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大鼠神经系统中易化尿素转运体UT3的mRNA分布

Distribution of mRNA for the facilitated urea transporter UT3 in the rat nervous system.

作者信息

Berger U V, Tsukaguchi H, Hediger M A

机构信息

Department of Medicine, Brigham and Women's Hospital, Harvard Medical School, Harvard Institutes of Medicine, Boston, MA 02115, USA.

出版信息

Anat Embryol (Berl). 1998 May;197(5):405-14. doi: 10.1007/s004290050152.

Abstract

Recently, the cDNA encoding the rat urea transporter UT3 has been cloned from rat kidney. Here we describe the cellular localization of this transporter in the brain as detected by non-radioactive in situ hybridization. UT3 is expressed in astrocytes throughout the central nervous system as well as in Bergmann glia in the cerebellum. The expression in astrocytes was verified by double staining using the astrocytic marker GFAP. UT3 mRNA is also strongly expressed by the ependymal cells lining the cerebral ventricles and by Müller cells in the retina. Furthermore, UT3 expression was detected in subgroups of neurons in the inferior colliculus and dorsal root ganglia, as well as in cells in the anterior pituitary gland. Other types of brain cells, including oligodendrocytes, microglia, tanycytes, endothelial cells of blood vessels, and epithelial cells in the choroid plexus were devoid of UT3 mRNA. Northern blot analysis confirmed that the mRNA species in the brain and in dorsal root ganglia are identical, and that cultured astrocytes and C6 cells also express the UT3 mRNA. UT3 mRNA expression by astrocytes is markedly upregulated in quinolinic acid-induced gliosis, possibly as a result of increased urea levels during gliosis induced polyamine formation. We propose that UT3 in astrocytes represents a mechanism to control urea formed in the brain by equilibrating it throughout the astrocyte network and guiding it to blood vessels and the CSF for disposal.

摘要

最近,编码大鼠尿素转运体UT3的cDNA已从大鼠肾脏中克隆出来。在此,我们描述了通过非放射性原位杂交检测到的该转运体在大脑中的细胞定位。UT3在整个中枢神经系统的星形胶质细胞以及小脑中的伯格曼胶质细胞中表达。使用星形胶质细胞标志物GFAP进行双重染色证实了UT3在星形胶质细胞中的表达。UT3 mRNA在脑室衬里的室管膜细胞和视网膜中的穆勒细胞中也强烈表达。此外,在下丘和背根神经节的神经元亚群以及垂体前叶细胞中检测到了UT3的表达。其他类型的脑细胞,包括少突胶质细胞、小胶质细胞、伸长细胞、血管内皮细胞和脉络丛中的上皮细胞均未检测到UT3 mRNA。Northern印迹分析证实大脑和背根神经节中的mRNA种类相同,并且培养的星形胶质细胞和C6细胞也表达UT3 mRNA。在喹啉酸诱导的胶质增生中,星形胶质细胞的UT3 mRNA表达明显上调,这可能是由于胶质增生诱导多胺形成过程中尿素水平升高所致。我们提出,星形胶质细胞中的UT3代表了一种机制,通过在整个星形胶质细胞网络中平衡尿素并将其导向血管和脑脊液进行处理,从而控制大脑中形成的尿素。

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