Auditory Development and Restoration Program, National Institutes on Deafness and Other Communication Disorders, National Institutes of Health, Porter Neuroscience Research Center, 35 Convent Dr., Room 1F-226, Bethesda, MD, 20892, USA.
Biomedical Research Informatics Office, National Institute of Dental and Craniofacial Research, NIH, Bethesda, MD, 20892, USA.
Sci Rep. 2020 Oct 22;10(1):18100. doi: 10.1038/s41598-020-75238-8.
The stria vascularis (SV) in the cochlea generates and maintains the endocochlear potential, thereby playing a pivotal role in normal hearing. Knowing transcriptional profiles and gene regulatory networks of SV cell types establishes a basis for studying the mechanism underlying SV-related hearing loss. While we have previously characterized the expression profiles of major SV cell types in the adult mouse, transcriptional profiles of rare SV cell types remained elusive due to the limitation of cell capture in single-cell RNA-Seq. The role of these rare cell types in the homeostatic function of the adult SV remain largely undefined. In this study, we performed single-nucleus RNA-Seq on the adult mouse SV in conjunction with sample preservation treatments during the isolation steps. We distinguish rare SV cell types, including spindle cells and root cells, from other cell types, and characterize their transcriptional profiles. Furthermore, we also identify and validate novel specific markers for these rare SV cell types. Finally, we identify homeostatic gene regulatory networks within spindle and root cells, establishing a basis for understanding the functional roles of these cells in hearing. These novel findings will provide new insights for future work in SV-related hearing loss and hearing fluctuation.
血管纹(SV)在耳蜗中产生和维持内淋巴电位,从而在正常听力中发挥关键作用。了解 SV 细胞类型的转录谱和基因调控网络为研究 SV 相关听力损失的机制奠定了基础。虽然我们之前已经描述了成年小鼠中主要 SV 细胞类型的表达谱,但由于单细胞 RNA-Seq 中细胞捕获的限制,稀有 SV 细胞类型的转录谱仍然难以捉摸。这些稀有细胞类型在成年 SV 的稳态功能中的作用在很大程度上仍未得到定义。在这项研究中,我们对成年小鼠 SV 进行了单核 RNA-Seq 分析,并在分离步骤中结合了样本保存处理。我们将稀有 SV 细胞类型(包括纺锤形细胞和根细胞)与其他细胞类型区分开来,并描述了它们的转录谱。此外,我们还鉴定和验证了这些稀有 SV 细胞类型的新型特异性标记物。最后,我们确定了纺锤形和根细胞内的稳态基因调控网络,为理解这些细胞在听力中的功能作用奠定了基础。这些新发现将为未来与 SV 相关的听力损失和听力波动的研究提供新的见解。