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白化兔视网膜中微胶质细胞的发育

Development of microglia in the albino rabbit retina.

作者信息

Ashwell K

机构信息

Department of Anatomy, University of Sydney, NSW, Australia.

出版信息

J Comp Neurol. 1989 Sep 15;287(3):286-301. doi: 10.1002/cne.902870303.

Abstract

In this study the development of ameboid microglia and resting microglia in the retina of the albino rabbit has been examined by means of a lectin derived from Griffonia simplicifolia. Ameboid microglia are present in the retina as early as E12, when the optic fissure is in the process of closure, and appear to be concentrated initially at the vitreal surface. At E14 many ameboid microglia can be seen to extend processes to the ventricular surface of the cytoblast layer, but in subsequent ages these cells are rare and ameboid microglia are largely confined to the ganglion cell layer, inner plexiform layer, and occasionally the developing inner nuclear layer. By adult life, mature (or resting) microglia are confined to the inner plexiform and ganglion cell layers. Numbers of microglia increase steadily throughout fetal life from a mean of 400 at E14, the earliest age quantified, to a peak of 28,600 at E30. There is a small postnatal drop in numbers to 17,150 at P9. Microglia could only be labelled faintly in animals older than P11, but analysis of two adult (P130) retinas with adequate labelling suggested that numbers rise to a value of about 23,800 at this age. Ameboid microglia thus appear in the retina 11 days prior to the onset of axon loss in the optic nerve (about E23) and 14 days prior to the beginning of the period of reduction of retinal ganglion cell numbers (about E26). The present findings indicate that while some microglial precursors may enter the retina in response to debris generated during the natural retinal ganglion cell death period, most enter the retina well before this period. Also, microglia present a uniform density distribution with apparently regular spacing as early as E16, so the uniform regular distribution cannot simply be the consequence of regularly distributed pyknotic figures as previously suggested.

摘要

在本研究中,利用一种源自西非相思豆的凝集素,对白化兔视网膜中阿米巴样小胶质细胞和静息小胶质细胞的发育进行了检测。早在胚胎第12天视裂闭合过程中,视网膜中就出现了阿米巴样小胶质细胞,最初似乎集中在玻璃体表面。在胚胎第14天,可以看到许多阿米巴样小胶质细胞伸出突起至成神经细胞层的室管膜表面,但在随后的发育阶段,这些细胞很少见,阿米巴样小胶质细胞主要局限于神经节细胞层、内网状层,偶尔也见于发育中的内核层。到成年时,成熟(或静息)小胶质细胞局限于内网状层和神经节细胞层。在整个胎儿期,小胶质细胞数量稳步增加,从最早量化的胚胎第14天的平均400个增加到胚胎第30天的峰值28,600个。出生后数量略有下降,在出生后第9天降至17,150个。在出生后11天以上的动物中,小胶质细胞只能被微弱标记,但对两个标记充分的成年(出生后第130天)视网膜的分析表明,这个年龄段小胶质细胞数量增加到约23,800个。因此,阿米巴样小胶质细胞在视神经轴突丧失开始前11天(约胚胎第23天)和视网膜神经节细胞数量减少期开始前14天(约胚胎第26天)出现在视网膜中。目前的研究结果表明,虽然一些小胶质细胞前体可能因自然视网膜神经节细胞死亡期产生的碎片而进入视网膜,但大多数在这个时期之前很久就进入了视网膜。此外,早在胚胎第16天,小胶质细胞就呈现出均匀的密度分布,间距明显规则,所以这种均匀规则的分布不可能简单地像之前所认为的那样是由规则分布的固缩核造成的。

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