Department of Otorhinolaryngology, CHA University College of Medicine, South Korea.
Department of Otorhinolaryngology, CHA University College of Medicine, South Korea.
Gene. 2022 Dec 15;845:146822. doi: 10.1016/j.gene.2022.146822. Epub 2022 Aug 19.
Deafferentation and compensatory neural plastic changes in the inferior colliculus (IC) have been suggested following single-sided deafness (SSD). We explored related miRNA changes in the IC of SSD rats using miRNA microarray analyses.
Eight-week-old rats were divided into control and SSD rats (n = 8 for each group). SSD rats underwent right-side cochlear ablation surgery, with the IC harvested two weeks post-surgery. miRNA microarray analysis was performed using GeneChip miRNA 4.0, microarray (Affymetrix Inc.). miRNAs whose expression levels differed between SSD and control rats with a fold-change ≥ 1.5 and P < 0.05 were examined using quantitative reverse transcription-polymerase chain reaction (qRT-PCR). Target genes of differentially expressed miRNAs were predicted using TargetScan software. The pathways related to predicted target genes were analyzed. mRNA levels of predicted target genes were estimated using qRT-PCR.
The expression of miR-15b-5p, miR-202-5p, and miR-212-3p was lower in the contralateral (left) IC of SSD rats than that of control rats. In SSD rats, miRNA expression levels in the contralateral IC were 0.45-, 0.25-, and 0.50-fold lower for miR-15b-5p, miR-202-5p, and miR-212-3p, respectively (P < 0.05). The expression of predicted target genes (Spred1, Rasa1, Lsm11, and Srsf1) was higher in the contralateral IC of SSD rats than in control rats. The targets were predicted to be related with cleavage of growing transcripts in the termination region, mitogen-activated protein kinase family signaling cascades, RAF/AMP kinase cascade, regulation of RAS by GTPase activating proteins (GAPs), and RNA polymerase II transcription termination. For ipsilateral ICs, miR-425-3p, miR-199a-5p, and miR-134-3p showed lower expressions in SSD rats than in control rats, which were 0.55-, 0.61-, and 0.69-fold lower, respectively (P < 0.05). The expression of predicted target genes (Atp2b2, Grin2b, Foxp1, Ztbt20, Zfp91, and Strn) was higher in the ipsilateral IC of SSD rats; the regulation of synaptic plasticity, cAMP signaling pathway, metal ion binding, and calcium ion transport can be associated with these target genes.
Adult rats with unilateral auditory deprivation showed miRNA changes in the IC. The contralateral IC showed decreased miRNA expression predicted to be related to MAPK and RAS signaling, whereas the ipsilateral IC revealed decreased miRNA expression predicted to be associated with synaptic plasticity and calcium ion transport.
单侧耳聋(SSD)后,下丘脑中存在去传入和代偿性神经可塑性变化。我们使用 miRNA 微阵列分析探讨了 SSD 大鼠下丘脑中相关的 miRNA 变化。
将 8 周龄大鼠分为对照组和 SSD 组(每组 n=8)。SSD 大鼠接受右侧耳蜗消融手术,术后两周采集下丘。使用 GeneChip miRNA 4.0 微阵列(Affymetrix Inc.)进行 miRNA 微阵列分析。使用定量逆转录聚合酶链反应(qRT-PCR)检测 SSD 大鼠与对照组相比表达水平变化倍数≥1.5且 P<0.05 的 miRNA。使用 TargetScan 软件预测差异表达 miRNA 的靶基因。分析与预测靶基因相关的途径。使用 qRT-PCR 估计预测靶基因的 mRNA 水平。
与对照组相比,SSD 大鼠对侧(左侧)IC 中 miR-15b-5p、miR-202-5p 和 miR-212-3p 的表达降低。SSD 大鼠对侧 IC 中 miR-15b-5p、miR-202-5p 和 miR-212-3p 的表达水平分别降低了 0.45、0.25 和 0.50 倍(P<0.05)。预测靶基因(Spred1、Rasa1、Lsm11 和 Srsf1)在 SSD 大鼠对侧 IC 中的表达高于对照组。预测这些靶基因与生长转录物终止区的切割、丝裂原激活蛋白激酶家族信号级联、RAF/AMP 激酶级联、GTP 酶激活蛋白(GAPs)对 RAS 的调节以及 RNA 聚合酶 II 转录终止有关。对于同侧 IC,miR-425-3p、miR-199a-5p 和 miR-134-3p 在 SSD 大鼠中的表达低于对照组,分别降低了 0.55、0.61 和 0.69 倍(P<0.05)。预测靶基因(Atp2b2、Grin2b、Foxp1、Ztbt20、Zfp91 和 Strn)在 SSD 大鼠同侧 IC 中的表达较高;这些靶基因可能与突触可塑性调节、cAMP 信号通路、金属离子结合和钙离子转运有关。
单侧听觉剥夺的成年大鼠在下丘脑中出现 miRNA 变化。对侧 IC 表现出降低的 miRNA 表达,预测与 MAPK 和 RAS 信号有关,而同侧 IC 则表现出降低的 miRNA 表达,预测与突触可塑性和钙离子转运有关。