{"doi":"10.1101/2020.06.01.127712","title":"De novo enteric neurogenesis in post-embryonic zebrafish from Schwann cell precursors rather than resident cell types","abstract":"ABSTRACT The enteric nervous system is essential for normal gastrointestinal function, but evidence regarding postnatal enteric neurogenesis is conflicting. Using zebrafish as a model, we explored the origin of enteric neurons that arise in post-embryonic life in normal development and injury, and tested effects of the 5-HT 4 receptor agonist, prucalopride. To assess enteric neurogenesis, all enteric neurons were photoconverted prior to time-lapse imaging to detect emergence of new neurons. Injury was modeled by two-photon laser ablation of enteric neurons. Lineage tracing was performed with neural tube injections of lipophilic dye and with an inducible Sox10-Cre line. Lastly, we tested prucalopride’s effect on post-embryonic enteric neurogenesis. The post-embryonic zebrafish intestine appears to lack resident neurogenic precursors and enteric glia. However, enteric neurogenesis persists post-embryonically during development and after injury. New enteric neurons arise from trunk neural crest-derived Schwann cell precursors. Prucalopride increases enteric neurogenesis in normal development and after injury if exposure occurs prior to injury. Enteric neurogenesis persists in the post-embryonic period in both normal development and injury, appears to arise from gut-extrinsic Schwann cell precursors, and is promoted by prucalopride. SUMMARY STATEMENT Trunk crest-derived enteric neurogenesis is poorly understood. We find post-embryonic zebrafish lack resident neuronal precursors yet enteric neurogenesis from trunk crest-derived precursors occurs in development, injury, and is promoted by prucalopride.","journal":"bioRxiv (Cold Spring Harbor Laboratory)","year":2020,"id":120012,"datarank":0.0,"base_score":0.0,"endowment":0.0,"self_citation_contribution":0.0,"citation_network_contribution":0.0,"self_endowment_contribution":0.0,"citer_contribution":0.0,"corpus_percentile":null,"corpus_rank":null,"citation_count":13,"citer_count":0,"citers_with_citation_signal":0,"citers_with_endowment":0,"datacite_reuse_total":0,"is_dataset":false,"is_dataset_confidence":0.9563,"is_data_producer":false,"deposit_databanks":null,"is_oa":true,"file_count":0,"downloads":0,"has_version_chain":false,"published_date":"2020-01-01","fair_score":null,"fair_percentile":null,"algorithm_id":"datarank_citation_only_1hop_v6","ranking_scope":"data_only","authors":[{"id":294393,"name":"Marianne Bronner‐Fraser","orcid":"0000-0003-4274-1862","position":1,"is_corresponding":false},{"id":27733,"name":"Wael N. El‐Nachef","orcid":"0000-0002-2892-9394","position":0,"is_corresponding":true}],"reference_count":60,"raw_metadata":null,"created_at":"2026-07-18T23:14:13.002105Z","pmid":null,"pmcid":null,"fwci":null,"citation_percentile":null,"influential_citations":0,"oa_status":null,"license":null,"views":0,"total_file_size_bytes":0,"version_count":0,"fair_f":null,"fair_a":null,"fair_i":null,"fair_r":null,"fair_zscore":null,"fair_rationale":null,"fair_model":null,"fair_agent_version":null,"fair_fulltext_source":null,"fair_has_llm":null,"fair_computed_at":null,"clinical_trials":[],"software_tools":[],"db_accessions":[],"linked_datasets":[],"topics":[]}