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颞叶癫痫小鼠模型中海马CA2区苔藓纤维发芽和锥体细胞分散

Mossy fiber sprouting and pyramidal cell dispersion in the hippocampal CA2 region in a mouse model of temporal lobe epilepsy.

作者信息

Häussler Ute, Rinas Katrin, Kilias Antje, Egert Ulrich, Haas Carola A

机构信息

Experimental Epilepsy Research, Department of Neurosurgery, University Medical Center Freiburg, Freiburg, 79106, Germany.

Faculty of Biology, University of Freiburg, Freiburg, 79104, Germany.

出版信息

Hippocampus. 2016 May;26(5):577-88. doi: 10.1002/hipo.22543. Epub 2015 Nov 5.

Abstract

Dentate granule cells and the hippocampal CA2 region are resistant to cell loss associated with mesial temporal lobe epilepsy (MTLE). It is known that granule cells undergo mossy fiber sprouting in the dentate gyrus which contributes to a recurrent, proepileptogenic circuitry in the hippocampus. Here it is shown that mossy fiber sprouting also targets CA2 pyramidal cell somata and that the CA2 region undergoes prominent structural reorganization under epileptic conditions. Using the intrahippocampal kainate mouse model for MTLE and the CA2-specific markers Purkinje cell protein 4 (PCP4) and regulator of G-Protein signaling 14 (RGS14), it was found that during epileptogenesis CA2 neurons survive and disperse in direction of CA3 and CA1 resulting in a significantly elongated CA2 region. Using transgenic mice that express enhanced green fluorescent protein (eGFP) in granule cells and mossy fibers, we show that the recently described mossy fiber projection to CA2 undergoes sprouting resulting in aberrant large, synaptoporin-expressing mossy fiber boutons which surround the CA2 pyramidal cell somata. This opens up the potential for altered synaptic transmission that might contribute to epileptic activity in CA2. Indeed, intrahippocampal recordings in freely moving mice revealed that epileptic activity occurs concomitantly in the dentate gyrus and in CA2. Altogether, the results call attention to CA2 as a region affected by MTLE-associated pathological restructuring.

摘要

齿状颗粒细胞和海马CA2区对与内侧颞叶癫痫(MTLE)相关的细胞丢失具有抗性。已知颗粒细胞在齿状回中发生苔藓纤维出芽,这有助于海马中形成一个反复出现的、促癫痫发生的神经回路。本文表明,苔藓纤维出芽也靶向CA2锥体细胞胞体,并且在癫痫状态下CA2区会发生显著的结构重组。利用MTLE的海马内注射红藻氨酸小鼠模型以及CA2特异性标记物浦肯野细胞蛋白4(PCP4)和G蛋白信号调节因子14(RGS14),研究发现,在癫痫发生过程中,CA2神经元存活并向CA3和CA1方向分散,导致CA2区显著拉长。使用在颗粒细胞和苔藓纤维中表达增强型绿色荧光蛋白(eGFP)的转基因小鼠,我们发现最近描述的向CA2投射的苔藓纤维会发生出芽,形成异常的、表达突触孔蛋白的大型苔藓纤维终扣,围绕着CA2锥体细胞胞体。这为突触传递改变创造了可能性,而这可能会导致CA2区的癫痫活动。实际上,对自由活动小鼠进行的海马内记录显示,癫痫活动在齿状回和CA2区同时发生。总之,这些结果提醒人们注意CA2区是一个受MTLE相关病理重组影响的区域。

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