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一只蝗虫中间神经元的胚胎期和胚后期形态发生

Embryonic and postembryonic morphogenesis of a grasshopper interneuron.

作者信息

Bentley D, Toroian-Raymond A

出版信息

J Comp Neurol. 1981 Oct 1;201(4):507-18. doi: 10.1002/cne.902010404.

DOI:10.1002/cne.902010404
PMID:7287932
Abstract

The object of this study was to describe the embryonic and postembryonic morphogenesis of a grasshopper interneuron in order to determine how, and when, this cell comes to assume its mature form. DCMD is an intensively investigated interneuron whose morphology, input and output physiology, and role in behavior are relatively well-known in the adult. We examined the morphology of DCMD in the brain at each stage of its development with silver-intensified cobalt-fills. It arises at 40 +/- 4% of embryogenesis and is probably one of the early progeny from its stem cell. In the ensuing 40% of development, its brain arborization grows quite directly into its mature form. Branches appear first and are always longest and densest in the brain region where the adult arborization is found. Thus, the adult form arises by initially directed growth and not by secondary selection of branches from a diffuse or overgrown arborization. Restricted secondary branch loss of lateral filopodia and probably of a few early branches does occur. Embryonic and postembryonic development of the cell are distinctly different. Embryogenesis is the period of morphological differentiation as indicated by the growth and shaping of the brain and also thoracic (axonal) arborizations, the appearance of cytological specializations, and the logarithmic growth of the neurite and soma. The brain arborization has its mature form, although not size, by the completion of embryogenesis. Postembryonic development is a period of substantial, but primarily allometric, growth. The soma and neurite grow linearly (with time), and the arborization grows in proportion to brain size.

摘要

本研究的目的是描述一种蝗虫中间神经元的胚胎期和胚后期形态发生,以确定该细胞如何以及何时形成其成熟形态。DCMD是一种经过深入研究的中间神经元,其形态、输入和输出生理学以及在成虫中的行为作用相对为人所知。我们用银强化钴填充法检查了DCMD在其发育各阶段大脑中的形态。它在胚胎发育的40±4%时出现,可能是其干细胞的早期后代之一。在随后40%的发育过程中,其在大脑中的分支结构直接生长为成熟形态。分支首先出现,并且在发现成虫分支结构的大脑区域总是最长且最密集。因此,成虫形态是通过最初的定向生长形成的,而不是通过从扩散或过度生长的分支结构中二次选择分支形成的。确实会发生侧生丝状伪足以及可能一些早期分支的有限二次分支丢失。该细胞的胚胎期和胚后期发育明显不同。胚胎发育是形态分化期,表现为大脑以及胸部(轴突)分支结构的生长和塑形、细胞学特化的出现以及神经突和胞体的对数生长。到胚胎发育完成时,大脑分支结构已具有成熟形态,尽管大小尚未达到成熟状态。胚后期发育是一个大量生长的时期,但主要是异速生长。胞体和神经突呈线性(随时间)生长,分支结构则与大脑大小成比例生长。

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