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颗粒细胞存活在PAC1基因敲除突变小鼠的小脑中存在缺陷。

Granule cell survival is deficient in PAC1-/- mutant cerebellum.

作者信息

Falluel-Morel Anthony, Tascau Liana I, Sokolowski Katie, Brabet Philippe, DiCicco-Bloom Emanuel

机构信息

Department of Neuroscience and Cell Biology, UMDNJ-Robert Wood Johnson Medical School, 675 Hoes Lane, Room RWJSPH 362, Piscataway, NJ 08854, USA.

出版信息

J Mol Neurosci. 2008 Nov;36(1-3):38-44. doi: 10.1007/s12031-008-9066-6. Epub 2008 Apr 12.

Abstract

PACAP exerts neuroprotective effects during development, especially in the cerebellum where PAC1 receptor and ligand are both expressed. However, while previous studies using PACAP injections in postnatal animals defined trophic effects of exogenous peptide, the role of endogenous PACAP remains unexplored. Here, we used PAC1(-/-) mice to investigate the role of PACAP receptor signaling in postnatal day 7 cerebellum. There was no difference in DNA synthesis in the cerebellar EGL of PAC1(-/-) compared to wild type animals, assessed using thymidine incorporation and BrdU immunohistochemistry. In contrast, we found that a significant proportion of newly generated neurons were eliminated before they successfully differentiated in the granule cell layer. In aggregate, these results suggest that endogenous PACAP plays an important role in cell survival during cerebellar development, through the activation of the PAC1 receptor.

摘要

垂体腺苷酸环化酶激活肽(PACAP)在发育过程中发挥神经保护作用,尤其是在同时表达PAC1受体和配体的小脑中。然而,尽管先前在出生后动物中注射PACAP的研究确定了外源性肽的营养作用,但内源性PACAP的作用仍未得到探索。在这里,我们使用PAC1基因敲除小鼠来研究PACAP受体信号在出生后第7天小脑发育中的作用。使用胸腺嘧啶核苷掺入法和BrdU免疫组化评估发现,与野生型动物相比,PAC1基因敲除小鼠小脑外颗粒层(EGL)中的DNA合成没有差异。相反,我们发现相当一部分新生成的神经元在颗粒细胞层成功分化之前就被清除了。总的来说,这些结果表明内源性PACAP通过激活PAC1受体在小脑发育过程中的细胞存活中发挥重要作用。

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