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大鼠脑中钙结合蛋白D-28k的蛋白质与mRNA定位

Calbindin D-28k Protein and mRNA Localization in the Rat Brain.

作者信息

Séquier J. M., Hunziker W., Andressen C., Celio M. R.

机构信息

Central and Pharmaceutical Research Department, F. Hoffmann-La Roche and Co. Ltd, CH-4002 Basle, Switzerland.

出版信息

Eur J Neurosci. 1990;2(12):1118-1126. doi: 10.1111/j.1460-9568.1990.tb00023.x.

Abstract

After the discovery of calretinin, a protein with high sequence homology to calbindin D-28k, the validity of immunohistochemical results obtained using polyclonal antibodies for this protein, was in question. In order to validate the previous results on the localization of calbindin D-28k in the brain, we localized the protein by highly specific monoclonal antibodies and revealed its mRNA histochemically by in situ hybridization. In general there was good agreement between the results obtained using these two different techniques and those reported in previous publications. The concordance was particularly impressive for the cerebral cortex, basal ganglia, basal nucleus of Meynert, hippocampus, thalamus, cerebellum and superior colliculus. In the amygdala and hypothalamus the low spatial resolution of in situ hybridization did not allow precise definition of some nuclei displaying a positive reaction for the protein. In the rhombencephalon, cells of the parabrachial nuclei and the dorsal raphe nucleus expressed calbindin D-28k. Neurons in the dorsal horn of the spinal cord and some horizontal cells of the retina were tagged with both methods. The only discrepancy was the presence of immunoreactive ependymal cells, whereas mRNA never occurred in cells lining the ventricles. Thus, the combined approach has established the widespread distribution of cells expressing calbindin D-28k in the rat brain.

摘要

在发现钙结合蛋白D - 28k的一种与钙视网膜蛋白具有高度序列同源性的蛋白质后,使用针对该蛋白质的多克隆抗体获得的免疫组织化学结果的有效性受到质疑。为了验证先前关于钙结合蛋白D - 28k在脑中定位的结果,我们用高度特异性的单克隆抗体对该蛋白质进行定位,并通过原位杂交对其mRNA进行组织化学显示。总体而言,使用这两种不同技术获得的结果与先前出版物中报道的结果之间有很好的一致性。对于大脑皮层、基底神经节、迈内特基底核、海马体、丘脑、小脑和上丘,这种一致性尤其令人印象深刻。在杏仁核和下丘脑,原位杂交的低空间分辨率不允许精确界定一些对该蛋白质呈阳性反应的核。在菱脑,臂旁核和中缝背核的细胞表达钙结合蛋白D - 28k。脊髓背角的神经元和视网膜的一些水平细胞用这两种方法都被标记。唯一的差异是存在免疫反应性室管膜细胞,而mRNA从未出现在脑室衬里细胞中。因此,联合方法确定了大鼠脑中表达钙结合蛋白D - 28k的细胞的广泛分布。

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