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类固醇激素、树突重塑与神经元死亡:来自昆虫变态发育的见解

Steroid hormones, dendritic remodeling and neuronal death: insights from insect metamorphosis.

作者信息

Weeks J C

机构信息

Institute of Neuroscience, University of Oregon, Eugene 97403-1254, USA.

出版信息

Brain Behav Evol. 1999;54(1):51-60. doi: 10.1159/000006611.

Abstract

Steroid hormones influence neuronal structure and function throughout the animal kingdom, via highly conserved receptor proteins. Insights into steroid effects on neurons and behavior have come from a range of vertebrate species including reptiles, amphibians, fish, birds, rodents and primates. In many instances, steroid hormones regulate the volume of particular regions of the nervous system by affecting both the number of constituent neurons and their size. A major determinant of neuronal number is the process of programmed cell death (PCD), which involves molecular machinery that is conserved across species. This article reviews steroid-mediated PCD and dendritic remodeling during metamorphosis of the hawkmoth, Manduca sexta. Metamorphosis is driven by a class of steroid hormones, the ecdysteroids. During the transformation from larva to pupa to adult moth, accessory planta retractor (APR) motoneurons of Manduca undergo dendritic regression and regrowth, and segment-specific PCD, in response to specific ecdysteroid cues. Experiments utilizing APRs in primary cell culture show that PCD is a direct response to ecdysteroids, regulated by the intrinsic segmental identity of individual APRs. As in other systems, activation of caspases (cysteine proteases) is involved in the execution phase of PCD. Other experiments demonstrate that the ecdysteroid-mediated regression of APRs' dendrites at pupation causes weakening of monosynaptic excitatory inputs from sensory neurons that trigger a larval withdrawal reflex. Thus, the steroid-mediated reduction in dendritic extent is linked to a specific electrophysiological and behavioral change during metamorphosis. The comparative approach, taking advantage of a variety of vertebrate and invertebrate species, holds the most promise for elucidating the full spectrum of steroid effects on neurons and behavior.

摘要

类固醇激素通过高度保守的受体蛋白影响整个动物界的神经元结构和功能。对类固醇对神经元和行为影响的深入了解来自一系列脊椎动物物种,包括爬行动物、两栖动物、鱼类、鸟类、啮齿动物和灵长类动物。在许多情况下,类固醇激素通过影响组成神经元的数量及其大小来调节神经系统特定区域的体积。神经元数量的一个主要决定因素是程序性细胞死亡(PCD)过程,该过程涉及跨物种保守的分子机制。本文综述了烟草天蛾变态过程中类固醇介导的PCD和树突重塑。变态由一类类固醇激素蜕皮类固醇驱动。在从幼虫到蛹再到成虫蛾的转变过程中,烟草天蛾的副植物牵缩肌(APR)运动神经元会响应特定的蜕皮类固醇信号,经历树突退缩和再生以及特定节段的PCD。在原代细胞培养中利用APR进行的实验表明,PCD是对蜕皮类固醇的直接反应,受单个APR的内在节段身份调节。与其他系统一样,半胱天冬酶(半胱氨酸蛋白酶)的激活参与了PCD的执行阶段。其他实验表明,蜕皮类固醇介导的化蛹时APR树突退缩会导致触发幼虫退缩反射的感觉神经元的单突触兴奋性输入减弱。因此,类固醇介导的树突范围减少与变态过程中特定的电生理和行为变化有关。利用各种脊椎动物和无脊椎动物物种的比较方法,最有希望阐明类固醇对神经元和行为影响的全貌。

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