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人类视网膜中的D2多巴胺受体:cDNA的克隆与mRNA的定位

D2 dopamine receptors in the human retina: cloning of cDNA and localization of mRNA.

作者信息

Dearry A, Falardeau P, Shores C, Caron M G

机构信息

Department of Cell Biology, Duke University Medical Center, Durham, North Carolina 27710.

出版信息

Cell Mol Neurobiol. 1991 Oct;11(5):437-53. doi: 10.1007/BF00734808.

Abstract
  1. We have obtained a cDNA clone encoding a human retinal D2 dopamine receptor. 2. The longest open reading frame (1242 bp) of this clone encodes a protein of 414 amino acids having a predicted molecular weight of 47,000 and a transmembrane topology similar to that of other G protein-coupled receptors. 3. Transient transfection of COS-7 cells with an expression vector containing the clone resulted in expression of a protein possessing a pharmacological profile similar to that of the D2 dopamine receptor found in striatum and retina. 4. Northern blot analysis indicated that, in rat brain and retina, the mRNA for this receptor was 2.9 kb in size. 5. In situ hybridization was performed to examine the distribution of the mRNA for this receptor in human retina. Specific hybridization was detected in both the inner and the outer nuclear layers. 6. These findings are consistent with prior physiological and autoradiographic studies describing the localization of D2 dopamine receptors in vertebrate retinas. Our observations suggest that photoreceptors as well as cells in the inner nuclear layer of human retinas may express the mRNA for this D2 dopamine receptor.
摘要
  1. 我们获得了一个编码人视网膜D2多巴胺受体的cDNA克隆。2. 该克隆最长的开放阅读框(1242bp)编码一个414个氨基酸的蛋白质,预测分子量为47000,其跨膜拓扑结构与其他G蛋白偶联受体相似。3. 用含有该克隆的表达载体瞬时转染COS-7细胞,导致表达出一种蛋白质,其药理学特性与在纹状体和视网膜中发现的D2多巴胺受体相似。4. Northern印迹分析表明,在大鼠脑和视网膜中,该受体的mRNA大小为2.9kb。5. 进行原位杂交以检测该受体的mRNA在人视网膜中的分布。在内核层和外核层均检测到特异性杂交信号。6. 这些发现与先前描述脊椎动物视网膜中D2多巴胺受体定位的生理学和放射自显影研究一致。我们的观察结果表明,人视网膜的光感受器以及内核层中的细胞可能表达这种D2多巴胺受体的mRNA。

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本文引用的文献

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Neurotransmitter-related features of the retinal pigment epithelium.
Neurochem Int. 1983;5(3):285-90. doi: 10.1016/0197-0186(83)90030-x.
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J Comp Neurol. 1982 Sep 1;210(1):65-79. doi: 10.1002/cne.902100108.
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