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促甲状腺激素对猪甲状腺单层细胞中甲状腺球蛋白顶端和基底外排的调节作用。

Thyrotrophin regulation of apical and basal exocytosis of thyroglobulin by porcine thyroid monolayers.

作者信息

Chambard M, Depetris D, Gruffat D, Gonzalvez S, Mauchamp J, Chabaud O

机构信息

INSERM Unité 270, Faculté de Médecine Nord, Marseille, France.

出版信息

J Mol Endocrinol. 1990 Jun;4(3):193-9. doi: 10.1677/jme.0.0040193.

Abstract

Exocytosis, the ultimate step in thyroglobulin secretion, has been studied in porcine thyroid cells cultured in monolayers on the permeable bottom of culture chambers. We have previously demonstrated, using this culture system, that apical secretion accounts for 85-95% of total secretion of newly synthesized thyroglobulin. When cells were cultured for several days with bovine TSH (25 microU/ml) in the basal medium, the rate of glycoprotein accumulation in the upper compartment was three times higher than that in the absence of TSH. In contrast, the rate of thyroglobulin released into the basal medium (5-15% of total secreted thyroglobulin) appeared unmodified by chronic TSH stimulation. To investigate the effect of acute TSH stimulation on thyroglobulin exocytosis in the apical and basal compartments, pulse-chase experiments were carried out with the same culture system. The release of radiolabelled thyroglobulin (1.5-h pulse) into the apical medium was increased threefold during the 2-h chase period under TSH stimulation. The radiolabelled thyroglobulin released into the basal medium was increased only 1.5- to 2-fold, and stimulation disappeared after 1 h. The effect of TSH was maximal when the chase medium contained 50 microU TSH/ml. However, cells cultured for several days in the presence of 25 microU TSH/ml before the pulse-chase experiment, appeared desensitized to acute TSH stimulation. Similar responses were observed when the chase medium contained 8-chloro-cyclic AMP or cholera toxin. This study provides another example of the pleiotropic effect of TSH, mediated by cyclic AMP, on the sequential steps of thyroglobulin gene expression in cultured thyroid cells in which the polar character of the epithelial cells is well preserved.

摘要

胞吐作用是甲状腺球蛋白分泌的最终步骤,我们在培养于培养室可渗透底部的单层猪甲状腺细胞中对其进行了研究。我们之前使用该培养系统证明,顶端分泌占新合成甲状腺球蛋白总分泌量的85%-95%。当细胞在基础培养基中用牛促甲状腺激素(25微单位/毫升)培养数天时,上室中糖蛋白的积累速率比无促甲状腺激素时高3倍。相比之下,释放到基础培养基中的甲状腺球蛋白速率(占分泌的甲状腺球蛋白总量的5%-15%)似乎不受慢性促甲状腺激素刺激的影响。为了研究急性促甲状腺激素刺激对顶端和基础隔室中甲状腺球蛋白胞吐作用的影响,我们使用相同的培养系统进行了脉冲追踪实验。在促甲状腺激素刺激下的2小时追踪期内,释放到顶端培养基中的放射性标记甲状腺球蛋白(1.5小时脉冲)增加了3倍。释放到基础培养基中的放射性标记甲状腺球蛋白仅增加了1.5至2倍,且刺激在1小时后消失。当追踪培养基中含有50微单位促甲状腺激素/毫升时,促甲状腺激素的作用最大。然而,在脉冲追踪实验前在含有25微单位促甲状腺激素/毫升的条件下培养数天的细胞,似乎对急性促甲状腺激素刺激不敏感。当追踪培养基中含有8-氯环磷酸腺苷或霍乱毒素时,观察到了类似的反应。本研究提供了另一个例子,说明促甲状腺激素通过环磷酸腺苷介导的多效性作用,对培养的甲状腺细胞中甲状腺球蛋白基因表达的连续步骤产生影响,其中上皮细胞的极性特征得到了很好的保留。

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