-dependent inositol phosphate release. This indicates that G alpha q or G alpha 11 can mediate the activation of phospholipase C by all three subtypes of alpha 1-adrenergic receptors. With the same assay system, G alpha 16 and G alpha 14 appear to be differentially involved in the activation of phospholipase C by the alpha 1-adrenergic receptors. The alpha 1 B subtype receptor gave a ligand-mediated synergistic response in the cells cotransfected with either G alpha 14 or G alpha 16. However, the alpha 1 C receptor responded in cells cotransfected with G alpha 14 but not G alpha 16, and the alpha 1 A receptor showed little synergistic response in cells transfected with either G alpha 14 or G alpha 16. The ability of the alpha 1 A and alpha 1 C receptors to activate phospholipase C through G alpha q and G alpha 11 was also demonstrated in a cell-free system.(ABSTRACT TRUNCATED AT 400 WORDS)
此前人们利用高效瞬时转染Cos-7细胞的方法来建立Gαq/Gα11与磷脂酶Cβ1之间的功能偶联(Wu, D., Lee, C-H., Rhee, S. G., and Simon, M. I. (1992) J. Biol. Chem. 267, 1811 - 1817)。在此,我们使用相同的系统来研究其他鸟嘌呤核苷酸结合调节蛋白(G蛋白)α亚基与磷脂酶之间的功能偶联,并研究哪些Gα亚基介导α1 - 肾上腺素能受体亚型α1A、α1B和α1C对磷脂酶C的激活作用。我们发现Gα14和Gα16的表现与Gα11或Gαq类似,即在存在AIFn的情况下,它们能激活Cos-7细胞中的内源性磷脂酶。Cos-7细胞在共转染编码Gα亚基的cDNA和磷脂酶Cβ1后,肌醇磷酸释放的协同增加表明Gα16和Gα14都能激活磷脂酶Cβ1。磷脂酶Cβ1的激活仅限于α亚基Gq亚家族的成员。它们激活磷脂酶Cβ1,但不激活磷脂酶Cγ1、γ2或磷脂酶Cδ3。Cos-7细胞共转染编码三种不同α1 - 肾上腺素能受体的cDNA与Gαq或Gα11,会导致去甲肾上腺素依赖性肌醇磷酸释放增加。这表明Gαq或Gα11可以介导所有三种α1 - 肾上腺素能受体亚型对磷脂酶C的激活。在相同的检测系统中,Gα16和Gα14在α1 - 肾上腺素能受体对磷脂酶C的激活中似乎有不同的参与情况。α1B亚型受体在与Gα14或Gα16共转染的细胞中产生配体介导的协同反应。然而,α1C受体在与Gα14共转染的细胞中有反应,而与Gα16共转染时无反应,并且α1A受体在与Gα14或Gα16共转染的细胞中几乎没有协同反应。α1A和α1C受体通过Gαq和Gα11激活磷脂酶C的能力在无细胞系统中也得到了证实。(摘要截选至400字)