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本文引用的文献

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From head to tail: regionalization of the neural crest.从头至尾:神经嵴的区域性。
Development. 2020 Oct 26;147(20):dev193888. doi: 10.1242/dev.193888.
2
Endogenous CRISPR/Cas9 arrays for scalable whole-organism lineage tracing.内源性 CRISPR/Cas9 阵列可用于可扩展的全生物体谱系追踪。
Development. 2020 May 12;147(9):dev184481. doi: 10.1242/dev.184481.
3
Reprogramming Axial Level Identity to Rescue Neural-Crest-Related Congenital Heart Defects.重编程轴向水平身份以挽救神经嵴相关先天性心脏缺陷。
Dev Cell. 2020 May 4;53(3):300-315.e4. doi: 10.1016/j.devcel.2020.04.005.
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DNA Barcoding in Nonhuman Primates Reveals Important Limitations in Retrovirus Integration Site Analysis.非人灵长类动物中的DNA条形码揭示了逆转录病毒整合位点分析中的重要局限性。
Mol Ther Methods Clin Dev. 2020 Mar 30;17:796-809. doi: 10.1016/j.omtm.2020.03.021. eCollection 2020 Jun 12.
5
In Vivo Lineage Tracing of Polyploid Hepatocytes Reveals Extensive Proliferation during Liver Regeneration.体内多倍体肝细胞谱系追踪揭示了肝再生过程中的广泛增殖。
Cell Stem Cell. 2020 Jan 2;26(1):34-47.e3. doi: 10.1016/j.stem.2019.11.014. Epub 2019 Dec 19.
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In situ readout of DNA barcodes and single base edits facilitated by in vitro transcription.通过体外转录实现 DNA 条码和单碱基编辑的原位读出。
Nat Biotechnol. 2020 Jan;38(1):66-75. doi: 10.1038/s41587-019-0299-4. Epub 2019 Nov 18.
7
Evolution of the new head by gradual acquisition of neural crest regulatory circuits.新头的进化是通过逐渐获得神经嵴调控回路实现的。
Nature. 2019 Oct;574(7780):675-678. doi: 10.1038/s41586-019-1691-4. Epub 2019 Oct 23.
8
Adult sox10 Cardiomyocytes Contribute to Myocardial Regeneration in the Zebrafish.成年 sox10 心肌细胞有助于斑马鱼的心肌再生。
Cell Rep. 2019 Oct 22;29(4):1041-1054.e5. doi: 10.1016/j.celrep.2019.09.041.
9
Cardiac neural crest contributes to cardiomyocytes in amniotes and heart regeneration in zebrafish.心脏神经嵴为羊膜动物的心肌细胞和斑马鱼的心脏再生做出贡献。
Elife. 2019 Aug 8;8:e47929. doi: 10.7554/eLife.47929.
10
Schwann cell precursors contribute to skeletal formation during embryonic development in mice and zebrafish.许旺细胞前体细胞在胚胎发育过程中有助于骨骼形成,无论是在小鼠还是斑马鱼中。
Proc Natl Acad Sci U S A. 2019 Jul 23;116(30):15068-15073. doi: 10.1073/pnas.1900038116. Epub 2019 Jul 8.

神经嵴谱系分析:从过去到未来轨迹。

Neural crest lineage analysis: from past to future trajectory.

机构信息

Division of Biology and Biological Engineering, California Institute of Technology, Pasadena, CA 91125, USA.

Division of Biology and Biological Engineering, California Institute of Technology, Pasadena, CA 91125, USA

出版信息

Development. 2020 Oct 23;147(20):dev193193. doi: 10.1242/dev.193193.

DOI:10.1242/dev.193193
PMID:33097550
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7595686/
Abstract

Since its discovery 150 years ago, the neural crest has intrigued investigators owing to its remarkable developmental potential and extensive migratory ability. Cell lineage analysis has been an essential tool for exploring neural crest cell fate and migration routes. By marking progenitor cells, one can observe their subsequent locations and the cell types into which they differentiate. Here, we review major discoveries in neural crest lineage tracing from a historical perspective. We discuss how advancing technologies have refined lineage-tracing studies, and how clonal analysis can be applied to questions regarding multipotency. We also highlight how effective progenitor cell tracing, when combined with recently developed molecular and imaging tools, such as single-cell transcriptomics, single-molecule fluorescence hybridization and high-resolution imaging, can extend the scope of neural crest lineage studies beyond development to regeneration and cancer initiation.

摘要

自 150 年前被发现以来,神经嵴因其显著的发育潜力和广泛的迁移能力而引起了研究人员的兴趣。细胞谱系分析一直是探索神经嵴细胞命运和迁移途径的重要工具。通过标记祖细胞,可以观察它们随后的位置以及它们分化成的细胞类型。在这里,我们从历史的角度回顾了神经嵴谱系追踪的主要发现。我们讨论了先进技术如何改进谱系追踪研究,以及克隆分析如何应用于关于多能性的问题。我们还强调了有效的祖细胞追踪,当与最近开发的分子和成像工具(如单细胞转录组学、单分子荧光杂交和高分辨率成像)结合使用时,如何将神经嵴谱系研究的范围从发育扩展到再生和癌症起始。