Sashihara S, Greer C A, Oh Y, Waxman S G
Department of Neurology, Yale University School of Medicine, New Haven, Connecticut 06510, USA.
J Neurosci. 1996 Jan 15;16(2):702-13. doi: 10.1523/JNEUROSCI.16-02-00702.1996.
Activity-dependent mechanisms have been implicated in olfactory system development but, although such activity requires ion channels, few reports have described their expression in the olfactory system. We investigated the developmental and denervation-induced regulation of the Na(+)-channel beta 1 subunit (Na beta 1) in rat olfactory bulb (OB) and piriform cortex (PC). In situ hybridization shows that Na beta 1 mRNA expression is upregulated developmentally, but with different time courses in mitral, tufted, and pyramidal cells. In mitral cells, label was detected at postnatal day 4 (P4) and gradually increased to P14. Tufted cells were devoid of Na beta 1 mRNA before P14, when most cells expressed adult levels. In pyramidal cells of PC, Na beta 1 expression was not detectable clearly until P14, with maximal expression at P28. To examine the regulation of Na beta 1 mRNA, we surgically deafferented the OB at P30 and compared the effects on Na beta 1 with those for Na(+)-channel alpha-subunit (Na alpha) mRNAs. Within 5 d of surgery, the Na beta 1 and Na alpha II signals within tufted cells disappeared almost completely. Na beta 1 and Na alpha II expression was decreased in mitral cells to low-to-moderate levels. In pyramidal cells, Na beta 1 mRNA expression was decreased moderately without significant changes in Na alpha II mRNA. Deafferentation had no detectable effects on Na alpha I or III mRNAs in either OB or PC. These data indicate that Na beta 1 mRNA is expressed differentially in subpopulations of cells in the olfactory system during development and after deafferentation and suggest that the expression of Na beta 1 is regulated independently of Na alpha mRNAs via cell-specific and pathway-specific mechanisms.
与活动相关的机制已被认为与嗅觉系统发育有关,然而,尽管这种活动需要离子通道,但很少有报道描述它们在嗅觉系统中的表达。我们研究了大鼠嗅球(OB)和梨状皮质(PC)中Na(+)通道β1亚基(Naβ1)的发育及去神经支配诱导的调节。原位杂交显示,Naβ1 mRNA表达在发育过程中上调,但在二尖瓣细胞、簇状细胞和锥体细胞中的时间进程不同。在二尖瓣细胞中,出生后第4天(P4)检测到标记,并逐渐增加至P14。簇状细胞在P14之前没有Naβ1 mRNA,此时大多数细胞表达成年水平。在PC的锥体细胞中,直到P14才清晰检测到Naβ1表达,在P28时表达最高。为了研究Naβ1 mRNA的调节,我们在P30对OB进行手术去神经支配,并将对Naβ1的影响与对Na(+)通道α亚基(Naα)mRNA的影响进行比较。在手术5天内,簇状细胞内的Naβ1和NaαII信号几乎完全消失。二尖瓣细胞中的Naβ1和NaαII表达降低至低到中等水平。在锥体细胞中,Naβ1 mRNA表达适度降低,而NaαII mRNA没有显著变化。去神经支配对OB或PC中的NaαI或III mRNA没有可检测到的影响。这些数据表明,Naβ1 mRNA在嗅觉系统发育过程中和去神经支配后在细胞亚群中差异表达,并表明Naβ1的表达通过细胞特异性和途径特异性机制独立于Naα mRNA进行调节。