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帕金森病MPTP小鼠模型中脑室下区和吻侧迁移流的细胞凋亡证据。

Evidence of apoptosis in the subventricular zone and rostral migratory stream in the MPTP mouse model of Parkinson disease.

作者信息

He Xi Jun, Nakayama Hiroyuki, Dong Mei, Yamauchi Hirofumi, Ueno Masaki, Uetsuka Koji, Doi Kunio

机构信息

Department of Veterinary Pathology, Graduate School of Agricultural and Life Sciences, The University of Tokyo, Tokyo, Japan.

出版信息

J Neuropathol Exp Neurol. 2006 Sep;65(9):873-82. doi: 10.1097/01.jnen.0000235115.29440.ce.

Abstract

1-Methyl-4-phenyl-1,2,3,6-tetrahydropyridine (MPTP) is commonly used to create animal models of Parkinson disease. There is conflicting evidence on the occurrence of apoptosis induced by MPTP in the mouse substantia nigra pars compacta. We demonstrated that a single acute injection of MPTP induced apoptosis in the subventricular zone (SVZ) and rostral migratory stream (RMS) in the adult C57BL/6 mouse brain. The number of TUNEL-positive cells peaked at 24 hours after injection and decreased thereafter, paralleling the change in the number of cleaved caspase-3-positive cells after MPTP injection. Results of immunohistochemistry and ultrastructural analyses indicated that the majority of apoptotic cells in the SVZ and RMS were migrating neuroblasts (type A cells), whereas a few were astrocytes (type B cells). No apoptosis occurred in transit-amplifying progenitors (type C cells). The decrease in A cell numbers was most marked on day 2 and lasted to day 8 after the administration. A rapid and transient phagocytosis of apoptotic cells by microglial cells was demonstrated to parallel the MPTP-induced apoptosis. The present findings provide new insight into the extensive neurotoxicity of MPTP and may be valuable in reevaluating the MPTP mouse model of Parkinson disease.

摘要

1-甲基-4-苯基-1,2,3,6-四氢吡啶(MPTP)常用于建立帕金森病的动物模型。关于MPTP在小鼠黑质致密部诱导细胞凋亡的发生,存在相互矛盾的证据。我们证明,单次急性注射MPTP可诱导成年C57BL/6小鼠脑室内下区(SVZ)和吻侧迁移流(RMS)发生细胞凋亡。TUNEL阳性细胞数量在注射后24小时达到峰值,此后减少,与MPTP注射后裂解的半胱天冬酶-3阳性细胞数量的变化平行。免疫组织化学和超微结构分析结果表明,SVZ和RMS中的大多数凋亡细胞是迁移的神经母细胞(A型细胞),而少数是星形胶质细胞(B型细胞)。过渡增殖祖细胞(C型细胞)未发生凋亡。给药后第2天,A型细胞数量减少最为明显,并持续至第8天。小胶质细胞对凋亡细胞的快速、短暂吞噬与MPTP诱导的细胞凋亡平行。本研究结果为MPTP的广泛神经毒性提供了新的见解,可能对重新评估帕金森病的MPTP小鼠模型具有重要价值。

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