Suppr超能文献

再生大鼠背根神经节神经元中外周蛋白和神经丝基因表达的差异调节

Differential regulation of peripherin and neurofilament gene expression in regenerating rat DRG neurons.

作者信息

Wong J, Oblinger M M

机构信息

Department of Cell Biology and Anatomy, Chicago Medical School, North Chicago 60064.

出版信息

J Neurosci Res. 1990 Nov;27(3):332-41. doi: 10.1002/jnr.490270312.

Abstract

Quantitative in situ hybridization and RNA blotting methods were used to define the time course and magnitude of changes in expression of mRNAs encoding peripherin and the neurofilament (NF) triplet proteins in rat dorsal root ganglion (DRG) neurons during axonal regeneration. mRNA levels in adult rat L4 and L5 DRGs were examined in autoradiograms after in situ hybridization with specific 35S-labeled cDNA probes 1-56 days following unilateral crush lesions of the sciatic nerve. The results of quantitative analyses indicated that peripherin mRNA levels were significantly increased in large-sized (greater than 1000 microns 2) DRG neurons at 7, 14, and 28 days after axotomy while the mRNA levels for each of the NF triplet proteins were significantly decreased at these same time points. The mRNA levels of the low (NF-L) and middle (NF-M) sized NF subunits were significantly decreased as early as 1 day postaxotomy but the mRNA level of the large NF subunit (NF-H) did not change until 7 days after axotomy. The maximal reduction in NF mRNA levels was observed at 14 days postaxotomy when NF-L mRNA levels were only 35% of those in large-sized, normal control neurons. Recovery toward normal levels of both NF and peripherin mRNAs was observed at 8 weeks postaxotomy. RNA blot analyses with total RNA obtained from DRGs at different postaxotomy times confirmed that NF-L mRNA levels were reduced in the DRG during the first 4 weeks after axotomy but, interestingly, failed to detect an increase in peripherin mRNA levels. This difference concerning peripherin mRNA levels in axotomized preparations obtained by RNA blotting vs. in situ hybridization was attributed to the fact that RNA blots utilized total DRG RNA which includes mRNAs from both small and large-sized DRG neurons. A recent in situ hybridization study showed that the small-sized DRG neurons which contain the majority of the peripherin mRNA in the DRG do not increase their peripherin mRNA levels 14 days after axotomy (Oblinger et al., 1989b). This may mask any change in the large neuron response when total RNA is examined. Overall, the results of this study demonstrate (1) that type III (peripherin) and type IV (NF) intermediate filament genes are regulated differently during axonal regeneration, and (2) that the three NF genes are down-regulated in a fairly coordinate manner during regeneration. These data suggest that an important component of the regeneration program is the alteration of the composition of the IF component of the cytoskeleton.(ABSTRACT TRUNCATED AT 400 WORDS)

摘要

采用定量原位杂交和RNA印迹法来确定大鼠背根神经节(DRG)神经元轴突再生过程中,编码外周蛋白和神经丝(NF)三联体蛋白的mRNA表达变化的时间进程和幅度。在坐骨神经单侧挤压损伤后1 - 56天,用特异性35S标记的cDNA探针进行原位杂交后,在放射自显影片中检测成年大鼠L4和L5 DRG中的mRNA水平。定量分析结果表明,轴突切断后7天、14天和28天,大型(大于1000微米2)DRG神经元中外周蛋白mRNA水平显著升高,而在这些相同时间点,NF三联体蛋白各自的mRNA水平均显著降低。低分子量(NF-L)和中分子量(NF-M)NF亚基的mRNA水平早在轴突切断后1天就显著降低,但大型NF亚基(NF-H)的mRNA水平直到轴突切断后7天才发生变化。在轴突切断后14天观察到NF mRNA水平的最大降幅,此时NF-L mRNA水平仅为大型正常对照神经元的35%。在轴突切断后8周观察到NF和外周蛋白mRNA水平恢复至正常水平。对轴突切断后不同时间从DRG获得的总RNA进行RNA印迹分析证实,轴突切断后的前4周DRG中NF-L mRNA水平降低,但有趣的是,未检测到外周蛋白mRNA水平的升高。RNA印迹法与原位杂交法在轴突切断标本中外周蛋白mRNA水平上的这种差异归因于RNA印迹法使用的是DRG总RNA,其中包括来自小型和大型DRG神经元的mRNA。最近一项原位杂交研究表明,DRG中含有大部分外周蛋白mRNA的小型DRG神经元在轴突切断后14天其外周蛋白mRNA水平并未升高(Oblinger等人,1989b)。当检测总RNA时,这可能掩盖了大型神经元反应中的任何变化。总体而言,本研究结果表明:(1)III型(外周蛋白)和IV型(NF)中间丝基因在轴突再生过程中受到不同调控;(2)在再生过程中,三个NF基因以相当协调的方式被下调。这些数据表明,再生程序的一个重要组成部分是细胞骨架中间丝成分组成的改变。(摘要截于400字)

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验