Dietz André, Senf Katja, Neuhaus Eva M
Pharmacology and Toxicology, Jena University Hospital, Friedrich Schiller University Jena, Drackendorfer Str. 1, 07747 Jena, Germany.
J Cell Sci. 2025 Jan 1;138(1). doi: 10.1242/jcs.263451. Epub 2025 Jan 9.
The vomeronasal organ (VNO) detects signaling molecules that often prompt innate behaviors, such as aggression and reproduction. Vomeronasal sensory neurons, classified into apical and basal lineages based on receptor expression, have a limited lifespan and are continuously replaced from a common stem cell niche. Using a combination of single-cell RNA sequencing data, immunofluorescence staining and lineage tracing, we identified CXCR4 expression in proliferative stem cells and the basal neuronal lineage. Mice with a conditional knockout of Cxcr4 showed an increased number of SOX2-positive proliferative stem cells and enhanced basal neuronal lineage maturation. In addition, computational gene perturbation analysis revealed 87 transcription factors that might contribute to neurogenesis, among which was SOX2. Conditional knockout of Cxcr4 did not only disturb neuronal maturation, but also affected non-neuronal cell types, resulting in a decrease of basal lamina lining quiescent stem cells and an increase in sustentacular support cells. Together, these findings enhance our understanding how a common pool of stem cells can give rise to different cell types of the VNO, highlighting the distinct role of CXCR4 in this process.
犁鼻器(VNO)可检测常常引发诸如攻击和繁殖等先天行为的信号分子。根据受体表达分为顶端和基底谱系的犁鼻器感觉神经元寿命有限,并不断从一个共同的干细胞生态位得到补充。通过结合单细胞RNA测序数据、免疫荧光染色和谱系追踪,我们在增殖性干细胞和基底神经元谱系中鉴定出了CXCR4的表达。条件性敲除Cxcr4的小鼠显示SOX2阳性增殖性干细胞数量增加,基底神经元谱系成熟增强。此外,计算基因扰动分析揭示了87个可能有助于神经发生的转录因子,其中包括SOX2。条件性敲除Cxcr4不仅扰乱神经元成熟,还影响非神经元细胞类型,导致衬于静止干细胞的基膜减少,支持细胞增多。总之,这些发现增进了我们对一个共同的干细胞库如何产生犁鼻器不同细胞类型的理解,突出了CXCR4在此过程中的独特作用。