Jing Junzhan, Hu Ming, Ngodup Tenzin, Ma Qianqian, Lau Shu-Ning Natalie, Ljungberg Cecilia, McGinley Matthew J, Trussell Laurence O, Jiang Xiaolong
Jan and Dan Duncan Neurological Research Institute at Texas Children's Hospital, Houston, TX,USA.
Department of Neuroscience, Baylor College of Medicine, Houston, TX, USA.
bioRxiv. 2024 Oct 6:2023.05.15.539065. doi: 10.1101/2023.05.15.539065.
The cochlear nuclear complex (CN), the starting point for all central auditory processing, comprises a suite of neuronal cell types that are highly specialized for neural coding of acoustic signals, yet molecular logic governing cellular specializations remains unknown. By combining single-nucleus RNA sequencing and Patch-seq analysis, we reveal a set of transcriptionally distinct cell populations encompassing all previously observed types and discover multiple new subtypes with anatomical and physiological identity. The resulting comprehensive cell-type taxonomy reconciles anatomical position, morphological, physiological, and molecular criteria, enabling the determination of the molecular basis of the remarkable cellular phenotypes in the CN. In particular, CN cell-type identity is encoded in a transcriptional architecture that orchestrates functionally congruent expression across a small set of gene families to customize projection patterns, input-output synaptic communication, and biophysical features required for encoding distinct aspects of acoustic signals. This high-resolution account of cellular heterogeneity from the molecular to the circuit level illustrates molecular logic for cellular specializations and enables genetic dissection of auditory processing and hearing disorders with unprecedented specificity.
耳蜗核复合体(CN)是所有中枢听觉处理的起点,由一系列高度专门用于对声信号进行神经编码的神经元细胞类型组成,但控制细胞特化的分子逻辑仍然未知。通过结合单核RNA测序和膜片钳测序分析,我们揭示了一组转录上不同的细胞群体,涵盖了所有先前观察到的类型,并发现了多个具有解剖学和生理学特征的新亚型。由此产生的全面细胞类型分类法整合了解剖位置、形态、生理和分子标准,从而能够确定CN中显著细胞表型的分子基础。特别是,CN细胞类型的身份编码在一种转录结构中,该结构协调一小部分基因家族的功能一致表达,以定制投射模式、输入-输出突触通信以及编码声信号不同方面所需的生物物理特征。这种从分子到回路水平的细胞异质性的高分辨率描述阐明了细胞特化的分子逻辑,并以前所未有的特异性实现了对听觉处理和听力障碍的基因剖析。