Transcriptome analysis of molecular mechanisms underlying facial nerve injury repair in rats

Qian-Qian Cao; Shuo Li; Yan Lu; Di Wu; Wei Feng; Yong Shi; Lu-Ping Zhang

doi:10.4103/1673-5374.310700

Transcriptome analysis of molecular mechanisms underlying facial nerve injury repair in rats

Neural Regen Res. 2021 Nov;16(11):2316-2323. doi: 10.4103/1673-5374.310700.

Authors

Qian-Qian Cao¹, Shuo Li², Yan Lu¹, Di Wu², Wei Feng¹, Yong Shi³, Lu-Ping Zhang²

Affiliations

¹ Key Laboratory of Neuroregeneration of Jiangsu and Ministry of Education, Co-innovation Center of Neuroregeneration, Nantong University, Nantong, Jiangsu Province, China.
² Department of Otolaryngology, Affiliated Hospital of Nantong University, Nantong, Jiangsu Province, China.
³ Department of Otolaryngology, Head and Neck Surgery, Eye, Ear, Nose and Throat Hospital, Fudan University, Shanghai, China.

Abstract

Although the transcriptional alterations inside the facial nucleus after facial nerve injury have been well studied, the gene expression changes in the facial nerve trunk after injury are still unknown. In this study, we established an adult rat model of facial nerve crush injury by compressing the right lateral extracranial nerve trunk. Transcriptome sequencing, differential gene expression analysis, and cluster analysis of the injured facial nerve trunk were performed, and 39 intersecting genes with significant variance in expression were identified. Gene Ontology annotation and Kyoto Encyclopedia of Genes and Genomes pathway analyses of the 39 intersecting genes revealed that these genes are mostly involved in leukocyte cell-cell adhesion and phagocytosis and have essential roles in regulating nerve repair. Quantitative real-time polymerase chain reaction assays were used to validate the expression of pivotal genes. Finally, nine pivotal genes that contribute to facial nerve recovery were identified, including Arhgap30, Akr1b8, C5ar1, Csf2ra, Dock2, Hcls1, Inpp5d, Sla, and Spi1. Primary Schwann cells were isolated from the sciatic nerve of neonatal rats. After knocking down Akr1b8 in Schwann cells with an Akr1b8-specific small interfering RNA plasmid, expression levels of monocyte chemoattractant protein-1 and interleukin-6 were decreased, while cell proliferation and migration were not obviously altered. These findings suggest that Akr1b8 likely regulates the interaction between Schwann cells and macrophages through regulation of cytokine expression to promote facial nerve regeneration. This study is the first to reveal a transcriptome change in the facial nerve trunk after facial nerve injury, thereby revealing the potential mechanism underlying repair of facial nerve injury. This study was approved by the Animal Ethics Committee of Nantong University, China in 2018 (approval No. S20180923-007).

Keywords: Akr1b8; Gene-Act Networks; RNA-Seq; Schwann cells; cell proliferation; facial nerve injury; inflammatory response; transcriptomics analysis.