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热休克蛋白Hsp25在小鼠浦肯野细胞发育过程中的表达揭示了小脑分区的新特征。

Expression of heat-shock protein Hsp25 in mouse Purkinje cells during development reveals novel features of cerebellar compartmentation.

作者信息

Armstrong C L, Krueger-Naug A M, Currie R W, Hawkes R

机构信息

Department of Cell Biology & Anatomy, and Genes and Development Research Group, Faculty of Medicine, The University of Calgary, Calgary, Alberta T2N 4N1, Canada.

出版信息

J Comp Neurol. 2001 Jan 1;429(1):7-21. doi: 10.1002/1096-9861(20000101)429:1<7::aid-cne2>3.0.co;2-q.

Abstract

The small heat shock protein Hsp25 is constitutively expressed in the adult mouse cerebellum by parasagittal stripes of Purkinje cells confined to the caudal central zone ( approximately lobules VI and VII), the nodular zone ( approximately ventral lobule IX and lobule X), and the paraflocculi/flocculi. During development several distinct phases in Hsp25 expression can be distinguished. Hsp25-immunopositive Purkinje cells are first seen at birth, when four clusters are visible in the vermis of lobules IV/V, and scattered Hsp25-immunoreactive Purkinje cells are seen in lobule VIII. By postnatal day 2/3, six narrow parasagittal stripes of Hsp25-immunopositive Purkinje cells are seen in the vermis of the anterior lobe. In the posterior lobules, most Purkinje cells in the vermis of lobules VIII and IX express Hsp25. This initial limited expression is followed by a phase of widespread expression (postnatal days 6-9) in which Hsp25 immunoreactivity is detected in virtually all Purkinje cells. This global cerebellar expression of Hsp25 then gradually disappears, first in the anterior zone and the hemispheres and subsequently in the posterior zone, to leave the restricted adult expression pattern. Western blotting analysis and immunoprecipitation with anti-Hsp25 suggest that all immunocytochemistry can be attributed the expression of Hsp25. Furthermore, visual deprivation had no effect on the development of Hsp25 expression in Purkinje cells, suggesting that visuomotor input is not responsible for the establishment of constitutive Hsp25 expression in the cerebellar cortex.

摘要

小热休克蛋白Hsp25在成年小鼠小脑中由局限于尾侧中央区(大致为小叶VI和VII)、小结区(大致为腹侧小叶IX和小叶X)以及旁绒球/绒球的浦肯野细胞的矢状旁条纹组成性表达。在发育过程中,可以区分出Hsp25表达的几个不同阶段。Hsp25免疫阳性的浦肯野细胞在出生时首次出现,此时在小叶IV/V的蚓部可见四个簇,并且在小叶VIII中可见散在的Hsp25免疫反应性浦肯野细胞。到出生后第2/3天,在前叶蚓部可见六条狭窄的Hsp25免疫阳性浦肯野细胞的矢状旁条纹。在后部小叶中,小叶VIII和IX蚓部的大多数浦肯野细胞表达Hsp25。这种最初有限的表达之后是广泛表达阶段(出生后第6 - 9天),在此阶段几乎在所有浦肯野细胞中都检测到Hsp25免疫反应性。Hsp25在整个小脑的这种表达随后逐渐消失,首先在前区和半球,随后在后部区域,从而形成成年期受限的表达模式。蛋白质免疫印迹分析和用抗Hsp25进行免疫沉淀表明,所有免疫细胞化学结果都可归因于Hsp25的表达。此外,视觉剥夺对浦肯野细胞中Hsp25表达的发育没有影响,这表明视觉运动输入不是小脑皮质中组成性Hsp25表达建立的原因。

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