Qian Tianmei, Qiao Pingping, Lu Yingnan, Wang Hongkui
School of Biology and Basic Medical Sciences, Suzhou Medical College of Soochow University, Suzhou, China.
Key Laboratory of Neuroregeneration of Jiangsu and Ministry of Education, Co-Innovation Center of Neuroregeneration, NMPA Key Laboratory for Research and Evaluation of Tissue Engineering Technology Products, Nantong University, Nantong, China.
Front Vet Sci. 2022 Aug 15;9:936620. doi: 10.3389/fvets.2022.936620. eCollection 2022.
Transcription factors bind to specific DNA sequences, modulate the transcription of target genes, and regulate various biological processes, including peripheral nerve regeneration. Our previous analysis showed that SS18L1, a gene encoding the transcription factor SS18-like protein 1, was differentially expressed in the distal sciatic nerve stumps after rat sciatic nerve transection injury, but its effect on peripheral nerve injury has not been reported. In the current study, we isolated and cultured primary Schwann cells, and examined the role of SS18L1 for the biological functions of the cells. Depletion of SS18L1 by siRNA in Schwann cells enhanced cell proliferation and inhibited cell migration, as determined by EdU assay and transwell migration assay, respectively. In addition, silencing of SS18L1 inhibited Schwann cell differentiation induced by HRG and cAMP. Bioinformatics analyses revealed an interaction network of SS18L1, including DF2, SMARCD1, SMARCA4, and SMARCE1, which may be implicated in the regulatory functions of SS18L1 on the proliferation, migration and differentiation of Schwann cells. In conclusion, our results revealed a temporal expression profile of SS18L1 in peripheral nerve injury and its potential roles during the process of nerve recovery.
转录因子与特定的DNA序列结合,调节靶基因的转录,并调控包括周围神经再生在内的各种生物学过程。我们之前的分析表明,编码转录因子SS18样蛋白1的基因SS18L1在大鼠坐骨神经横断损伤后远端坐骨神经残端中差异表达,但其对周围神经损伤的影响尚未见报道。在本研究中,我们分离并培养了原代雪旺细胞,并研究了SS18L1对这些细胞生物学功能的作用。分别通过EdU检测和Transwell迁移检测确定,雪旺细胞中通过siRNA敲低SS18L1可增强细胞增殖并抑制细胞迁移。此外,沉默SS18L1可抑制由HRG和cAMP诱导的雪旺细胞分化。生物信息学分析揭示了一个包括DF2、SMARCD1、SMARCA4和SMARCE1的SS18L1相互作用网络,这可能与SS18L1对雪旺细胞增殖、迁移和分化的调控功能有关。总之,我们的结果揭示了SS18L1在周围神经损伤中的时间表达谱及其在神经恢复过程中的潜在作用。