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首页> 外文期刊>Neurochemistry International: The International Journal for the Rapid Publication of Critical Reviews, Preliminary and Original Research Communications in Neurochemistry >Levels of Gsalpha(short and long), Galpha(olf) and Gbeta(common) subunits, and calcium-sensitive adenylyl cyclase isoforms (1, 5/6, 8) in post-mortem human brain caudate and cortical membranes: comparison with rat brain membranes and potential stoichiometric relationships.
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Levels of Gsalpha(short and long), Galpha(olf) and Gbeta(common) subunits, and calcium-sensitive adenylyl cyclase isoforms (1, 5/6, 8) in post-mortem human brain caudate and cortical membranes: comparison with rat brain membranes and potential stoichiometric relationships.

机译:人死后脑尾状和皮膜中Gsalpha(短和长),Galpha(olf)和Gbeta(常见)亚基的水平以及钙敏感的腺苷酸环化酶同工型(1、5 / 6、8):与大鼠的比较脑膜和潜在的化学计量关系。

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The levels of expression of Gsalpha(short and long), Galpha(olf) and Gbeta(common) subunits, and calcium-sensitive adenylyl cyclases isoforms (AC1, 5/6, and 8) in human brain cortical and caudate membranes were quantified by western blot analysis in order to establish their contribution to the patterns of AC functioning. Both areas expressed Gsalpha(long) (52 kDa) with values ranging from about 1400 ng/mg of membrane protein in cerebral cortex to close to 600 ng/mg of membrane protein in caudate nucleus. In contrast, Gsalpha(short) and Gsalpha(olf) were expressed separately, Gsalpha(short) in cortical membranes with values around 500 ng/mg of membrane protein and Galpha(olf) in caudate membranes with values around 1300 ng/mg of membrane protein. Quantitative measurements of Gbeta, revealed a similar expression level in cortical and caudate membranes (5444+/-732 versus 5511+/-394 ng/mg protein; p=0.966). The B(max) values of GTPgammaS-dependent [(3)H]-forskolin binding show the following descending order: rat striatal membranes>rat cortical membranes=human caudate membranes>human cortical membranes. Therefore, as measured immunochemically and by [(3)H]-forskolin binding, there seems to be a vast excess of Gsalpha subunits over catalytic units of AC. The highest levels of AC5/6 expression were detected in caudate membranes. AC8 was little expressed, and there were no significant differences in the relative values between both human brain regions. Finally, the levels of the AC1 isoform were significantly lower in caudate than in cortical membranes. It is concluded that these stoichiometric data contribute nonetheless to explain the significant differences observed in signalling capacities through the AC system in both human brain regions.
机译:Gsalpha(短和长),Galpha(olf)和Gbeta(常见)亚基以及钙敏感的腺苷酸环化酶同工型(AC1、5 / 6和8)在人大脑皮层和尾状膜中的表达水平通过免疫印迹分析是为了确定它们对AC功能模式的贡献。两个区域均表达Gsalpha(long)(52 kDa),其值范围从大脑皮层中的约1400 ng / mg的膜蛋白到尾状核中的接近600 ng / mg的膜蛋白。相反,Gsalpha(short)和Gsalpha(olf)分别表达,Gsalpha(short)在皮质膜中的表达约为500 ng / mg的膜蛋白,而Galpha(olf)在尾状膜中的表达约为1300 ng / mg的膜蛋白。 Gbeta的定量测量显示,在皮质和尾状膜中的表达水平相似(5444 +/- 732与5511 +/- 394 ng / mg蛋白; p = 0.966)。 GTPgammaS依赖性[(3)H]-福司柯林结合的B(max)值显示以下降序:大鼠纹状体膜>大鼠皮质膜=人尾状膜>人皮质膜。因此,如通过免疫化学方法和[[3)H]-佛司可林结合法测量的,Gsalpha亚基似乎比AC的催化单元大大过量。在尾状膜中检测到最高水平的AC5 / 6表达。 AC8很少表达,并且两个人脑区域之间的相对值没有显着差异。最后,尾状核中的AC1同工型水平显着低于皮质膜。结论是,这些化学计量数据仍然有助于解释在两个人脑区域中通过交流系统观察到的信号传递能力的显着差异。

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