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Abstract
Adult pluripotent stem cell (aPSC) populations underlie whole-body regeneration in many distantly-related animal lineages, but how the underlying cellular and molecular mechanisms compare across species is unknown. Here, we apply single-cell RNA sequencing to profile transcriptional cell states of the acoel worm Hofstenia miamia during postembryonic development and regeneration. We identify cell types shared across stages and their associated gene expression dynamics during regeneration. Functional studies confirm that the aPSCs, also known as neoblasts, are the source of differentiated cells and reveal transcription factors needed for differentiation. Subclustering of neoblasts recovers transcriptionally distinct subpopulations, the majority of which are likely specialized to differentiated lineages. One neoblast subset, showing enriched expression of the histone variant H3.3, appears to lack specialization. Altogether, the cell states identified in this study facilitate comparisons to other species and enable future studies of stem cell fate potentials.
Multiple species can achieve whole-body regeneration through the action of adult stem cells, though little is known about how these cells compare across species. Here they investigated the stem cells of a marine worm, the acoel Hofstenia miamia, and identified heterogeneity of these cells during development and regeneration.
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1 Harvard University, Department of Organismic and Evolutionary Biology, Museum of Comparative Zoology, Cambridge, USA (GRID:grid.38142.3c) (ISNI:000000041936754X)
2 Harvard University, Department of Organismic and Evolutionary Biology, Museum of Comparative Zoology, Cambridge, USA (GRID:grid.38142.3c) (ISNI:000000041936754X); Academia Sinica, Biodiversity Research Center, Taipei, Taiwan (GRID:grid.28665.3f) (ISNI:0000 0001 2287 1366)
3 Harvard University, Department of Organismic and Evolutionary Biology, Museum of Comparative Zoology, Cambridge, USA (GRID:grid.38142.3c) (ISNI:000000041936754X); Harvard University, Department of Molecular and Cell Biology, Cambridge, USA (GRID:grid.38142.3c) (ISNI:000000041936754X)