Single-cell transcriptome analysis reveals cell lineage specification in temporal-spatial patterns in human cortical development.
Xiaoying FanXin ZhouLe SunMing YangMengdi WangRuiguo ChenQian WuJun YongJi DongLu WenJie QiaoXiaoqun WangFu-Chou TangPublished in: Science advances (2020)
Neurogenesis processes differ in different areas of the cortex in many species, including humans. Here, we performed single-cell transcriptome profiling of the four cortical lobes and pons during human embryonic and fetal development. We identified distinct subtypes of neural progenitor cells (NPCs) and their molecular signatures, including a group of previously unidentified transient NPCs. We specified the neurogenesis path and molecular regulations of the human deep-layer, upper-layer, and mature neurons. Neurons showed clear spatial and temporal distinctions, while glial cells of different origins showed development patterns similar to those of mice, and we captured the developmental trajectory of oligodendrocyte lineage cells until the human mid-fetal stage. Additionally, we verified region-specific characteristics of neurons in the cortex, including their distinct electrophysiological features. With systematic single-cell analysis, we decoded human neuronal development in temporal and spatial dimensions from GW7 to GW28, offering deeper insights into the molecular regulations underlying human neurogenesis and cortical development.
Keyphrases
- single cell
- endothelial cells
- rna seq
- induced pluripotent stem cells
- spinal cord
- stem cells
- high throughput
- type diabetes
- induced apoptosis
- cerebral ischemia
- cell therapy
- genome wide
- cell proliferation
- dna methylation
- blood brain barrier
- cell death
- skeletal muscle
- spinal cord injury
- single molecule
- adipose tissue
- mesenchymal stem cells
- insulin resistance
- endoplasmic reticulum stress