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遗传性视神经发育不全小鼠眼部的发育与老化:组织病理学研究

Development and aging of the eye in mice with inherited optic nerve aplasia: histopathological studies.

作者信息

Silver J, Puck S M, Albert D M

出版信息

Exp Eye Res. 1984 Mar;38(3):257-66. doi: 10.1016/0014-4835(84)90164-7.

Abstract

We have examined the morphological development of optic nerve aplasia in a subpopulation (10-20%) of anophthalmic mice (Strain ZRDCT -AN) that develop microphthalmia. During embryonic stages the optic fissure in microphthalmic mutants did not involute into the optic stalk. Even in the absence of a proper fissure, early differentiation of the various retinal elements was not disturbed. Subsequently, however, the optic nerve fibers failed to exit from the eye in their appropriate position. Secondary changes in the retina, probably resulting from a failure of optic axons to reach their central targets, were near total loss of ganglion cells and variable attenuation of the other nuclear and plexiform layers. Retinal rosettes were also commonly present.

摘要

我们研究了患有小眼症的无眼小鼠(ZRDCT-AN品系)亚群(10%-20%)中视神经发育不全的形态学发展。在胚胎阶段,小眼症突变体中的视裂未卷入视神经柄。即使没有适当的视裂,各种视网膜成分的早期分化也未受干扰。然而,随后视神经纤维未能在其适当位置从眼中穿出。视网膜的继发性变化,可能是由于视神经轴突未能到达其中枢靶点所致,表现为神经节细胞几乎完全丧失,以及其他核层和神经丛层不同程度的变薄。视网膜玫瑰花结也普遍存在。

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