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神经嵴的多能性与特化:单细胞转录组学方法的优势与局限

Neural crest multipotency and specification: power and limits of single cell transcriptomic approaches.

作者信息

Artinger Kristin B, Monsoro-Burq Anne H

机构信息

Department of Craniofacial Biology, University of Colorado School of Dental Medicine, Aurora, CO, USA.

Université Paris-Saclay, Faculté des Sciences d'Orsay, France.

出版信息

Fac Rev. 2021 Apr 14;10:38. doi: 10.12703/r/10-38. eCollection 2021.

Abstract

The neural crest is a unique population of multipotent cells forming in vertebrate embryos. Their vast cell fate potential enables the generation of a diverse array of differentiated cell types . These include, among others, connective tissue, cartilage and bone of the face and skull, neurons and glia of the peripheral nervous system (including enteric nervous system), and melanocytes. Following migration, these derivatives extensively populate multiple germ layers. Within the competent neural border ectoderm, an area located at the junction between the neural and non-neural ectoderm during embryonic development, neural crest cells form in response to a series of inductive secreted cues including BMP, Wnt, and FGF signals. As cells become progressively specified, they express transcriptional modules conducive with their stage of fate determination or cell state. Those sequential states include the neural border state, the premigratory neural crest state, the epithelium-to-mesenchyme transitional state, and the migratory state to end with post-migratory and differentiation states. However, despite the extensive knowledge accumulated over 150 years of neural crest biology, many key questions remain open, in particular the timing of neural crest lineage determination, the control of potency during early developmental stages, and the lineage relationships between different subpopulations of neural crest cells. In this review, we discuss the recent advances in understanding early neural crest formation using cutting-edge high-throughput single cell sequencing approaches. We will discuss how this new transcriptomic data, from 2017 to 2021, has advanced our knowledge of the steps in neural crest cell lineage commitment and specification, the mechanisms driving multipotency, and diversification. We will then discuss the questions that remain to be resolved and how these approaches may continue to unveil the biology of these fascinating cells.

摘要

神经嵴是脊椎动物胚胎中形成的一类独特的多能细胞群。它们巨大的细胞命运潜能能够产生各种各样分化的细胞类型。其中包括面部和颅骨的结缔组织、软骨和骨骼、外周神经系统(包括肠神经系统)的神经元和神经胶质细胞,以及黑素细胞。迁移后,这些衍生物广泛分布于多个胚层。在感受态神经边界外胚层内,即在胚胎发育过程中位于神经外胚层和非神经外胚层交界处的一个区域,神经嵴细胞在一系列诱导性分泌信号(包括骨形态发生蛋白、Wnt和FGF信号)的作用下形成。随着细胞逐渐特化,它们表达与命运决定阶段或细胞状态相适应的转录模块。这些连续的状态包括神经边界状态、迁移前神经嵴状态、上皮-间充质过渡状态和迁移状态,最终以迁移后和分化状态结束。然而,尽管在150多年的神经嵴生物学研究中积累了大量知识,但许多关键问题仍然悬而未决,特别是神经嵴谱系确定的时间、早期发育阶段潜能的控制,以及神经嵴细胞不同亚群之间的谱系关系。在这篇综述中,我们讨论了利用前沿的高通量单细胞测序方法在理解早期神经嵴形成方面的最新进展。我们将讨论从2017年到2021年的这些新的转录组数据如何推进了我们对神经嵴细胞谱系定向和特化步骤、驱动多能性和多样化的机制的认识。然后,我们将讨论仍有待解决的问题,以及这些方法如何可能继续揭示这些迷人细胞的生物学特性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8693/8130411/9b4b3b613535/facrev-10-38-g001.jpg

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