Identification of TOR-responsive slow-cycling neoblasts in planarians

• Published in: EMBO reports Vol. 22; no. 3; pp. e50292 - n/a
• Main Authors: Molinaro, Alyssa M, Lindsay-Mosher, Nicole, Pearson, Bret J
• Format: Journal Article
• Language: English
• Published: London Nature Publishing Group UK 03.03.2021; Blackwell Publishing Ltd; John Wiley and Sons Inc
• Subjects: Amputation; Animals; Cell activation; Cell cycle; Cycles; EMBO34; Fluorescence; Heterogeneity; Homeostasis; planarians; Planarians - genetics; quiescence; Regeneration; Regenerators; Stem Cells; TORC1; Transcription; Tumor suppressor genes; Tumors; Turbellaria; stem cells; TORC1; quiescence; planarians; regeneration
• ISSN: 1469-221X; 1469-3178
• DOI: 10.15252/embr.202050292

Epimorphic regeneration commonly relies on the activation of reserved stem cells to drive new cell production. The planarian Schmidtea mediterranea is among the best regenerators in nature, thanks to its large population of adult stem cells, called neoblasts. While neoblasts have long been known to drive regeneration, whether a subset of neoblasts is reserved for this purpose is unknown. Here, we revisit the idea of reserved neoblasts by approaching neoblast heterogeneity from a regulatory perspective. By implementing a new fluorescence-activated cell sorting strategy in planarians, we identify a population of neoblasts defined by low transcriptional activity. These RNA low neoblasts are relatively slow-cycling at homeostasis and undergo a morphological regeneration response characterized by cell growth at 48 h post-amputation. At this time, RNA low neoblasts proliferate in a TOR-dependent manner. Additionally, knockdown of the tumour suppressor Lrig-1 , which is enriched in RNA low neoblasts, results in RNA low neoblast growth and hyperproliferation at homeostasis, and ultimately delays regeneration. We propose that slow-cycling RNA low neoblasts represent a regeneration-reserved neoblast population. SYNOPSIS Slow-cycling RNA low neoblasts grow and enter the cell cycle following amputation in a TOR-dependent manner. These findings suggest that planarians use a slow-cycling adult stem cell strategy in their regenerative biology. Planarians have relatively long-term label-retaining neoblasts. RNA low neoblasts have low transcriptional and proliferative activity at homeostasis. RNA low neoblasts undergo TOR-dependent growth and cell cycle entry during regeneration. Graphical Abstract A population of slow-cycling RNA low neoblasts in the planarian Schmidtea mediterranea grows and enters the cell cycle following amputation in a TOR-dependent manner. These findings suggest that planarians use a slow-cycling adult stem cell strategy in their regenerative biology.