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大鼠背根神经节神经元中外周和中枢轴突切断对神经丝和微管蛋白基因表达影响的比较。

A comparison of peripheral and central axotomy effects on neurofilament and tubulin gene expression in rat dorsal root ganglion neurons.

作者信息

Wong J, Oblinger M M

机构信息

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

出版信息

J Neurosci. 1990 Jul;10(7):2215-22. doi: 10.1523/JNEUROSCI.10-07-02215.1990.

Abstract

The expression of major cytoskeletal protein mRNAs was studied in adult rat dorsal root ganglion (DRG) neurons after crushing either their central or peripheral branch axons. mRNA levels in DRG neurons were examined by quantitative in situ hybridization with radiolabeled cDNA probes specific for the low-molecular-weight neurofilament protein (NF-L) and beta-tubulin. The large-sized (greater than 1000 microns 2) neurons which give rise to myelinated axons in lumbar ganglia (L4 and L5) were studied 1 d through 8 weeks after either dorsal root or sciatic nerve crush. NF-L and beta-tubulin mRNA levels in axotomized DRG neurons were compared to those in contralateral control DRG neurons, as well as to those in normal (completely untreated) DRG cells. In the case of NF-L mRNA, changes were observed after central as well as peripheral branch axotomy and the time course and magnitude of changes were similar after both types of axotomy. NF-L mRNA levels initially decreased (first 2 weeks after crush) and then began to return towards control levels at longer survival times. Similar, but less pronounced, changes in NF-L mRNA levels also occurred in contralateral DRG neurons (which were uninjured); the changes in contralateral neurons were not simply a result of surgical stress since no changes in NF-L mRNA levels were observed in sham-operated DRG neurons. In the case of tubulin mRNA, changes were observed after central as well as peripheral branch axotomy by in situ hybridization, but the time course and magnitude of changes were different after each type of axotomy.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

在成年大鼠背根神经节(DRG)神经元中,对其中枢或外周分支轴突进行挤压损伤后,研究了主要细胞骨架蛋白mRNA的表达。通过用针对低分子量神经丝蛋白(NF-L)和β-微管蛋白的放射性标记cDNA探针进行定量原位杂交,检测DRG神经元中的mRNA水平。对腰神经节(L4和L5)中产生有髓轴突的大型(大于1000平方微米)神经元,在背根或坐骨神经挤压损伤后1天至8周进行研究。将轴突切断的DRG神经元中的NF-L和β-微管蛋白mRNA水平与对侧对照DRG神经元以及正常(完全未处理)DRG细胞中的水平进行比较。就NF-L mRNA而言,在中枢和外周分支轴突切断后均观察到变化,且两种类型轴突切断后变化的时间进程和幅度相似。NF-L mRNA水平最初下降(挤压后前2周),然后在更长的存活时间开始恢复到对照水平。在未受伤的对侧DRG神经元中也出现了类似但不太明显的NF-L mRNA水平变化;对侧神经元的变化并非仅仅是手术应激的结果,因为在假手术的DRG神经元中未观察到NF-L mRNA水平的变化。就微管蛋白mRNA而言,通过原位杂交在中枢和外周分支轴突切断后均观察到变化,但每种类型轴突切断后变化的时间进程和幅度不同。(摘要截短至250字)

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