Department of Neurosurgery, Chang Gung Memorial Hospital - Kaohsiung Medical Center, Chang Gung University College of Medicine, Taiwan.
BMC Musculoskelet Disord. 2010 Aug 12;11:181. doi: 10.1186/1471-2474-11-181.
To compare the microRNA (miRNA) expression profiles in neurons and innervated muscles after sciatic nerve entrapment using a non-constrictive silastic tube, subsequent surgical decompression, and denervation injury.
The experimental L4-L6 spinal segments, dorsal root ganglia (DRGs), and soleus muscles from each experimental group (sham control, denervation, entrapment, and decompression) were analyzed using an Agilent rat miRNA array to detect dysregulated miRNAs. In addition, muscle-specific miRNAs (miR-1, -133a, and -206) and selectively upregulated miRNAs were subsequently quantified using real-time reverse transcription-polymerase chain reaction (real-time RT-PCR).
In the soleus muscles, 37 of the 47 miRNAs (13.4% of the 350 unique miRNAs tested) that were significantly downregulated after 6 months of entrapment neuropathy were also among the 40 miRNAs (11.4% of the 350 unique miRNAs tested) that were downregulated after 3 months of decompression. No miRNA was upregulated in both groups. In contrast, only 3 miRNAs were upregulated and 3 miRNAs were downregulated in the denervated muscle after 6 months. In the DRGs, 6 miRNAs in the entrapment group (miR-9, miR-320, miR-324-3p, miR-672, miR-466b, and miR-144) and 3 miRNAs in the decompression group (miR-9, miR-320, and miR-324-3p) were significantly downregulated. No miRNA was upregulated in both groups. We detected 1 downregulated miRNA (miR-144) and 1 upregulated miRNA (miR-21) after sciatic nerve denervation. We were able to separate the muscle or DRG samples into denervation or entrapment neuropathy by performing unsupervised hierarchal clustering analysis. Regarding the muscle-specific miRNAs, real-time RT-PCR analysis revealed an approximately 50% decrease in miR-1 and miR-133a expression levels at 3 and 6 months after entrapment, whereas miR-1 and miR-133a levels were unchanged and were decreased after decompression at 1 and 3 months. In contrast, there were no statistical differences in the expression of miR-206 during nerve entrapment and after decompression. The expression of muscle-specific miRNAs in entrapment neuropathy is different from our previous observations in sciatic nerve denervation injury.
This study revealed the different involvement of miRNAs in neurons and innervated muscles after entrapment neuropathy and denervation injury, and implied that epigenetic regulation is different in these two conditions.
本研究通过使用非缩窄性硅橡胶管、随后的手术减压和去神经损伤,比较坐骨神经嵌压后神经元和神经支配肌肉中的 microRNA (miRNA) 表达谱。
对每组(假手术对照、去神经支配、嵌压和减压)的实验性 L4-L6 脊髓节段、背根神经节 (DRG) 和比目鱼肌进行分析,使用 Agilent 大鼠 miRNA 阵列检测失调的 miRNA。此外,使用实时逆转录-聚合酶链反应 (real-time RT-PCR) 随后定量检测肌肉特异性 miRNA(miR-1、-133a 和 -206)和选择性上调的 miRNA。
在比目鱼肌中,在嵌压神经病 6 个月后显著下调的 37 个 miRNA(在 350 个独特 miRNA 中测试的 13.4%)也在 3 个月后减压时下调的 40 个 miRNA(在 350 个独特 miRNA 中测试的 11.4%)中。在两组中均未上调 miRNA。相比之下,在 6 个月时,去神经支配的肌肉中仅上调了 3 个 miRNA,下调了 3 个 miRNA。在 DRG 中,嵌压组中有 6 个 miRNA(miR-9、miR-320、miR-324-3p、miR-672、miR-466b 和 miR-144)和减压组中有 3 个 miRNA(miR-9、miR-320 和 miR-324-3p)显著下调。两组均未上调 miRNA。在坐骨神经去神经支配后,我们检测到 1 个下调的 miRNA(miR-144)和 1 个上调的 miRNA(miR-21)。通过进行无监督层次聚类分析,我们能够将肌肉或 DRG 样本分为去神经支配或嵌压神经病。关于肌肉特异性 miRNA,实时 RT-PCR 分析显示,在嵌压后 3 个月和 6 个月,miR-1 和 miR-133a 的表达水平降低了约 50%,而 miR-1 和 miR-133a 的水平在减压后 1 个月和 3 个月时没有变化并降低。相比之下,miR-206 的表达在神经嵌压和减压后没有统计学差异。在嵌压神经病中,肌肉特异性 miRNA 的表达与我们之前在坐骨神经去神经损伤中的观察结果不同。
本研究揭示了 miRNA 在嵌压神经病和去神经损伤后神经元和神经支配肌肉中的不同参与,并暗示了这两种情况下表观遗传调控的不同。