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患有巴滕病的绵羊神经元的体外培养。

In vitro culture of neurons from sheep with Batten disease.

作者信息

Kay G W, Hughes S M, Palmer D N

机构信息

Animal and Food Sciences Division, Lincoln University, Canterbury, New Zealand.

出版信息

Mol Genet Metab. 1999 May;67(1):83-8. doi: 10.1006/mgme.1999.2849.

Abstract

Specific storage of mitochondrial ATP synthase subunit c occurs in most forms of Batten disease, including the ovine form, but its relationship to the characteristic neurodegeneration is not clear. Storage occurs in most cell types but only neurons are functionally affected. Neurons were cultured from control and affected sheep. Ewes were superovulated and inseminated, and embryos were collected, frozen, stored, and later transplanted into surrogate dams for gestation at times to suit experimental demands. The optimal fetal age for cultures was investigated, from 50 to 125 days. There were no differences between control and affected embryos in this period of rapid growth. At 50 days brains consist of smooth-surfaced hemispheres and cerebellum with no obvious demarcation between gray and white matter. At 90 days they are like miniature adult brains. From 200 to 600 million viable cells were recovered from each fetus, regardless of age. DMEM/F12 with B27 was the most practical medium tested. Cell viability was not as good in medium containing serum. Treatment of surfaces with polylysine aided neuron adhesion. No developmental or viability differences were observed between normal and affected neuron cultures. At plating out cells were rounded. A day later single process outgrowths began. After 4 days these were over 200 microm and by Day 6 had created a network. Most neurons were bipolar. Neurons from 50 to 90-day old fetuses persisted in culture for over 100 days.

摘要

线粒体ATP合酶亚基c的特异性储存存在于包括绵羊型在内的大多数巴顿病形式中,但其与特征性神经退行性变的关系尚不清楚。储存发生在大多数细胞类型中,但只有神经元在功能上受到影响。从对照羊和患病羊中培养神经元。对母羊进行超数排卵和授精,收集胚胎,冷冻、储存,之后根据实验需求适时将胚胎移植到代孕母羊体内进行妊娠。研究了培养的最佳胎龄,范围是50至125天。在这个快速生长阶段,对照胚胎和患病胚胎之间没有差异。50天时,大脑由表面光滑的半球和小脑组成,灰质和白质之间没有明显界限。90天时,它们就像微型的成人大脑。无论胎龄如何,从每个胎儿中回收了2亿至6亿个活细胞。含有B27的DMEM/F12是测试的最实用培养基。含血清的培养基中细胞活力较差。用聚赖氨酸处理表面有助于神经元黏附。在正常和患病神经元培养物之间未观察到发育或活力差异。接种时细胞呈圆形。一天后开始长出单个突起。4天后,这些突起超过200微米,到第6天形成了一个网络。大多数神经元是双极的。来自50至90日龄胎儿的神经元在培养中持续了100多天。

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