bioRxivDevelopmental BiologyPreprint
Single cell transcriptome analysis reveals markers of naive and lineage-primed hematopoietic progenitors derived from human pluripotent stem cells.
Antonella FidanzaiD, Nicola RomanòiD, Prakash RamachandraniD, Sara TamagnoiD, Martha Lopez‐YrigoyeniD, Alice Helen Taylor, Jennifer E. Easterbrook, Beth E. P. HendersoniD, Richard A Axton, Neil Cowan HendersoniD, Alexander MedvinskyiD, Katrin OttersbachiD, Lesley M. ForresteriD
Abstract
During embryogenesis the hematopoietic system develops through distinct waves that generate progenitors with increasing lineage potential, ultimately producing haematopoietic stem cells (HSCs). In vitro differentiation of human pluripotent stem cells (hPSCs) follows the early steps of haematopoietic development but the production of HSCs has proven more challenging. To study the dynamics and heterogeneity of hematopoietic progenitor cells generated in vitro from hPSCs, we performed RNA sequencing of over 10000 CD235a-CD43+single cells. We identified the transcriptome of naive progenitors and those primed toward erythroid, megakaryocyte and leukocyte lineages, and revealed their markers by clustering, trajectory analyses and functional assays. CD44 marks naive clonogenic progenitors that express the transcription factor, LMO4 and can be expanded upon BMP4 stimulation. Naive progenitors give rise to primed CD326+erythroid, ICAM2+CD9+megakaryocyte, and monocyte, neutrophil and eosinophil progenitors. We have generated an online dataset of human hematopoietic progenitors and their transcriptional remodelling upon lineage priming.
- organism: human
- assay: scRNA-seq
- research focus: cell type annotation
- research focus: clustering
- research focus: trajectory inference
- approach: statistical model
- Citations
- 2
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