Suppr超能文献

单细胞转录组分析揭示了具有潜力的青光眼神经修复基因。

Single-cell transcriptome analysis of regenerating RGCs reveals potent glaucoma neural repair genes.

机构信息

Spencer Center for Vision Research, Department of Ophthalmology, Byers Eye Institute at Stanford University School of Medicine, Palo Alto, CA 94304, USA.

Spencer Center for Vision Research, Department of Ophthalmology, Byers Eye Institute at Stanford University School of Medicine, Palo Alto, CA 94304, USA; Department of Ophthalmology, The Second Xiangya Hospital, Central South University, Changsha 410011, China.

出版信息

Neuron. 2022 Aug 17;110(16):2646-2663.e6. doi: 10.1016/j.neuron.2022.06.022. Epub 2022 Aug 10.

Abstract

Axon regeneration holds great promise for neural repair of CNS axonopathies, including glaucoma. Pten deletion in retinal ganglion cells (RGCs) promotes potent optic nerve regeneration, but only a small population of Pten-null RGCs are actually regenerating RGCs (regRGCs); most surviving RGCs (surRGCs) remain non-regenerative. Here, we developed a strategy to specifically label and purify regRGCs and surRGCs, respectively, from the same Pten-deletion mice after optic nerve crush, in which they differ only in their regeneration capability. Smart-Seq2 single-cell transcriptome analysis revealed novel regeneration-associated genes that significantly promote axon regeneration. The most potent of these, Anxa2, acts synergistically with its ligand tPA in Pten-deletion-induced axon regeneration. Anxa2, its downstream effector ILK, and Mpp1 dramatically protect RGC somata and axons and preserve visual function in a clinically relevant model of glaucoma, demonstrating the exciting potential of this innovative strategy to identify novel effective neural repair candidates.

摘要

轴突再生为中枢神经系统轴突病(包括青光眼)的神经修复带来了巨大的希望。视网膜神经节细胞(RGCs)中的 Pten 缺失可促进强有力的视神经再生,但只有一小部分 Pten 缺失的 RGCs 实际上是再生的 RGCs(regRGCs);大多数存活的 RGCs(surRGCs)仍然是不可再生的。在这里,我们开发了一种策略,即在视神经挤压后,从相同的 Pten 缺失小鼠中分别特异性标记和纯化 regRGCs 和 surRGCs,它们仅在再生能力上有所不同。Smart-Seq2 单细胞转录组分析揭示了新的与再生相关的基因,这些基因显著促进了轴突的再生。其中最有效的是 Anxa2,它与其配体 tPA 在 Pten 缺失诱导的轴突再生中协同作用。Anxa2、其下游效应物 ILK 和 Mpp1 可显著保护 RGC 体和轴突,并在青光眼的临床相关模型中保留视觉功能,这表明这种创新策略具有令人兴奋的潜力,可以鉴定新的有效的神经修复候选物。

相似文献

引用本文的文献

1
Cutting-edge technologies in neural regeneration.神经再生领域的前沿技术。
Cell Regen. 2025 Sep 5;14(1):38. doi: 10.1186/s13619-025-00260-y.

本文引用的文献

9
Integrated analysis of multimodal single-cell data.多模态单细胞数据的综合分析。
Cell. 2021 Jun 24;184(13):3573-3587.e29. doi: 10.1016/j.cell.2021.04.048. Epub 2021 May 31.

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验