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在体外共培养模型中,晶状体上皮支持视网膜神经节细胞的轴突再生。

Lens epithelium supports axonal regeneration of retinal ganglion cells in a coculture model in vitro.

作者信息

Stupp Tobias, Pavlidis Mitrofanis, Busse Holger, Thanos Solon

机构信息

Department of Experimental Ophthalmology, Interdisciplinary Research Centre (IZKF), School of Medicine, University Eye Hospital Münster, Domagkstr. 15, 48149 Münster, Germany.

出版信息

Exp Eye Res. 2005 Nov;81(5):530-8. doi: 10.1016/j.exer.2005.03.011. Epub 2005 Jul 19.

Abstract

The purpose of this study was to determine whether the lens epithelium influences the survival or axonal growth of regenerating retinal ganglion cells. The optic nerves of adult albino rats were injured in order to induce axonal regeneration, and axon growth was then studied in retinal explants in the presence of cocultivated lens capsules carrying living epithelial cells. In the first series of experiments, cocultivation of retinal explants with lens epithelium in immediate proximity resulted in penetration of fibers into the lens epithelium, indicating that it supported axonal growth. In the second series of experiments, co-explants were placed 0.5-1.0mm from each other. The numbers of outgrowing retinal axons were determined both with respect to the retinal eccentricity and the topological relationship with the lenticular co-explant. The Wilcoxon matched-pairs signed-rank test was used to determine if the numbers of axons differed significantly between four regions of the explants. Significantly more axons grew out from the retinal edge facing the lenticular explant than from its opposite side, indicating that the lens epithelium supports axon growth. The numbers of surviving retinal ganglion cells in culture were determined after retrograde prelabelling with a neuroanatomical tracer. The number of fluorescent ganglion cells within the retinal explants did not significantly differ between the groups (Mann-Whitney test). These findings indicate that the lens epithelium influences both the amount of axonal regeneration and the direction of growth without affecting the survival rate of retinal ganglion cells in vitro.

摘要

本研究的目的是确定晶状体上皮是否会影响再生视网膜神经节细胞的存活或轴突生长。为诱导轴突再生,成年白化大鼠的视神经受到损伤,然后在携带活上皮细胞的共培养晶状体囊存在的情况下,研究视网膜外植体中的轴突生长。在第一系列实验中,视网膜外植体与紧邻的晶状体上皮共培养导致纤维穿透到晶状体上皮中,表明其支持轴突生长。在第二系列实验中,共培养的外植体彼此相距0.5 - 1.0毫米。根据视网膜离心率以及与晶状体共培养外植体的拓扑关系,确定长出的视网膜轴突数量。采用Wilcoxon配对符号秩检验来确定外植体四个区域之间的轴突数量是否存在显著差异。从面向晶状体外植体的视网膜边缘长出的轴突明显多于其相对侧,表明晶状体上皮支持轴突生长。在用神经解剖学示踪剂进行逆行预标记后,确定培养物中存活的视网膜神经节细胞数量。视网膜外植体内的荧光神经节细胞数量在各组之间无显著差异(Mann - Whitney检验)。这些发现表明,晶状体上皮在体外既影响轴突再生的数量和生长方向,又不影响视网膜神经节细胞的存活率。

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