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神经突变小鼠小脑浦肯野细胞线粒体的超微结构变化

Ultrastructural changes in the mitochondria of cerebellar Purkinje cells of nervous mutant mice.

作者信息

Landis S C

出版信息

J Cell Biol. 1973 Jun;57(3):782-97. doi: 10.1083/jcb.57.3.782.

Abstract

The maturation of cerebellar Purkinje cells of normal and nervous (nr/nr) mutant mice has been studied by light and electron microscopy. In the mutant, 90% of Purkinje cells selectively degenerate between postnatal days 23 and 50. Losses are greater in lateral than medial regions. Other cerebellar neurons appear normal. The first morphological abnormality recognized is the presence of rounded mitochondria in perikarya of some Purkinje cells of the mutant at 9 days after birth. By 15 days, all nr/nr Purkinje cells contain spherical mitochondria and begin to deviate from the normal maturational sequence. Elaboration of the extensive dendritic tree halts midway and newly formed axon collateral fibers degenerate. In the perikaryon, the basal polysomal accumulation and climbing fiber-somatic spine synapses are sometimes abnormally retained. Cisternae of the Golgi apparatus and rough endoplasmic reticulum cease to form aligned stacks, and decrease in number, while polysomes dissociate into free ribosomes. These changes are progressive, culminating in cell death. Although every nr/nr Purkinje cell demonstrates spherical mitochondria, some cells survive the critical period, retain a near-normal complement of organelles, and reacquire normal-appearing mitochondria. The disorder appears intrinsic to Purkinje cells since all major classes of synapses were identified before cell death.

摘要

已通过光学显微镜和电子显微镜研究了正常小鼠和神经(nr/nr)突变小鼠小脑浦肯野细胞的成熟过程。在突变小鼠中,90%的浦肯野细胞在出生后第23天至50天之间选择性退化。外侧区域的损失比内侧区域更大。其他小脑神经元看起来正常。最早识别出的形态学异常是在出生后9天,突变小鼠的一些浦肯野细胞的胞体中出现圆形线粒体。到15天时,所有nr/nr浦肯野细胞都含有球形线粒体,并开始偏离正常的成熟序列。广泛的树突分支发育在中途停止,新形成的轴突侧支纤维退化。在胞体中,基底多核糖体聚集和攀缘纤维-体细胞棘突触有时会异常保留。高尔基体和粗面内质网的潴泡不再形成排列整齐的堆叠,数量减少,而多核糖体解离成游离核糖体。这些变化是渐进性的,最终导致细胞死亡。尽管每个nr/nr浦肯野细胞都表现出球形线粒体,但一些细胞在关键期存活下来,保留了接近正常的细胞器组成,并重新获得外观正常的线粒体。由于在细胞死亡前已识别出所有主要类型的突触,这种紊乱似乎是浦肯野细胞固有的。

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