Zhang Yuanfeng, Alvarez-Bolado Gonzalo
Department of Neuroanatomy, Institute of Anatomy and Cell Biology, University of Heidelberg, Heidelberg D-69120 Germany.
Department of Neuroanatomy, Institute of Anatomy and Cell Biology, University of Heidelberg, Heidelberg D-69120 Germany.
J Chem Neuroanat. 2016 Sep;75(Pt A):20-7. doi: 10.1016/j.jchemneu.2015.11.008. Epub 2015 Dec 12.
The traditional concept of diencephalon (thalamus plus hypothalamus) and with it the entire traditional subdivision of the developing neural tube are being challenged by novel insights obtained by mapping the expression of key developmental genes. A model in which the hypothalamus is placed in the most rostral portion of the neural tube, followed caudally by a diencephalon formed by prethalamus, thalamus and pretectum has been proposed. The adult thalamus and hypothalamus are quite unlike each other in connectivity and functions. Here we review work on the role of the secreted morphogen protein Sonic hedgehog (Shh) in the developing diencephalon and hypothalamic region to show how different these two regions are also from this point of view. Shh from the prechordal plate (PCP) induces and patterns the hypothalamus but there is no evidence that this role is fulfilled by a morphogen gradient. Later, the hypothalamic primordium itself expresses Shh and a large part of the hypothalamus belongs to the Shh lineage, including the ventral domains. Neural Shh is necessary to complete the specification (lateral hypothalamus), differentiation and growth of the hypothalamus. Although Gli2A is the major effector of Shh in this region, hypothalamic specification also depends on the suppression of Gli3R by Shh secreted by the PCP as well as the neuroepithelium. The thalamus is patterned by an Shh morphogen gradient originated in the ZLI following similar mechanisms to those in the spinal cord. The thalamus itself does not belong to the Shh lineage. Gli2A is necessary for appropriate growth and specification of the thalamic nuclei, to the exception of the medial and intralaminar groups (limbic-related), whose development depends on Gli3R. Beyond specification and patterning, the scarce data available about cell sorting and aggregation in these two regions shows key differences between them as well. In summary, not only expression patterns but also developmental mechanisms support a separation of the traditional thalamus and hypothalamus into different prosomeric domains.
传统的间脑概念(丘脑加下丘脑)以及与之相关的发育中神经管的整个传统细分,正受到通过绘制关键发育基因表达图谱所获得的新见解的挑战。有人提出了一种模型,其中下丘脑位于神经管的最前端部分,其后是由前丘脑、丘脑和顶盖前区形成的间脑。成年丘脑和下丘脑在连接性和功能上彼此截然不同。在这里,我们回顾了分泌型形态发生蛋白音猬因子(Shh)在间脑和下丘脑区域发育中的作用,以说明从这一角度来看这两个区域也是多么不同。来自脊索前板(PCP)的Shh诱导下丘脑并使其形成模式,但没有证据表明这种作用是由形态发生素梯度实现的。后来,下丘脑原基本身表达Shh,并且下丘脑的很大一部分属于Shh谱系,包括腹侧区域。神经Shh对于完成下丘脑的特化(外侧下丘脑)、分化和生长是必需的。尽管Gli2A是该区域Shh的主要效应器,但下丘脑的特化也依赖于PCP以及神经上皮分泌的Shh对Gli3R的抑制。丘脑是由起源于ZLI的Shh形态发生素梯度按照与脊髓中类似的机制形成模式的。丘脑本身不属于Shh谱系。Gli2A对于丘脑核的适当生长和特化是必需的,但内侧和板内核群(与边缘系统相关)除外,它们的发育依赖于Gli3R。除了特化和模式形成之外,关于这两个区域细胞分选和聚集的现有数据稀少,这也显示了它们之间的关键差异。总之,不仅表达模式,而且发育机制都支持将传统的丘脑和下丘脑分离到不同的前脑节段区域。