Suppr超能文献

[突变型颤抖小鼠的遗传性脱髓鞘(繁殖与光学显微镜检查)]

[Hereditary demyelination in mutant quaking mice (breeding and light microscopy)].

作者信息

Zhabotinskiĭ Iu M, Chumasov E I, Shefer V F

出版信息

Arkh Patol. 1983;45(2):48-53.

PMID:6847412
Abstract

Data on breeding of mutant Quaking mice (MQM) and the results of light microscopy and morphometric examination of the central and peripheral nervous systems in them and in control mice varying in ages from 12 days to 4 months are presented. MQM were shown to have a decreased total volume of the white matter due to underdevelopment of myelin because of disturbed function of myelin-forming cells (oligodendrocytes). At the same time oligodendrocytes retain their capacity for proliferation and are normally located interfascicularly in the white matter having the same density of occurrence and the same average volume of the nucleus as in controls, but morphologically they are similar to oligodendroblasts. Another morphological feature of MQM consists of intensive vacuolation of their gray and white matter. However, light microscopy could not determine whether the vacuoles 1 to 9 microns in diameter were located intra- or extracellularly. No pathological changes in neurocytes, astrocytes or capillaries were observed.

摘要

本文呈现了突变型震颤小鼠(MQM)的繁殖数据,以及对它们和年龄从12天到4个月不等的对照小鼠的中枢和外周神经系统进行光学显微镜检查及形态计量学分析的结果。结果显示,由于髓鞘形成细胞(少突胶质细胞)功能紊乱导致髓鞘发育不全,MQM的白质总体积减小。同时,少突胶质细胞保留了增殖能力,正常位于白质束间,其出现密度和细胞核平均体积与对照组相同,但形态上类似于成少突胶质细胞。MQM的另一个形态学特征是其灰质和白质出现大量空泡化。然而,光学显微镜无法确定直径1至9微米的空泡是位于细胞内还是细胞外。未观察到神经细胞、星形胶质细胞或毛细血管的病理变化。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验