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Construction of a human cell landscape at single-cell level.

Xiaoping HanZiming ZhouLijiang FeiHuiyu SunRenying WangYao ChenHaide ChenJingjing WangHuanna TangWenhao GeYincong ZhouFang YeMengmeng JiangJunqing WuYanyu XiaoXiaoning JiaTingyue ZhangXiaojie MaQi ZhangXueli BaiShujing LaiChengxuan YuLijun ZhuRui LinYuchi GaoMin WangYiqing WuJianming ZhangRenya ZhanSaiyong ZhuHai-Lan HuChangchun WangMing ChenHe HuangTingbo LiangJianghua ChenWeilin WangDan ZhangGuoji Guo
Published in: Nature (2020)
Single-cell analysis is a valuable tool for dissecting cellular heterogeneity in complex systems1. However, a comprehensive single-cell atlas has not been achieved for humans. Here we use single-cell mRNA sequencing to determine the cell-type composition of all major human organs and construct a scheme for the human cell landscape (HCL). We have uncovered a single-cell hierarchy for many tissues that have not been well characterized. We established a 'single-cell HCL analysis' pipeline that helps to define human cell identity. Finally, we performed a single-cell comparative analysis of landscapes from human and mouse to identify conserved genetic networks. We found that stem and progenitor cells exhibit strong transcriptomic stochasticity, whereas differentiated cells are more distinct. Our results provide a useful resource for the study of human biology.
Keyphrases
  • single cell
  • rna seq
  • endothelial cells
  • high throughput
  • induced pluripotent stem cells
  • cell death
  • induced apoptosis
  • gene expression
  • mesenchymal stem cells
  • transcription factor
  • endoplasmic reticulum stress