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小鼠脑钾通道β1亚基mRNA:克隆及发育过程中的分布

Mouse brain potassium channel beta1 subunit mRNA: cloning and distribution during development.

作者信息

Butler D M, Ono J K, Chang T, McCaman R E, Barish M E

机构信息

Division of Neurosciences, Beckman Research Institute of the City of Hope, Duarte, California 91010, USA.

出版信息

J Neurobiol. 1998 Feb 5;34(2):135-50.

PMID:9468385
Abstract

The pore-forming alpha subunits of voltage-gated potassium channels in neurons and other excitable cells are expressed in association with accessory beta subunits. These subunits both promote insertion of channel complexes into surface membranes and influence their electrophysiological properties. As part of an effort to understand the regulation of voltage-gated potassium channels during development, we cloned the mouse homolog of the rat Kvbeta1 potassium channel subunit. Kvbeta1 subunits are known to associate preferentially with Shaker (Kv1)-related alpha subunits. We then used a digoxigenin-tagged cRNA probe and in situ hybridization techniques to visualize the appearance of Kvbeta1 mRNA transcripts during late embryonic and early neonatal development of the mouse brain. We detected Kvbeta1-specific labeling of cells in hippocampus, cerebral cortex, caudate putamen, colliculus, and cerebellum. In hippocampus, we observed Kvbeta1 mRNA in CA3 pyramidal neurons at the earliest time examined, embryonic day 16 (E16). Between E16 and postnatal day 7 (P7), cell labeling increased uniformly across the pyramidal neurons of Ammon's horn (CA1, CA2, and CA3). Subsequently, between P7 and P22, regional differences characteristic of mature hippocampus appeared-intense labeling of neurons in CA3 and CA1, and less in CA2. In cortex, labeling of cells in the subplate and cortical plate layers was observed at E16. During development, the intensity of this labeling increased, and labeled cells persisted into the adult stage in the deep cortical layer (VIb) formed from subplate neurons. Additional labeling of scattered solitary cells in cortical layers II-VIa emerged between P3 and P7 and was prominent in mature cortex. In caudate putamen, Kvbeta1-labeled cells were observed at P1 and were restricted to the lateral and rostral half of the caudate. During development, labeling expanded caudally and medially and eventually filled the mature caudate putamen. In colliculus, a small population of inferior colliculus cells showed labeling at P7, and additional labeling of scattered cells appeared during development. In superior colliculus, labeling was observed only in the adult deep gray layer. In cerebellum, intense labeling was observed in Purkinje cells at all stages between P1 and adult. Labeling was also seen in granule neurons in the external granule layer at early postnatal stages and in the inner granule layer beginning at P7.

摘要

神经元和其他可兴奋细胞中电压门控钾通道的成孔α亚基与辅助β亚基共同表达。这些亚基既促进通道复合物插入细胞膜表面,又影响其电生理特性。作为了解发育过程中电压门控钾通道调控机制的一部分工作,我们克隆了大鼠Kvβ1钾通道亚基的小鼠同源物。已知Kvβ1亚基优先与Shaker(Kv1)相关的α亚基结合。然后,我们使用地高辛标记的cRNA探针和原位杂交技术来观察小鼠脑胚胎后期和新生儿早期发育过程中Kvβ1 mRNA转录本的出现情况。我们在海马体、大脑皮层、尾状壳核、丘和小脑中检测到了Kvβ1特异性标记的细胞。在海马体中,我们在最早检测的时间点即胚胎第16天(E16),就在CA3锥体神经元中观察到了Kvβ1 mRNA。在E16到出生后第7天(P7)之间,整个海马角(CA1、CA2和CA3)的锥体神经元细胞标记均匀增加。随后,在P7到P22之间,成熟海马体特有的区域差异出现了——CA3和CA1中的神经元标记强烈,而CA2中的较少。在皮层中,在E16时观察到了板下层和皮质板层细胞的标记。在发育过程中,这种标记的强度增加,并且标记细胞在由板下层神经元形成的深层皮质层(VIb)中持续到成年期。在P3到P7之间,皮层II - VIa层中散在孤立细胞的额外标记出现,并在成熟皮层中很突出。在尾状壳核中,在P1时观察到Kvβ1标记的细胞,且仅限于尾状核的外侧和头侧半部分。在发育过程中,标记向尾侧和内侧扩展,最终充满成熟的尾状壳核。在丘中一小群下丘细胞在P7时显示出标记,并且在发育过程中出现了散在细胞的额外标记。在上丘中,仅在成年深灰色层中观察到标记。在小脑中,在P1到成年期的所有阶段浦肯野细胞中都观察到强烈标记。在出生后早期阶段外颗粒层中的颗粒神经元以及从P7开始的内颗粒层中也观察到标记。

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