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癫痫发作诱导苔藓纤维发芽后大鼠海马颗粒细胞中GAP-43的表达:原位杂交和免疫细胞化学研究

Expression of GAP-43 in the granule cells of rat hippocampus after seizure-induced sprouting of mossy fibres: in situ hybridization and immunocytochemical studies.

作者信息

Bendotti C, Pende M, Samanin R

机构信息

Laboratory of Neuropharmacology, Istituto di Ricerche Farmacologiche Mario Negri, Milan, Italy.

出版信息

Eur J Neurosci. 1994 Apr 1;6(4):509-15. doi: 10.1111/j.1460-9568.1994.tb00294.x.

DOI:10.1111/j.1460-9568.1994.tb00294.x
PMID:8025706
Abstract

The axonal growth-associated protein GAP-43 is believed to play some role in the synaptic remodelling that takes place in the hippocampus of adult rats after certain experimental lesions. GAP-43 mRNA is highly expressed in adult CA3 pyramidal cells but almost absent in the dentate granule cells. We analysed whether the sprouting of granule cell axons, the mossy fibres of the hippocampus, caused by kainic acid-induced seizures in adult rats was associated with any induction of GAP-43 mRNA in granule cells and with any changes in the immunostaining pattern of GAP-43 in the hippocampus. Increased GAP-43 mRNA expression was found to be induced in granule cells 18, 24 and 30 h after a systemic injection of kainic acid which induced generalized seizures in adult rats, and returned to control levels by 48 h post-treatment. No effect was observed in other regions of the hippocampus. However, when kainic acid was injected into 15-day-old rats, which responded with generalized seizures but no sprouting of mossy fibres, there was no induction of GAP-43 mRNA in the granule cells, suggesting a close relation between GAP-43 expression and sprouting of these cells. Seven days after kainic acid injections, GAP-43 immunostaining was decreased in the inner molecular layer of the dentate gyrus except for a thin supragranular band, whereas 30 days after treatment all animals showed increased GAP-43 immunoreactivity in the whole inner molecular layer.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

轴突生长相关蛋白GAP - 43被认为在成年大鼠海马体经特定实验性损伤后发生的突触重塑中发挥一定作用。GAP - 43 mRNA在成年CA3锥体细胞中高表达,但在齿状颗粒细胞中几乎不存在。我们分析了成年大鼠因海藻酸诱导癫痫发作导致的颗粒细胞轴突(海马体的苔藓纤维)萌发是否与颗粒细胞中GAP - 43 mRNA的诱导以及海马体中GAP - 43免疫染色模式的任何变化相关。发现在给成年大鼠全身注射海藻酸诱导全身性癫痫发作后18、24和30小时,颗粒细胞中诱导了GAP - 43 mRNA表达增加,并在治疗后48小时恢复到对照水平。在海马体的其他区域未观察到影响。然而,当将海藻酸注射到15日龄大鼠中时,大鼠出现全身性癫痫发作但苔藓纤维未萌发,颗粒细胞中未诱导GAP - 43 mRNA表达,这表明GAP - 43表达与这些细胞的萌发之间存在密切关系。海藻酸注射7天后,齿状回内分子层的GAP - 43免疫染色除了一条薄的颗粒上带外均减少,而治疗后30天,所有动物的整个内分子层均显示GAP - 43免疫反应性增加。(摘要截断于250字)

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