Weston James A, Thiery Jean Paul
Institute of Neuroscience, University of Oregon, Eugene, OR, USA.
Institute of Molecular and Cell Biology, A(⁎)STAR, Proteos, Singapore; Cancer Science Institute, National University of Singapore, Singapore; Department of Biochemistry, Yong Loo Lin School of Medicine, National University of Singapore, Singapore.
Dev Biol. 2015 May 1;401(1):37-61. doi: 10.1016/j.ydbio.2014.12.035. Epub 2015 Jan 15.
The Neural Crest, a transient epithelium in vertebrate embryos, is the source of putative stem cells known to give rise to neuronal, glial and endocrine components of the peripheral (sensory, autonomic and enteric) nervous system (PNS) and pigment cells in the skin. The Neural Crest is also widely believed to be the source of mesectodermal derivatives (skeletogenic, odontogenic, connective tissue and smooth muscle mesenchyme) in the vertebrate head [see (Bronner and LeDouarin, 2012; Le Douarin, 2012; Le Douarin and Kalcheim, 1999); see also (Hörstadius, 1950; Weston, 1970)]. This conventional understanding of the broad developmental potential of the Neural Crest has been challenged over the past few years (Breau et al., 2008; Lee et al., 2013a, 2013b; Weston et al., 2004), based on recognition that the definition of the embryonic epithelia that comprise the Neural Crest may be imprecise. Indeed, the definition of the embryonic tissues understood to constitute the Neural Crest has changed considerably since it was first described by Wilhelm His 150 years ago (His, 1868). Today, the operational definition of the Neural Crest is inconsistent and functionally ambiguous. We believe that more precise definitions of the embryonic tissues involved in Neural Crest development would be useful to understand (1) the range of cellular phenotypes that actually segregate from it, (2) when this lineage diversification occurs, and (3) how diversification is regulated. In this idiosyncratic review, we aim to explain our concerns with the current definitions in this field, and in the chiastic words of Samuel Johnson (1781), "… make new things familiar and familiar things new".(1) Then, we will try to distinguish the developmental events crucial to the regulation of Neural Crest development at both cranial and trunk axial levels of vertebrate embryos, and address some of the implicit assumptions that underlie the conventional interpretation of experimental results on the origin and fates of Neural Crest-derived cells. We hope our discussion will resolve some ambiguities regarding both the range of derivatives in the Neural Crest lineage and the conventional understanding that cranial mesectodermal derivatives share a common Neural Crest-derived lineage precursor with components of the PNS.
神经嵴是脊椎动物胚胎中的一种短暂上皮组织,是已知的假定干细胞来源,可产生外周(感觉、自主和肠)神经系统(PNS)的神经元、神经胶质和内分泌成分以及皮肤中的色素细胞。人们还普遍认为神经嵴是脊椎动物头部中胚层衍生物(骨骼生成、牙齿生成、结缔组织和平滑肌间充质)的来源[见(Bronner和LeDouarin,2012年;Le Douarin,2012年;Le Douarin和Kalcheim,1999年);另见(Hörstadius,1950年;Weston,1970年)]。在过去几年中,这种对神经嵴广泛发育潜能的传统理解受到了挑战(Breau等人,2008年;Lee等人,2013a、2013b;Weston等人,2004年),这是基于认识到构成神经嵴的胚胎上皮组织的定义可能不准确。事实上,自150年前由Wilhelm His首次描述以来,被认为构成神经嵴的胚胎组织的定义已经发生了很大变化(His,1868年)。如今,神经嵴的操作定义不一致且功能模糊。我们认为,对参与神经嵴发育的胚胎组织进行更精确的定义,将有助于理解:(1)实际从其分离的细胞表型范围;(2)这种谱系多样化何时发生;(3)多样化是如何被调控的。在这篇别具一格的综述中,我们旨在解释我们对该领域当前定义的担忧,并用塞缪尔·约翰逊(1781年)的话来说就是“……让新事物变得熟悉,让熟悉的事物变得新颖”。(1)然后,我们将尝试区分在脊椎动物胚胎的头部和躯干轴水平上对神经嵴发育调控至关重要的发育事件,并探讨一些传统上对神经嵴衍生细胞的起源和命运实验结果解释所依据的隐含假设。我们希望我们的讨论能够解决关于神经嵴谱系中衍生物范围以及颅中胚层衍生物与PNS成分共享共同的神经嵴衍生谱系前体这一传统理解方面的一些模糊之处。