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硫酸软骨素蛋白聚糖可能会影响视网膜神经节细胞轴突生长的方向。

A chondroitin sulfate proteoglycan may influence the direction of retinal ganglion cell outgrowth.

作者信息

Snow D M, Watanabe M, Letourneau P C, Silver J

机构信息

University of Minnesota, Department of Cell Biology and Neuroanatomy, Minneapolis.

出版信息

Development. 1991 Dec;113(4):1473-85. doi: 10.1242/dev.113.4.1473.

Abstract

In the developing retina, retinal ganglion cell (RGC) axons elongate toward the optic fissure, even though no obvious directional restrictions exist. Previous studies indicate that axon-matrix interactions are important for retinal ganglion cell axon elongation, but the factors that direct elongation are unknown. Chondroitin sulfate proteoglycan (CS-PG), a component of the extracellular matrix, repels elongating dorsal root ganglion (DRG) axons in vitro and is present in vivo in the roof plate of the spinal cord, a structure that acts as a barrier to DRG axons during development. In this study, we examined whether CS-PG may regulate the pattern of retinal ganglion cell outgrowth in the developing retina. Immunocytochemical analysis showed that CS-PG was present in the innermost layers of the developing rat retina. The expression of CS-PG moved peripherally with retinal development, always remaining at the outer edge of the front of the developing axons. CS-PG was no longer detectable with immunocytochemical techniques when RGC axon elongation in the retina is complete. Results of studies in vitro showed that CS-PG, isolated from bovine nasal cartilage and chick limb, was inhibitory to elongating RGC axons and that RGC growth cones were more sensitive to CS-PG than were DRG neurites tested at the same concentrations of CS-PG. The behavior of retinal growth cones as they encounter CS-PG was characterized using time-lapse video microscopy. Filopodia of the RGC growth cones extended to and sampled the CS-PG repeatedly. With time, the growth cones turned to avoid outgrowth on the CS-PG and grew only on laminin. While numerous studies have shown the presence of positive factors within the retina that may guide developing RGC axons, this is the first demonstration of an inhibitory or repelling molecule in the retina that may regulate axon elongation. Taken together, these data suggest that the direction of RGC outgrowth in the retina may be regulated by the proper ratio of growth-promoting molecules, such as laminin, to growth-inhibiting molecules, like CS-PG, present in the correct pattern and concentrations along the retinal ganglion cell pathway.

摘要

在发育中的视网膜中,视网膜神经节细胞(RGC)轴突会向视裂方向延伸,尽管不存在明显的方向限制。先前的研究表明,轴突与基质的相互作用对视网膜神经节细胞轴突的延伸很重要,但引导延伸的因素尚不清楚。硫酸软骨素蛋白聚糖(CS-PG)是细胞外基质的一种成分,在体外能排斥背根神经节(DRG)轴突的延伸,并且在脊髓顶板中也有表达,脊髓顶板在发育过程中是DRG轴突延伸的一个屏障。在本研究中,我们检测了CS-PG是否可能调节发育中视网膜内视网膜神经节细胞的生长模式。免疫细胞化学分析显示,CS-PG存在于发育中大鼠视网膜的最内层。随着视网膜的发育,CS-PG的表达向周边移动,始终位于发育中轴突前端的外边缘。当视网膜中RGC轴突延伸完成后,用免疫细胞化学技术就检测不到CS-PG了。体外研究结果表明,从牛鼻软骨和鸡肢中分离出CS-PG对RGC轴突的延伸具有抑制作用,并且在相同CS-PG浓度下,RGC生长锥比DRG神经突对CS-PG更敏感。利用延时视频显微镜观察了视网膜生长锥遇到CS-PG时的行为。RGC生长锥的丝状伪足会反复延伸到CS-PG并对其进行探测。随着时间的推移,生长锥会转向避开CS-PG上的生长,仅在层粘连蛋白上生长。虽然许多研究已经表明视网膜中存在可能引导发育中RGC轴突的正向因子,但这是首次证明视网膜中存在一种可能调节轴突延伸的抑制性或排斥性分子。综上所述,这些数据表明,视网膜中RGC生长的方向可能由促进生长的分子(如层粘连蛋白)与抑制生长的分子(如CS-PG)的适当比例来调节,这些分子沿着视网膜神经节细胞通路以正确的模式和浓度存在。

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