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利用在人类细胞中表达的生物发光水母发光蛋白测量细胞内钙含量。

Measurement of intracellular calcium using bioluminescent aequorin expressed in human cells.

作者信息

Sheu Y A, Kricka L J, Pritchett D B

机构信息

Department of Pharmacology, University of Pennsylvania School of Medicine, Philadelphia.

出版信息

Anal Biochem. 1993 Mar;209(2):343-7. doi: 10.1006/abio.1993.1132.

Abstract

Changes in intracellular free calcium concentration ([Ca2+]i) are involved in many important physiological responses. Detecting changes in [Ca2+]i is crucial to understanding the physiologic roles of intracellular free calcium. We have characterized changes of [Ca2+]i in human cells transfected with apoaequorin cDNA. When reconstituted in vivo by incubating transfected cells with coelenterazine, aequorin emits light upon binding free calcium and acts as a bioluminescent indicator for calcium. We have used this system to determine the concentration response relationship of serotonin for its receptor. Cells cotransfected with serotonin receptor cDNA and apoaequorin cDNA emitted light upon treatment with serotonin. The light emission responses were saturable and serotonin concentration-dependent, and they were inhibited by serotonin antagonists. Human 293 cells that stably express apoaequorin have been created. This system should facilitate the investigation of [Ca2+]i involvement in physiological and pathophysiological responses.

摘要

细胞内游离钙浓度([Ca2+]i)的变化参与许多重要的生理反应。检测[Ca2+]i的变化对于理解细胞内游离钙的生理作用至关重要。我们已经对转染了脱辅基水母发光蛋白cDNA的人类细胞中[Ca2+]i的变化进行了表征。当通过用腔肠素孵育转染细胞在体内进行重组时,水母发光蛋白在结合游离钙时会发光,并作为钙的生物发光指示剂。我们已经使用这个系统来确定血清素与其受体的浓度反应关系。用血清素处理后,共转染血清素受体cDNA和脱辅基水母发光蛋白cDNA的细胞会发光。发光反应是可饱和的且依赖于血清素浓度,并且它们被血清素拮抗剂抑制。已经创建了稳定表达脱辅基水母发光蛋白的人类293细胞。该系统应有助于研究[Ca2+]i参与生理和病理生理反应的情况。

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