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甲状腺素向脑内的转运:脉络丛蛋白质合成的作用。

Thyroxine transport to the brain: role of protein synthesis by the choroid plexus.

作者信息

Southwell B R, Duan W, Alcorn D, Brack C, Richardson S J, Köhrle J, Schreiber G

机构信息

Russell Grimwade School of Biochemistry, University of Melbourne, Parkville, Victoria, Australia.

出版信息

Endocrinology. 1993 Nov;133(5):2116-26. doi: 10.1210/endo.133.5.8404661.

Abstract

A cell culture model for the blood-cerebrospinal fluid barrier in choroid plexus was developed. The relationship between synthesis and secretion of transthyretin across a layer of epithelial cells derived from rat choroid plexus and the transport of T4 was analyzed in a two-chamber system. Choroid plexus cells were dispersed and placed on a porous filter suspended in cell culture medium. A monolayer of polarized epithelial cells developed after 5 days in culture, separating fluid in the upper (apical) chamber from fluid in the lower (basal) chamber. Electrical resistance across the cell layer was 100 Ohm/cm2. Transthyretin was synthesized and secreted by these cells. Over 32 h, transthyretin accumulated in the fluid in the apical chamber to twice the concentration in the basal chamber. [125I]T4 added to the basal chamber permeated to the apical fluid and accumulated in the apical chamber to twice the concentration in the basal fluid. Upon inhibition of protein synthesis, T4 equilibrated to a similar concentration in the two chambers. Thus, the accumulation of T4 in the apical chamber required continuing protein synthesis. Competitive inhibition of T4 binding to transthyretin by EMD 21388 also prevented the accumulation of T4 to a higher concentration in the upper than in the lower chamber. These data suggest that T4 partitions through the choroid plexus and that transthyretin synthesis and secretion by the choroid plexus determines the concentration of T4 in the apical fluid. A model is proposed for the involvement of transthyretin secreted by the choroid plexus, in the in vivo distribution of T4 in the brain.

摘要

建立了脉络丛血脑屏障的细胞培养模型。在双室系统中分析了转甲状腺素蛋白在源自大鼠脉络丛的一层上皮细胞中的合成与分泌以及T4的转运之间的关系。将脉络丛细胞分散并置于悬浮在细胞培养基中的多孔滤膜上。培养5天后形成了一层极化上皮细胞单层,将上室(顶端)的液体与下室(基底)的液体分隔开。跨细胞层的电阻为100欧姆/平方厘米。这些细胞合成并分泌转甲状腺素蛋白。在32小时内,转甲状腺素蛋白在顶端室的液体中积累,其浓度是基底室的两倍。添加到基底室的[125I]T4渗透到顶端液体中,并在顶端室中积累,其浓度是基底液体的两倍。抑制蛋白质合成后,T4在两个室中的浓度达到平衡。因此,T4在顶端室中的积累需要持续的蛋白质合成。EMD 21388对T4与转甲状腺素蛋白结合的竞争性抑制也阻止了T4在顶端室中积累到比基底室更高的浓度。这些数据表明,T4通过脉络丛进行分配,脉络丛合成和分泌转甲状腺素蛋白决定了顶端液体中T4的浓度。提出了一个关于脉络丛分泌的转甲状腺素蛋白参与T4在脑内体内分布的模型。

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