Gong B, Rhodes K J, Bekele-Arcuri Z, Trimmer J S
Department of Biochemistry and Cell Biology and Institute for Cell and Developmental Biology, State University of New York, Stony Brook, New York 11794-5215, USA.
J Comp Neurol. 1999 Sep 20;412(2):342-52.
Here we investigate differences in the temporal and spatial patterning, and subunit interactions of two of the major Na(+) channel alpha-subunit isoforms in mammalian brain, the type I and type II Na(+) channels. By using subtype-specific antibodies, we find that both isoforms are abundant in adult rat brain, where both interact with the covalently bound beta2 auxiliary subunit. Immunoblot analysis reveals complementary levels of type I and type II in different brain regions, with the highest levels of type I in brainstem, cortex, substantia nigra, and caudate, where it is found predominantly on the soma of neurons, and the highest levels of type II in globus pallidus, hippocampus and thalamus, where it is preferentially localized to axons. Developmentally, type I Na(+) channel polypeptide expression in brain increases dramatically during the third postnatal week, peaks at the end of the first postnatal month, and then decreases such that adult levels are approximately 50% of those at peak. Type II Na(+) channel polypeptide expression in brain also undergoes large increases in the third postnatal week, but levels continue to increase such that peak expression levels are maintained in adult animals. Type I Na(+) channels are found associated with the auxiliary beta2 subunit at all ages, whereas free type II Na(+) channels exist during the first two postnatal weeks. Thus, although expression of these two Na(+) channel alpha subunits in heterologous systems yields currents with very similar electrophysiological and pharmacological properties, their distinct spatial and temporal patterning, and association with auxiliary subunits in brain, suggest that they perform distinct, nonoverlapping functions in situ.
在此,我们研究了哺乳动物大脑中两种主要的Na⁺通道α亚基亚型(I型和II型Na⁺通道)在时间和空间模式以及亚基相互作用方面的差异。通过使用亚型特异性抗体,我们发现这两种亚型在成年大鼠脑中均大量存在,且都与共价结合的β2辅助亚基相互作用。免疫印迹分析显示,I型和II型在不同脑区的水平呈互补状态,I型在脑干、皮层、黑质和尾状核中水平最高,主要存在于神经元的胞体上;II型在苍白球、海马体和丘脑中水平最高,优先定位于轴突。在发育过程中,脑中I型Na⁺通道多肽的表达在出生后第三周急剧增加,在出生后第一个月末达到峰值,然后下降,使得成年水平约为峰值时的50%。脑中II型Na⁺通道多肽的表达在出生后第三周也大幅增加,但水平持续上升,使得成年动物中维持峰值表达水平。I型Na⁺通道在所有年龄段都与辅助β2亚基相关联,而游离的II型Na⁺通道在出生后的前两周存在。因此,尽管这两种Na⁺通道α亚基在异源系统中的表达产生的电流具有非常相似的电生理和药理特性,但它们在脑中不同的空间和时间模式以及与辅助亚基的关联表明,它们在原位执行不同的、不重叠的功能。