Chadly Duncan M, Best Jennifer, Ran Cong, Bruska Małgorzata, Woźniak Witold, Kempisty Bartosz, Schwartz Mark, LaFleur Bonnie, Kerns B J, Kessler John A, Matsuoka Akihiro J
Department of Otolaryngology and Head and Neck Surgery, Feinberg School of Medicine, Northwestern University, Chicago, Illinois, United States of America.
Department of Anatomy, Poznań University, Poznań, Poland.
PLoS One. 2018 Jan 26;13(1):e0191452. doi: 10.1371/journal.pone.0191452. eCollection 2018.
Due to the extreme inaccessibility of fetal human inner ear tissue, defining of the microRNAs (miRNAs) that regulate development of the inner ear has relied on animal tissue. In the present study, we performed the first miRNA sequencing of otic precursors in human specimens. Using HTG miRNA Whole Transcriptome assays, we examined miRNA expression in the cochleovestibular ganglion (CVG), neural crest (NC), and otic vesicle (OV) from paraffin embedded (FFPE) human specimens in the Carnegie developmental stages 13-15. We found that in human embryonic tissues, there are different patterns of miRNA expression in the CVG, NC and OV. In particular, members of the miR-183 family (miR-96, miR-182, and miR-183) are differentially expressed in the CVG compared to NC and OV at Carnegie developmental stage 13. We further identified transcription factors that are differentially targeted in the CVG compared to the other tissues from stages 13-15, and we performed gene set enrichment analyses to determine differentially regulated pathways that are relevant to CVG development in humans. These findings not only provide insight into the mechanisms governing the development of the human inner ear, but also identify potential signaling pathways for promoting regeneration of the spiral ganglion and other components of the inner ear.
由于胎儿人类内耳组织极难获取,确定调控内耳发育的微小RNA(miRNA)一直依赖于动物组织。在本研究中,我们首次对人类标本中的耳前体细胞进行了miRNA测序。使用HTG miRNA全转录组分析方法,我们检测了卡内基发育阶段13 - 15的石蜡包埋(FFPE)人类标本中,耳蜗前庭神经节(CVG)、神经嵴(NC)和耳泡(OV)中的miRNA表达。我们发现,在人类胚胎组织中,CVG、NC和OV中的miRNA表达模式各不相同。特别是,在卡内基发育阶段13时,与NC和OV相比,miR - 183家族成员(miR - 96、miR - 182和miR - 183)在CVG中差异表达。我们进一步确定了在13 - 15阶段与其他组织相比,CVG中差异靶向的转录因子,并进行了基因集富集分析,以确定与人类CVG发育相关的差异调控途径。这些发现不仅为人类内耳发育的调控机制提供了见解,还确定了促进螺旋神经节及内耳其他成分再生的潜在信号通路。