单细胞转录组学和表观基因组学分析揭示了嗅觉干细胞的潜在激活状态。

Koen Van den Berge, Dana Bakalar, Hsin-Jung Chou, Divya Kunda, Davide Risso, Kelly Street, Elizabeth Purdom, Sandrine Dudoit, John Ngai, Whitney Heavner
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引用次数: 0

摘要

嗅觉上皮是神经系统中维持神经发生的少数区域之一。它的实验可及性使其特别易于用于研究损伤诱导细胞死亡后驱动神经再生的分子机制。在这项研究中,我们使用单细胞测序来确定在急性损伤后决定嗅觉上皮干细胞命运的主要调控因子。我们结合基因表达和单个谱系追踪嗅觉干细胞的可接近染色质谱来预测不同谱系和恢复阶段特异性的转录因子活性。我们进一步确定了一种离散的干细胞状态,这种状态似乎处于激活状态,其特征是伤口反应周围可接近的染色质和谱系特异性基因,这些基因随后在损伤反应中表达。总之,这些结果提供了证据,表明静息嗅觉上皮干细胞亚群在表观遗传学上支持损伤诱导的再生。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
A Latent Activated Olfactory Stem Cell State Revealed by Single-Cell Transcriptomic and Epigenomic Profiling.

The olfactory epithelium is one of the few regions of the nervous system that sustains neurogenesis throughout life. Its experimental accessibility makes it especially tractable for studying molecular mechanisms that drive neural regeneration in response to injury. In this study, we used single-cell sequencing to identify the transcriptional cascades and epigenetic processes involved in determining olfactory epithelial stem cell fate during injury-induced regeneration. By combining gene expression and accessible chromatin profiles of individual lineage-traced olfactory stem cells, we identified transcriptional heterogeneity among activated stem cells at a stage when cell fates are being specified. We further identified a subset of resting cells that appears poised for activation, characterized by accessible chromatin around wound response and lineage-specific genes prior to their later expression in response to injury. Together these results provide evidence for a latent activated stem cell state, in which a subset of quiescent olfactory epithelial stem cells are epigenetically primed to support injury-induced regeneration.

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