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共济失调和雄性不育(AMS)突变小鼠小脑中不同类型的神经细胞死亡

Different types of neural cell death in the cerebellum of the ataxia and male sterility (AMS) mutant mouse.

作者信息

Zhou Li, Araki Asuka, Nakano Akinobu, Sezer Cem, Harada Takayuki

机构信息

Department of Pathology, Organ Pathology Unit, Shimane University School of Medicine, Izumo, Japan.

出版信息

Pathol Int. 2006 Apr;56(4):173-80. doi: 10.1111/j.1440-1827.2006.01943.x.

Abstract

To investigate the mechanisms(s) of age-dependent atrophy of the cerebellum of the ataxia and male sterility (AMS) mouse at young age, the morphological changes were evaluated and the nature of neural cell death was examined. Dying Purkinje cells lacked characters of classical apoptosis except for light microscopic morphology, but their death was considered to be autonomous death triggered by the direct effect of ams mutation, because of the acute and near-complete disappearance and particular change of the cytoplasm. In contrast, in the granular layer, typical apoptotic bodies were recognized by electron microscopy, and substantial numbers of terminal deoxynucleotidyl transferase-mediated deoxyuridine triphosphate nick-end-labeling (TUNEL)-positive cells and activated caspase-3-positive cells were observed. Granule cell death was considered to be target-related apoptosis induced after post-synaptic Purkinje cell death, because the age-dependent changes in TUNEL-positive cell counts followed that of Purkinje cell loss and the peak value was still noted 1 week after total loss of Purkinje cells. These results indicate that both total and partial losses of Purkinje cells and granule cells, respectively, contributed to the atrophy of the AMS cerebellum. Furthermore, different types of neuronal death were recognized; the granule cell death was apoptotic while Purkinje cell death was different from that of classical apoptosis.

摘要

为了研究共济失调和雄性不育(AMS)小鼠年轻时小脑年龄依赖性萎缩的机制,评估了其形态学变化并检查了神经细胞死亡的性质。濒死的浦肯野细胞除了光镜形态外缺乏经典凋亡的特征,但其死亡被认为是由ams突变的直接作用引发的自主死亡,因为细胞质会急性且几乎完全消失并发生特定变化。相比之下,在颗粒层,通过电子显微镜可识别出典型的凋亡小体,并且观察到大量的末端脱氧核苷酸转移酶介导的脱氧尿苷三磷酸缺口末端标记(TUNEL)阳性细胞和活化的半胱天冬酶-3阳性细胞。颗粒细胞死亡被认为是突触后浦肯野细胞死亡后诱导的与靶点相关的凋亡,因为TUNEL阳性细胞计数的年龄依赖性变化跟随浦肯野细胞丢失的变化,并且在浦肯野细胞完全丢失1周后仍可观察到峰值。这些结果表明,浦肯野细胞和颗粒细胞分别全部和部分丢失导致了AMS小鼠小脑的萎缩。此外,还识别出了不同类型的神经元死亡;颗粒细胞死亡是凋亡性的,而浦肯野细胞死亡与经典凋亡不同。

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