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20-羟基蜕皮激素对黑腹果蝇眼成虫盘细胞体外分化的影响。

The effects of 20-hydroxyecdysone on the differentiation in vitro of cells from the eye imaginal disc from Drosophila melanogaster.

作者信息

Li C, Meinertzhagen I A

机构信息

Neuroscience Institute, Dalhousie University, Halifax, Nova Scotia, Canada.

出版信息

Invert Neurosci. 1997 Jun;3(1):57-69. doi: 10.1007/BF02481715.

Abstract

We have examined the effects of the insect ecdysteroid, 20-hydroxyecdysone, on the differentiation of neuronal and non-neuronal elements in the developing adult visual system, using in vitro methods in Drosophila. We examined the differentiation of early neuronal markers in the presence and absence of 1 microgram/ml 20-hydroxyecdysone. Immunoreactivity to 22C10, a marker of an early neuronal antigen, as well as to the photoreceptor-specific antibody 24B10, suggests that differentiation of neuronal and photoreceptor antigens does not require 20-hydroxyecdysone. In eye-discs cultured from animals 5 hours after the white prepupa (P + 5), ommochrome pigmentation first appeared after 2 days in 1 microgram/ml 20-hydroxyecdysone, but cultures lacked pigmentation without 20-hydroxyecdysone. Our culture conditions failed to support the formation of the second screening pigment, drosopterins, even with 20-hydroxyecdysone. Eye discs from P + 5 also formed lenses and interommatidial bristles in culture when 20-hydroxyecdysone was added but not in cultures devoid of the hormone. The differentiation of synaptotagmin and the elongation of extending photoreceptor neurites from eye disc fragments both occur in the absence of 20-hydroxyecdysone in cultures, but adding the hormone increased average neurite length. The threshold for enhanced neurite length was less than 125 ng/ml 20-hydroxyecdysone. Eye-disc cultures also developed immunoreactivity to histamine, the photoreceptor transmitter, from synthesis not re-uptake, in both the presence and in the absence of 20-hydroxyecdysone. These findings suggest that photoreceptor axons may be able to release transmitter in vivo both when they grow into the optic lobe and during the subsequent events in synapse formation.

摘要

我们运用果蝇体外培养方法,研究了昆虫蜕皮甾体20-羟基蜕皮酮对成年视觉系统发育过程中神经元和非神经元成分分化的影响。我们检测了在存在和不存在1微克/毫升20-羟基蜕皮酮的情况下早期神经元标记物的分化情况。针对早期神经元抗原标记物22C10以及光感受器特异性抗体24B10的免疫反应表明,神经元和光感受器抗原的分化并不需要20-羟基蜕皮酮。在白色蛹期后5小时(P + 5)的动物培养的眼盘中,1微克/毫升20-羟基蜕皮酮处理2天后首次出现眼色素沉着,但无20-羟基蜕皮酮时培养物无色素沉着。即使添加20-羟基蜕皮酮,我们的培养条件也无法支持第二种筛选色素即果蝇蝶呤的形成。当添加20-羟基蜕皮酮时,P + 5期的眼盘在培养中也能形成晶状体和小眼间刚毛,而在无该激素的培养物中则不能。在培养物中,即使没有20-羟基蜕皮酮,突触结合蛋白的分化以及眼盘片段中延伸的光感受器神经突的伸长也会发生,但添加该激素会增加神经突的平均长度。增强神经突长度的阈值低于125纳克/毫升20-羟基蜕皮酮。在存在和不存在20-羟基蜕皮酮的情况下,眼盘培养物均从合成而非再摄取中产生对光感受器递质组胺的免疫反应。这些发现表明,光感受器轴突在向视叶生长以及随后的突触形成过程中,在体内可能都能够释放递质。

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