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单细胞分析揭示了人视网膜发育过程中睫状缘的短暂视网膜祖细胞。

Single-cell analyses reveal transient retinal progenitor cells in the ciliary margin of developing human retina.

机构信息

Biosciences Institute, Newcastle University, Newcastle, UK.

Department of Biotechnological and Applied Clinical Sciences, University of L'Aquila, L'Aquila, Italy.

出版信息

Nat Commun. 2024 Apr 26;15(1):3567. doi: 10.1038/s41467-024-47933-x.

Abstract

The emergence of retinal progenitor cells and differentiation to various retinal cell types represent fundamental processes during retinal development. Herein, we provide a comprehensive single cell characterisation of transcriptional and chromatin accessibility changes that underline retinal progenitor cell specification and differentiation over the course of human retinal development up to midgestation. Our lineage trajectory data demonstrate the presence of early retinal progenitors, which transit to late, and further to transient neurogenic progenitors, that give rise to all the retinal neurons. Combining single cell RNA-Seq with spatial transcriptomics of early eye samples, we demonstrate the transient presence of early retinal progenitors in the ciliary margin zone with decreasing occurrence from 8 post-conception week of human development. In retinal progenitor cells, we identified a significant enrichment for transcriptional enhanced associate domain transcription factor binding motifs, which when inhibited led to loss of cycling progenitors and retinal identity in pluripotent stem cell derived organoids.

摘要

视网膜祖细胞的出现和向各种视网膜细胞类型的分化是视网膜发育过程中的基本过程。在这里,我们提供了一个全面的单细胞特征描述,说明了在人类视网膜发育过程中,从妊娠中期到中期,转录和染色质可及性变化是如何强调视网膜祖细胞的特化和分化的。我们的谱系轨迹数据表明存在早期视网膜祖细胞,它们向晚期和进一步向短暂的神经发生祖细胞过渡,这些祖细胞产生所有的视网膜神经元。将单细胞 RNA-Seq 与早期眼样本的空间转录组学相结合,我们证明了早期视网膜祖细胞在睫状缘区的短暂存在,从人类发育的 8 个受孕后周开始,其出现的频率逐渐降低。在视网膜祖细胞中,我们发现转录增强相关域转录因子结合基序显著富集,当抑制这些基序时,会导致多能干细胞衍生的类器官中循环祖细胞和视网膜特性的丧失。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1a9b/11053058/a3892251080b/41467_2024_47933_Fig1_HTML.jpg

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