Cell-fate conversion of intestinal cells in adult Drosophila midgut by depleting a single transcription factor

Xingting Guo, Chenhui Wang (), Yongchao Zhang, Ruxue Wei and Rongwen Xi ()
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Xingting Guo: National Institute of Biological Sciences
Chenhui Wang: National Institute of Biological Sciences
Yongchao Zhang: National Institute of Biological Sciences
Ruxue Wei: National Institute of Biological Sciences
Rongwen Xi: National Institute of Biological Sciences

Nature Communications, 2024, vol. 15, issue 1, 1-16

Abstract: Abstract The manipulation of cell identity by reprograming holds immense potential in regenerative medicine, but is often limited by the inefficient acquisition of fully functional cells. This problem can potentially be resolved by better understanding the reprogramming process using in vivo genetic models, which are currently scarce. Here we report that both enterocytes (ECs) and enteroendocrine cells (EEs) in adult Drosophila midgut show a surprising degree of cell plasticity. Depleting the transcription factor Tramtrack in the differentiated ECs can initiate Prospero-mediated cell transdifferentiation, leading to EE-like cells. On the other hand, depletion of Prospero in the differentiated EEs can lead to the loss of EE-specific transcription programs and the gain of intestinal progenitor cell identity, allowing cell cycle re-entry or differentiation into ECs. We find that intestinal progenitor cells, ECs, and EEs have a similar chromatin accessibility profile, supporting the concept that cell plasticity is enabled by pre-existing chromatin accessibility with switchable transcription programs. Further genetic analysis with this system reveals that the NuRD chromatin remodeling complex, cell lineage confliction, and age act as barriers to EC-to-EE transdifferentiation. The establishment of this genetically tractable in vivo model should facilitate mechanistic investigation of cell plasticity at the molecular and genetic level.

Date: 2024
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DOI: 10.1038/s41467-024-46956-8

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