中枢神经系统过度表达转化生长因子- β 1致小鼠先天性脑积水模型的超微结构分析。

G Aliev, J P Miller, D W Leifer, M E Obrenovich, J C Shenk, M A Smith, J C Lamanna, G Perry, D W Lust, A R Cohen
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引用次数: 0

摘要

本研究的目的是利用透射电子显微镜(TEM)阐明在中枢神经系统中过度表达细胞因子转化生长因子- β 1 (tgf - β 1)的一种新的先天性脑积水小鼠可复制模型的皮层灰质内发生的超微结构变化。在产后2天,从经过工程改造过表达tgf - β 1的小鼠群体中获得脑组织,并与野生型年龄匹配对照进行比较。用含有1.25%多聚甲醛和1.25%戊二醛的溶液在磷酸盐缓冲液中固定该组织至少3-4小时,然后切成40-50微米的切片。随机选择薄片,用醋酸铀酰和柠檬酸铅染色,在加速电压80 kV下,用JEOL-100CX或1200EX透射电镜分析。在tgf - β 1小鼠的整个皮质神经节中观察到明显的神经元和神经胶质病变。脑积水小鼠最显著的变化是细胞外液严重水肿,可能是由于脑脊液渗入皮质所致。此外,整个皮质可见细胞质基质的严重破坏,细胞器受损,线粒体受损尤其严重。我们的研究结果表明先天性脑积水可能与皮质组织的严重损伤有关。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Ultrastructural analysis of a murine model of congenital hydrocephalus produced by overexpression of transforming growth factor-beta1 in the central nervous system.

The purpose of this study was to elucidate using transmission electron microscopy (TEM) the ultrastructural changes that occur within the cortical gray matter of a novel reproducible model of congenital hydrocephalus in mice created to overexpress the cytokine transforming growth factor-beta1 (TGF-beta1) in the central nervous system. Brain tissue was obtained from mice from a colony engineered to overexpress TGF-beta1 at two days postpartum and compared to a wild-type aged-matched control. This tissue was fixed using a solution containing 1.25% paraformaldehyde and 1.25% glutaraldehyde in phosphate buffer at least 3-4 h and then cut into 40-50 microm sections. Randomly selected thin sections were stained with uranyl acetate and lead citrate, and then analyzed using a JEOL-100CX or 1200EX transmission electron microscope at accelerating voltage 80 kV. Dramatic neuronal and glial pathology was observed throughout the cortical neuropil in TGF-beta1 mice. The most striking change in the hydrocephalic mice was severe edema with extracellular fluid, possibly due to cerebrospinal fluid (CSF) penetration into the cortex. In addition, severe disruption of the cytoplasmic matrix was seen throughout the cortex, with damage to cellular organelles and particularly severe damage to mitochondria. Our results suggest that congenital hydrocephalus may be associated with significant damage to cortical tissue.

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