Henrique Domingos, Abranches Elsa, Verrier Laure, Storey Kate G
Instituto de Medicina Molecular and Instituto de Histologia e Biologia do Desenvolvimento, Faculdade de Medicina da Universidade de Lisboa, Avenida Prof. Egas Moniz, Lisboa 1649-028, Portugal.
Division of Cell & Developmental Biology, College of Life Sciences, University of Dundee, Dow Street, Dundee DD1 5EH, UK.
Development. 2015 Sep 1;142(17):2864-75. doi: 10.1242/dev.119768.
Neuromesodermal progenitors (NMps) contribute to both the elongating spinal cord and the adjacent paraxial mesoderm. It has been assumed that these cells arise as a result of patterning of the anterior neural plate. However, as the molecular mechanisms that specify NMps in vivo are uncovered, and as protocols for generating these bipotent cells from mouse and human pluripotent stem cells in vitro are established, the emerging data suggest that this view needs to be revised. Here, we review the characteristics, regulation, in vitro derivation and in vivo induction of NMps. We propose that these cells arise within primitive streak-associated epiblast via a mechanism that is separable from that which establishes neural fate in the anterior epiblast. We thus argue for the existence of two distinct routes for making central nervous system progenitors.
神经中胚层祖细胞(NMps)对脊髓的延伸和相邻的轴旁中胚层都有贡献。一直以来人们认为这些细胞是前神经板模式化的结果。然而,随着体内确定NMps的分子机制被揭示,以及从小鼠和人类多能干细胞体外生成这些双能细胞的方案得以确立,新出现的数据表明这一观点需要修正。在这里,我们综述了NMps的特征、调控、体外衍生和体内诱导。我们提出这些细胞通过一种与在前外胚层建立神经命运的机制可分离的机制,在与原条相关的外胚层内产生。因此,我们认为存在两种不同的途径来产生中枢神经系统祖细胞。