Institute of Medical Biology Chinese Academy of Medical Sciences, Chinese Academy of Medical Science and Peking Union Medical College, Kunming, China.
Department of Molecular Biology and Biochemistry, Institute of Basic Medical Sciences, Medical Primate Research Center, Neuroscience Center, Chinese Academy of Medical Sciences, School of Basic Medicine Peking Union Medical College, Beijing, China.
Elife. 2024 Feb 28;12:RP90325. doi: 10.7554/eLife.90325.
Despite intense research on mice, the transcriptional regulation of neocortical neurogenesis remains limited in humans and non-human primates. Cortical development in rhesus macaque is known to recapitulate multiple facets of cortical development in humans, including the complex composition of neural stem cells and the thicker supragranular layer. To characterize temporal shifts in transcriptomic programming responsible for differentiation from stem cells to neurons, we sampled parietal lobes of rhesus macaque at E40, E50, E70, E80, and E90, spanning the full period of prenatal neurogenesis. Single-cell RNA sequencing produced a transcriptomic atlas of developing parietal lobe in rhesus macaque neocortex. Identification of distinct cell types and neural stem cells emerging in different developmental stages revealed a terminally bifurcating trajectory from stem cells to neurons. Notably, deep-layer neurons appear in the early stages of neurogenesis, while upper-layer neurons appear later. While these different lineages show overlap in their differentiation program, cell fates are determined post-mitotically. Trajectories analysis from ventricular radial glia (vRGs) to outer radial glia (oRGs) revealed dynamic gene expression profiles and identified differential activation of , , and signaling pathways between vRGs and oRGs. These results provide a comprehensive overview of the temporal patterns of gene expression leading to different fates of radial glial progenitors during neocortex layer formation.
尽管对小鼠进行了深入研究,但神经发生的转录调控在人类和非人类灵长类动物中仍然有限。众所周知,猕猴的皮质发育可以重现人类皮质发育的多个方面,包括神经干细胞的复杂组成和较厚的颗粒上层。为了描述负责从干细胞分化为神经元的转录组编程的时间变化,我们在 E40、E50、E70、E80 和 E90 时采样了猕猴的顶叶,跨越了整个产前神经发生时期。单细胞 RNA 测序产生了猕猴新皮质顶叶发育的转录组图谱。鉴定出在不同发育阶段出现的不同细胞类型和神经干细胞,揭示了从干细胞到神经元的终末分叉轨迹。值得注意的是,深层神经元出现在神经发生的早期,而上层神经元出现较晚。虽然这些不同的谱系在其分化程序中存在重叠,但细胞命运是在有丝分裂后确定的。从室管膜径向胶质(vRGs)到外放射状胶质(oRGs)的轨迹分析揭示了动态的基因表达谱,并确定了 vRGs 和 oRGs 之间 、 和 信号通路的差异激活。这些结果提供了一个全面的概述,说明了导致新皮质层形成过程中放射状胶质祖细胞不同命运的基因表达的时间模式。