20327Schepens Eye Research Institute of Massachusetts Ear and Eye, Harvard Medical School, Boston, MA, USA.
Department of Material Science and Engineering, 2167 Massachusetts Institute of Technology, Cambridge, MA, USA.
Cell Transplant. 2020 Jan-Dec;29:963689720964383. doi: 10.1177/0963689720964383.
The optic pathway glioma (OPG) is a slow-growing brain tumor that arises along the optic nerve or its downstream connections and causing vision to gradually worsen with time. This tumor forms in children with a genetic condition called neurofibromatosis type 1 (NF1), causing tumors to grow on nerves. In normal conditions, glial cells are there to support and protect nerve cells but, in NF1-OPG, glial cells have a genetic defect and grow out of control forming a tumor called a glioma. There are no rat models of NF1-OPG that can be used to explore various treatment options, and mouse models make interventional studies difficult due to their small eye size. We have created a model in which to study the progression of tumor growth in the optic nerve and establish the anatomical and functional consequences of the model and determine its suitability to serve as a surrogate for human disease. C6 rat glioma cells were injected into the optic nerve of Long-Evans rats and allowed to proliferate for 2 weeks. The eye clearly showed proptosis and lens opacity was observed, likely due to increased intraocular pressure caused by growing tumors. Hematoxylin-eosin staining showed marked cellularity, with hyperchromatism and pleomorphism. There was prominent area of necrosis with neoplastic cells palisading around the penumbra. Immunostaining with markers such as S100, β-tubulin III, Foxp3, CD45, Vimentin, and Ki67 confirmed low-grade tumor formation, with a mild immune response. Our results show the utility of a surgically induced rat model of OPG that may be used for exploring various treatment options for NF1 ocular tumors.
视神经胶质瘤(OPG)是一种缓慢生长的脑肿瘤,它沿着视神经或其下游连接物生长,导致视力随着时间的推移逐渐恶化。这种肿瘤发生在一种称为神经纤维瘤病 1 型(NF1)的遗传疾病的儿童中,导致肿瘤在神经上生长。在正常情况下,神经胶质细胞存在于那里以支持和保护神经细胞,但在 NF1-OPG 中,神经胶质细胞存在遗传缺陷并失控生长,形成一种称为神经胶质瘤的肿瘤。目前没有可以用于探索各种治疗选择的 NF1-OPG 大鼠模型,而由于眼睛较小,小鼠模型使得介入性研究变得困难。我们已经创建了一种模型,可以研究视神经中肿瘤生长的进展,并建立该模型的解剖学和功能后果,以确定其是否适合作为人类疾病的替代模型。C6 大鼠神经胶质瘤细胞被注射到长耳大鼠的视神经中,并允许其增殖 2 周。眼睛明显出现突出,晶状体混浊,可能是由于肿瘤生长引起的眼内压升高所致。苏木精-伊红染色显示明显的细胞密度,出现深染和多形性。有明显的坏死区,肿瘤细胞围绕着半影呈栅栏状排列。免疫染色显示 S100、β-微管蛋白 III、Foxp3、CD45、波形蛋白和 Ki67 等标志物阳性,证实了低度肿瘤形成,并伴有轻度免疫反应。我们的结果表明,该手术诱导的大鼠 OPG 模型具有实用性,可用于探索 NF1 眼部肿瘤的各种治疗选择。