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Cholangiocytes contribute to hepatocyte regeneration after partial liver injury during growth spurt in zebrafish

Nature Communication. 2025-06; 
Sema Elif Eski, Jiarui Mi, Macarena Pozo-Morales, Gabriel Garnik Hovhannisyan, Camille Perazzolo, Rita Manco, Imane Ez-Zammoury, Dev Barbhaya, Anne Lefort, Frédérick Libert, Federico Marini, Esteban N Gurzov, Olov Andersson, Sumeet Pal Singh
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Gene Synthesis To generate the fabp10a:lox2272-loxp-nls-mTagBFP2-stop-lox2272- H2B-mGL-stop-loxp-mCherry-NTR; cryaa:mCherry construct [abbreviated as fabp10a:BB-NTR], the dsDNA sequence of BB-NTR flanked with EcoRI/PacI was synthesized by GenScript Biotech and used to replace flag-SpiCee-mRFP1 in the fabp10a:flag-SpiCeemRFP1;cryaa:mCherry construct61 using restriction enzyme-based cloning with EcoRI/PacI following by ligation with T4 ligase. Get A Quote

摘要

The liver's regenerative ability depends on injury extent. Minor injuries are repaired by hepatocyte self-duplication, while severe damage triggers cholangiocyte involvement in hepatocyte recovery. This paradigm is well-documented for adult animals but is less explored during rapid growth. We design two partial liver injury models in zebrafish, which were investigated during growth spurts: 1) partial ablation, killing half the hepatocytes; and 2) partial hepatectomy, removing half a liver lobe. In both injuries, de novo hepatocytes emerged alongside existing ones. Single-cell transcriptomics and lineage tracing with Cre-driver lines generated by genome editing identified cholangiocytes as the source of de novo ... More

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