Fame Ryann M, MacDonald Jessica L, Dunwoodie Sally L, Takahashi Emi, Macklis Jeffrey D
Department of Stem Cell and Regenerative Biology, Center for Brain Science, and Harvard Stem Cell Institute, Harvard University, Cambridge, Massachusetts 02138.
Developmental and Stem Cell Biology Division, Victor Chang Cardiac Research Institute, Darlinghurst, Sydney, New South Wales, 2052 Australia, Faculties of Medicine and Science, University of New South Wales, Kensington, Sydney, New South Wales, 2052 Australia.
J Neurosci. 2016 Jun 15;36(24):6403-19. doi: 10.1523/JNEUROSCI.4067-15.2016.
The neocortex contains hundreds to thousands of distinct subtypes of precisely connected neurons, allowing it to perform remarkably complex tasks of high-level cognition. Callosal projection neurons (CPN) connect the cerebral hemispheres via the corpus callosum, integrating cortical information and playing key roles in associative cognition. CPN are a strikingly diverse set of neuronal subpopulations, and development of this diversity requires precise control by a complex, interactive set of molecular effectors. We have found that the transcriptional coregulator Cited2 regulates and refines two stages of CPN development. Cited2 is expressed broadly by progenitors in the embryonic day 15.5 subventricular zone, during the peak of superficial layer CPN birth, with a progressive postmitotic refinement in expression, becoming restricted to CPN of the somatosensory cortex postnatally. We generated progenitor-stage and postmitotic forebrain-specific Cited2 conditional knock-out mice, using the Emx1-Cre and NEX-Cre mouse lines, respectively. We demonstrate that Cited2 functions in progenitors, but is not necessary postmitotically, to regulate both (1) broad generation of layer II/III CPN and (2) acquisition of precise area-specific molecular identity and axonal/dendritic connectivity of somatosensory CPN. This novel CPN subtype-specific and area-specific control from progenitor action of Cited2 adds yet another layer of complexity to the multistage developmental regulation of neocortical development.
This study identifies Cited2 as a novel subtype-specific and area-specific control over development of distinct subpopulations within the broad population of callosal projection neurons (CPN), whose axons connect the two cerebral hemispheres via the corpus callosum (CC). Currently, how the remarkable diversity of CPN subtypes is specified, and how they differentiate to form highly precise and specific circuits, are largely unknown. We found that Cited2 functions within subventricular zone progenitors to both broadly regulate generation of superficial layer CPN throughout the neocortex, and to refine precise area-specific development and connectivity of somatosensory CPN. Gaining insight into molecular development and heterogeneity of CPN will advance understanding of both diverse functions of CPN and of the remarkable range of neurodevelopmental deficits correlated with CPN/CC development.
新皮质包含数百到数千种精确连接的神经元亚型,使其能够执行极其复杂的高级认知任务。胼胝体投射神经元(CPN)通过胼胝体连接大脑半球,整合皮质信息并在联想认知中发挥关键作用。CPN是一组极为多样的神经元亚群,这种多样性的发育需要一组复杂的、相互作用的分子效应器进行精确控制。我们发现转录共调节因子Cited2调节和完善CPN发育的两个阶段。Cited2在胚胎第15.5天的脑室下区广泛由祖细胞表达,此时正是浅层CPN产生的高峰期,其表达在有丝分裂后逐渐细化,出生后局限于体感皮质的CPN。我们分别使用Emx1-Cre和NEX-Cre小鼠品系,生成了祖细胞阶段和有丝分裂后前脑特异性Cited2条件性敲除小鼠。我们证明Cited2在祖细胞中发挥作用,但在有丝分裂后并非必需,以调节:(1)广泛产生II/III层CPN;(2)获得体感CPN精确的区域特异性分子特性以及轴突/树突连接性。Cited2从祖细胞作用对CPN进行的这种新的亚型特异性和区域特异性控制,为新皮质发育的多阶段发育调节增添了另一层复杂性。
本研究确定Cited2是对胼胝体投射神经元(CPN)广泛群体中不同亚群发育的一种新的亚型特异性和区域特异性控制,其轴突通过胼胝体(CC)连接两个大脑半球。目前,CPN亚型的显著多样性是如何确定的,以及它们如何分化形成高度精确和特异的回路,在很大程度上尚不清楚。我们发现Cited2在脑室下区祖细胞内发挥作用,既广泛调节整个新皮质浅层CPN的产生,又完善体感CPN精确的区域特异性发育和连接性。深入了解CPN的分子发育和异质性将促进对CPN的多种功能以及与CPN/CC发育相关的广泛神经发育缺陷的理解。