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通过放射自显影定位在预变态五龄烟草天蛾幼虫中枢神经系统中的蜕皮甾体结合位点。

Ecdysteroid binding sites localized by autoradiography in the central nervous system of precommitment fifth-stadium Manduca sexta larvae.

作者信息

Bidmon H J, Stumpf W E, Granger N A

机构信息

Department of Cell Biology and Anatomy, University of North Carolina, Chapel Hill 27599-7090.

出版信息

Cell Tissue Res. 1991 Jan;263(1):183-94. doi: 10.1007/BF00318414.

DOI:10.1007/BF00318414
PMID:2009550
Abstract

Brains and subesophageal ganglia from day 3.5 fifth stadium larvae of Manduca sexta were incubated in vitro with 4 nM tritiated ponasterone A, a 20-hydroxyecdysone analog, to determine whether uptake and specific binding of ecdysteroids occur at a cellular level. These tissues, which were taken just prior to the commitment peak in the hemolymph-ecdysteroid titer, showed saturable uptake of 3H-ponasterone A after 40-60 min of incubation. Uptake was blocked by the addition of 400 nM unlabelled ponasterone A, or of 500 nM or 1000 nM 20-hydroxyecdysone. RH 5849, a synthetic 20-hydroxyecdysone agonist with a long half-life, for which ecdysteroid receptors have low affinity, also reduced ponasterone A uptake at a concentration of 10 microM. Autoradiographs of 4 microns sections of brains revealed distinct nuclear concentrations of silver grains over cell populations in the pars intercerebralis, pars lateralis, and ventral tritocerebrum. Nuclear labelling was also found in many small cells around the mushroom bodies and the neuropil, and between the inner and outer larval optic lobes. Nuclear labelling of cells in the subesophageal ganglion was observed in the fronto-medial and lateral regions, in small cells around the neuropil, and caudally in a few large neurons. In addition to cells with nuclear labelling, both brains and ganglia at this development stage contained cells with exclusively cytoplasmic or both nuclear and cytoplasmic labelling. None of these apparent binding sites were observed in the competition experiments, suggesting that the binding is specific.

摘要

将烟草天蛾五龄幼虫第3.5天的脑和咽下神经节与4 nM氚标记的蜕皮甾酮A(一种20-羟基蜕皮激素类似物)进行体外孵育,以确定蜕皮甾类的摄取和特异性结合是否发生在细胞水平。这些组织是在血淋巴蜕皮甾类滴度达到峰值之前采集的,孵育40 - 60分钟后,显示出对3H-蜕皮甾酮A的饱和摄取。加入400 nM未标记的蜕皮甾酮A、500 nM或1000 nM 20-羟基蜕皮激素可阻断摄取。RH 5849是一种具有长半衰期的合成20-羟基蜕皮激素激动剂,蜕皮甾类受体对其亲和力较低,在浓度为10 microM时也能降低蜕皮甾酮A的摄取。对4微米厚的脑切片进行放射自显影,结果显示在脑间部、外侧部和腹侧后脑的细胞群上有明显的银颗粒核内聚集。在蘑菇体和神经纤维周围的许多小细胞中,以及幼虫内、外视叶之间也发现了核标记。在咽下神经节中,额内侧和外侧区域、神经纤维周围的小细胞以及尾部少数大神经元中观察到细胞的核标记。除了有核标记的细胞外,处于这个发育阶段的脑和神经节中还含有仅具有胞质标记或同时具有核标记和胞质标记的细胞。在竞争实验中未观察到这些明显的结合位点,这表明这种结合是特异性的。

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本文引用的文献

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