首页> 美国卫生研究院文献>Proceedings of the National Academy of Sciences of the United States of America >Chinese hamster ovary cell population density affects intracellular concentrations of calcium-dependent regulator and ability of regulator to inhibit adenylate cyclase activity
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Chinese hamster ovary cell population density affects intracellular concentrations of calcium-dependent regulator and ability of regulator to inhibit adenylate cyclase activity

机译:中国仓鼠卵巢细胞群密度影响细胞内钙依赖性调节剂的浓度和调节剂抑制腺苷酸环化酶活性的能力

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摘要

The adenylate cyclase activity [ATP pyrophosphate-lyase (cyclizing), EC 4.6.1.1] of crude Chinese hamster ovary cell membranes was inhibited 30-40% by low concentrations (6-600 ng/ml) of calcium-dependent regulator (CDR). This inhibitory effect was lost at concentrations of CDR above 600 ng/ml. The adenylate cyclase activity of membranes prepared from low population density Chinese hamster ovary cells was not appreciably altered by CDR. However, with increasing cell population density there was a significant increase in the ability of CDR to inhibit cyclic AMP formation. Further, the intracellular levels of CDR determined in the 12,000 × g supernatant and particulate fractions varied inversely with increasing cell population density. As cell number increased from 2 × 106 to 10 × 106 cells per dish the CDR concentration present in the supernatant fraction increased from 0.4 to 0.8 μg of CDR per mg of protein, while the amount of endogenous CDR associated with the particulate fraction decreased from 0.6 to 0.4 μg of CDR per mg of protein. This suggests that possible changes in the distribution of CDR between the supernatant and membrane fractions might serve as a regulatory mechanism for activities under CDR control.
机译:中国仓鼠卵巢细胞膜的腺苷酸环化酶活性[ATP焦磷酸裂解酶(环化),EC 4.6.1.1]被低浓度(6-600 ng / ml)的钙依赖性调节剂(CDR)抑制了30-40%。 。当CDR浓度超过600 ng / ml时,这种抑制作用消失了。由低种群密度中国仓鼠卵巢细胞制备的膜的腺苷酸环化酶活性没有被CDR明显改变。但是,随着细胞种群密度的增加,CDR抑制环状AMP形成的能力显着增加。此外,在12,000×g上清液和颗粒级分中测定的CDR的细胞内水平随细胞群体密度的增加成反比。随着每个培养皿中细胞数从2×10 6 增加到10×10 6 细胞,上清液组分中存在的CDR浓度从0.4 mg / g到0.8μgCDR / mg蛋白质,而与微粒级分相关的内源性CDR的量则从每mg蛋白质0.6到0.4μgCDR减少。这表明上清液和膜级分之间CDR分布的可能变化可能是CDR控制下活性的调节机制。

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