Suppr超能文献

BW大鼠的复杂性缺损性小眼症:一种遗传性视网膜变性的新形式。

Complicated colobomatous microphthalmos in the BW rat: a new form of inherited retinal degeneration.

作者信息

Wyse J P, Hollenberg M J

出版信息

Am J Anat. 1977 Jul;149(3):377-411. doi: 10.1002/aja.1001490305.

Abstract

A new model of inherited retinal degeneration has been found in the rat. It is inherited in association with a number of other ocular defects, including microphthalmos, coloboma, retinal dysplasia, optic nerve hypoplasia and/or aplasia, as well as medullation of the nerve fiber layer of the retina. Together, these abnormalities constitute a condition referred to as complicated colobomatous microphthalmos. This condition was originally discovered in the Bmn strain of rats but subsequently transferred to a new genetic background in the Bmn-wys strain of rats (BW). This facilitated the histological evaluation of both the developmental and degenerative ocular defects in the adult animals. A well defined pattern emerged relating eye size, optic nerve size and retinal histology. Normal-sized eyes had normal-sized optic nerves and normal retinal histology while intermediate-sized eyes with no optic nerves had uniformly thin retinas. In contrast, intermediate-sized eyes with small optic nerves had areas of both normal thickness and thin retina. All of these eyes developed retinal degeneration characterized by a late onset and slow progression associated with normal phagocytic activity in the pigment epithelium and a tendency for the rod outer segments to fragment into very thin structures rather than accumulate as lamellar debris. This indicates that the retinal degeneration in the BW model differs in many respects from the well studied RCS model.

摘要

在大鼠中发现了一种遗传性视网膜变性的新模型。它与许多其他眼部缺陷相关遗传,包括小眼症、缺损、视网膜发育异常、视神经发育不全和/或发育不全,以及视网膜神经纤维层的髓鞘形成。这些异常共同构成了一种称为复杂性缺损性小眼症的病症。这种病症最初在大鼠的Bmn品系中发现,但随后转移到大鼠的Bmn-wys品系(BW)的新遗传背景中。这有助于对成年动物发育性和退行性眼部缺陷进行组织学评估。出现了一种明确的模式,涉及眼睛大小、视神经大小和视网膜组织学。正常大小的眼睛有正常大小的视神经和正常的视网膜组织学,而没有视神经的中等大小的眼睛视网膜均匀变薄。相比之下,有小视神经的中等大小的眼睛既有正常厚度的区域,也有薄视网膜区域。所有这些眼睛都发生了视网膜变性,其特征是发病晚、进展缓慢,色素上皮细胞吞噬活性正常,视杆细胞外段倾向于分裂成非常薄的结构,而不是堆积成层状碎片。这表明BW模型中的视网膜变性在许多方面与研究充分的RCS模型不同。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验