Díaz Carmen, Morales-Delgado Nicanor, Puelles Luis
Department of Medical Sciences, School of Medicine and Institute for Research in Neurological Disabilities, University of Castilla-La Mancha Albacete, Spain.
Department of Human Anatomy and Psychobiology, University of Murcia, School of Medicine and IMIB (Instituto Murciano de Investigación Biosanitaria) Murcia, Spain.
Front Neuroanat. 2015 Jan 12;8:162. doi: 10.3389/fnana.2014.00162. eCollection 2014.
During early development, the hypothalamic primordium undergoes anteroposterior and dorsoventral regionalization into diverse progenitor domains, each characterized by a differential gene expression code. The types of neurons produced selectively in each of these distinct progenitor domains are still poorly understood. Recent analysis of the ontogeny of peptidergic neuronal populations expressing Sst, Ghrh, Crh and Trh mRNAs in the mouse hypothalamus showed that these cell types originate from particular dorsoventral domains, characterized by specific combinations of gene markers. Such analysis implies that the differentiation of diverse peptidergic cell populations depends on the molecular environment where they are born. Moreover, a number of these peptidergic neurons were observed to migrate radially and/or tangentially, invading different adult locations, often intermingled with other cell types. This suggests that a developmental approach is absolutely necessary for the understanding of their adult distribution. In this essay, we examine comparatively the ontogenetic hypothalamic topography of twelve additional peptidergic populations documented in the Allen Developmental Mouse Brain Atlas, and discuss shared vs. variant aspects in their apparent origins, migrations and final distribution, in the context of the respective genoarchitectonic backgrounds. This analysis should aid ulterior attempts to explain causally the development of neuronal diversity in the hypothalamus, and contribute to our understanding of its topographic complexity in the adult.
在早期发育过程中,下丘脑原基经历前后和背腹区域化,形成不同的祖细胞区域,每个区域都有不同的基因表达编码特征。在这些不同的祖细胞区域中选择性产生的神经元类型仍知之甚少。最近对小鼠下丘脑中表达Sst、Ghrh、Crh和Trh mRNA的肽能神经元群体个体发生的分析表明,这些细胞类型起源于特定的背腹区域,其特征是基因标记的特定组合。这种分析意味着不同肽能细胞群体的分化取决于它们产生时的分子环境。此外,观察到许多这些肽能神经元沿径向和/或切向迁移,侵入不同的成年位置,常常与其他细胞类型混合在一起。这表明,采用发育学方法对于理解它们在成年期的分布绝对必要。在本文中,我们比较研究了《艾伦发育小鼠脑图谱》中记录的另外12个肽能群体的下丘脑个体发生拓扑结构,并在各自的基因结构背景下,讨论它们在明显起源、迁移和最终分布方面的共性和差异。这种分析应有助于进一步尝试因果性地解释下丘脑中神经元多样性的发育,并有助于我们理解其在成年期的拓扑复杂性。