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染料诱导的哺乳动物神经元在体内的“光变性”和“光通透化”

Dye-induced 'photo-degeneration' and 'photo-permeabilization' of mammalian neurons in vivo.

作者信息

Picaud S, Peichl L, Franceschini N

机构信息

Max-Planck Institut für Hirnforschung, Frankfurt, F.R.G.

出版信息

Brain Res. 1990 Oct 29;531(1-2):117-26. doi: 10.1016/0006-8993(90)90764-3.

Abstract

Dyes are known to induce neuronal 'photo-degeneration' and 'photo-permeabilization' in fly photoreceptor cells in vivo. In the present study, we attempted to generalize this photodynamic damage to vertebrate neurons, using the rat retina, a brain part which is optically accessible in vivo. After intravitreal injection of the photosensitizing dye Rose Bengal (RB), irradiation of the retina of a living rat with a T-shaped microbeam was found to induce striking 'optograms' which could be observed on the excised retina. The T-shaped pattern which was to be seen in the translucent retina under transmitted light was attributed to neuronal degeneration of the neurons irradiated in the presence of RB, as attested by classical degenerative features such as a cytoplasmic darkening or a drastic swelling. The T-shaped pattern could also be observed on adding the dye Lucifer yellow to the extracellular space of the retina either in vitro or in vivo, showing that the cells irradiated in the presence of RB became permeable. These structural reactions were observed in the cells in the inner nuclear layer (INL) and ganglion cell layer (GCL), in the processes in both plexiform layers, and in the ganglion cell axons crossing this area, whereas the photoreceptors in the outer retina appeared to be undamaged. From these reactions, due to photo-degeneration and photo-permeabilization, it was possible to identify the photodynamic damage to the nervous system histologically at the macroscopic, cellular and ultrastructural levels. In view of its accuracy and reproducibility, the photo-lesion technique holds great potential as a tool for investigating various nervous systems.

摘要

已知染料可在体内诱导果蝇光感受器细胞发生神经元“光变性”和“光通透化”。在本研究中,我们试图将这种光动力损伤推广至脊椎动物神经元,采用大鼠视网膜,这是一个在体内可进行光学观察的脑区。玻璃体内注射光敏染料孟加拉玫瑰红(RB)后,用T形微束照射活体大鼠的视网膜,发现可诱导出明显的“视像”,在切除的视网膜上可以观察到。在透射光下在半透明视网膜中看到的T形图案归因于在RB存在下被照射神经元的神经变性,如细胞质变暗或剧烈肿胀等经典变性特征所证实。在体外或体内向视网膜的细胞外空间添加染料荧光黄时也可观察到T形图案,表明在RB存在下被照射的细胞变得通透。在内核层(INL)和神经节细胞层(GCL)的细胞中、两个神经纤维层的突起中以及穿过该区域的神经节细胞轴突中观察到了这些结构反应,而外视网膜中的光感受器似乎未受损。基于这些由光变性和光通透化引起的反应,有可能在宏观、细胞和超微结构水平上从组织学上识别对神经系统的光动力损伤。鉴于其准确性和可重复性,光损伤技术作为研究各种神经系统的工具具有巨大潜力。

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