[Glial and neuronal cellular changes in the glaucomatous human retina].

S Thanos, J M Rorbach, H J Thiel
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Abstract

The purpose of the present study was analysis of the cellular response to glaucoma in the human retina. Retinal strips obtained from two enucleated eyes with therapy-resistant, absolute glaucoma were explanted and cultured in vitro. The morphology of the remaining cell populations was assessed with the DiI method in non-cultured, formalin-fixed retinal tissue from both retinas. We found immunohistochemically identifiable glia cells migrating out from the explants and glial processes formed on the substrate. Labelling of representative retinal areas with the fluorescent dye DiI applied to the nerve fiber layer resulted in delineation of growth cone-bearing glial processes, of occasional non-atrophied ganglion cells, and of amacrines and horizontal cells in deeper layers of the retina. The results demonstrate that glaucoma leads both to selective damage of ganglion cells and to a glial proliferation characterized by the formation of processes both in the retina and following explantation.

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青光眼患者视网膜胶质细胞和神经元细胞的变化。
本研究的目的是分析细胞对青光眼在人视网膜的反应。从两个治疗抵抗性绝对青光眼的去核眼获得视网膜条,并在体外培养。其余细胞群的形态用DiI方法在非培养的,福尔马林固定的视网膜组织中进行评估。我们发现免疫组织化学可识别的胶质细胞从外植体中迁移出来,并在基质上形成胶质过程。将荧光染料DiI应用于神经纤维层,对代表性视网膜区域进行标记,结果描绘出生长锥状胶质突起,偶有未萎缩的神经节细胞,以及视网膜较深层的无突细胞和水平细胞。结果表明,青光眼导致神经节细胞的选择性损伤和神经胶质增生,其特征是在视网膜和外植后形成突起。
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