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Cholangiocytes contribute to hepatocyte regeneration after partial liver injury during growth spurt in zebrafish
by
Libert, Frédérick
, Eski, Sema Elif
, Hovhannisyan, Gabriel Garnik
, Singh, Sumeet Pal
, Mi, Jiarui
, Lefort, Anne
, Pozo-Morales, Macarena
, Barbhaya, Dev
, Manco, Rita
, Andersson, Olov
, Gurzov, Esteban N.
, Marini, Federico
, Perazzolo, Camille
, Ez-Zammoury, Imane
in
14/63
/ 38/39
/ 631/136/2128
/ 631/136/532/489
/ 631/532/489
/ 64/116
/ Ablation
/ Animals
/ Bile Ducts - cytology
/ Cell Transdifferentiation
/ Danio rerio
/ Epithelial Cells - cytology
/ Epithelial Cells - metabolism
/ Hepatectomy
/ Hepatocytes
/ Hepatocytes - cytology
/ Hepatocytes - metabolism
/ Hepatocytes - physiology
/ Humanities and Social Sciences
/ Injuries
/ Liver
/ Liver - cytology
/ Liver - injuries
/ Liver - metabolism
/ Liver Regeneration - physiology
/ Mechanistic Target of Rapamycin Complex 1 - metabolism
/ multidisciplinary
/ Regeneration
/ Science
/ Science (multidisciplinary)
/ Signal Transduction
/ Single-Cell Analysis
/ Transcriptomics
/ Zebrafish
/ Zebrafish - growth & development
/ Zebrafish Proteins - genetics
/ Zebrafish Proteins - metabolism
2025
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Cholangiocytes contribute to hepatocyte regeneration after partial liver injury during growth spurt in zebrafish
by
Libert, Frédérick
, Eski, Sema Elif
, Hovhannisyan, Gabriel Garnik
, Singh, Sumeet Pal
, Mi, Jiarui
, Lefort, Anne
, Pozo-Morales, Macarena
, Barbhaya, Dev
, Manco, Rita
, Andersson, Olov
, Gurzov, Esteban N.
, Marini, Federico
, Perazzolo, Camille
, Ez-Zammoury, Imane
in
14/63
/ 38/39
/ 631/136/2128
/ 631/136/532/489
/ 631/532/489
/ 64/116
/ Ablation
/ Animals
/ Bile Ducts - cytology
/ Cell Transdifferentiation
/ Danio rerio
/ Epithelial Cells - cytology
/ Epithelial Cells - metabolism
/ Hepatectomy
/ Hepatocytes
/ Hepatocytes - cytology
/ Hepatocytes - metabolism
/ Hepatocytes - physiology
/ Humanities and Social Sciences
/ Injuries
/ Liver
/ Liver - cytology
/ Liver - injuries
/ Liver - metabolism
/ Liver Regeneration - physiology
/ Mechanistic Target of Rapamycin Complex 1 - metabolism
/ multidisciplinary
/ Regeneration
/ Science
/ Science (multidisciplinary)
/ Signal Transduction
/ Single-Cell Analysis
/ Transcriptomics
/ Zebrafish
/ Zebrafish - growth & development
/ Zebrafish Proteins - genetics
/ Zebrafish Proteins - metabolism
2025
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Cholangiocytes contribute to hepatocyte regeneration after partial liver injury during growth spurt in zebrafish
by
Libert, Frédérick
, Eski, Sema Elif
, Hovhannisyan, Gabriel Garnik
, Singh, Sumeet Pal
, Mi, Jiarui
, Lefort, Anne
, Pozo-Morales, Macarena
, Barbhaya, Dev
, Manco, Rita
, Andersson, Olov
, Gurzov, Esteban N.
, Marini, Federico
, Perazzolo, Camille
, Ez-Zammoury, Imane
in
14/63
/ 38/39
/ 631/136/2128
/ 631/136/532/489
/ 631/532/489
/ 64/116
/ Ablation
/ Animals
/ Bile Ducts - cytology
/ Cell Transdifferentiation
/ Danio rerio
/ Epithelial Cells - cytology
/ Epithelial Cells - metabolism
/ Hepatectomy
/ Hepatocytes
/ Hepatocytes - cytology
/ Hepatocytes - metabolism
/ Hepatocytes - physiology
/ Humanities and Social Sciences
/ Injuries
/ Liver
/ Liver - cytology
/ Liver - injuries
/ Liver - metabolism
/ Liver Regeneration - physiology
/ Mechanistic Target of Rapamycin Complex 1 - metabolism
/ multidisciplinary
/ Regeneration
/ Science
/ Science (multidisciplinary)
/ Signal Transduction
/ Single-Cell Analysis
/ Transcriptomics
/ Zebrafish
/ Zebrafish - growth & development
/ Zebrafish Proteins - genetics
/ Zebrafish Proteins - metabolism
2025
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Cholangiocytes contribute to hepatocyte regeneration after partial liver injury during growth spurt in zebrafish
Journal Article
Cholangiocytes contribute to hepatocyte regeneration after partial liver injury during growth spurt in zebrafish
2025
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Overview
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 hepatocytes. We further identify active mTORC1 signalling in the uninjured liver of growing animal to be a regulator of the enhanced plasticity of cholangiocytes. Our study suggests cholangiocyte-to-hepatocyte transdifferentiation as the primary mechanism of liver regeneration during periods of rapid growth.
During partial liver injury in growing zebrafish, cholangiocytes regenerate hepatocytes through transdifferentiation, revealing a stage-specific regeneration mechanism regulated by mTORC1 signaling.
Publisher
Nature Publishing Group UK,Nature Publishing Group,Nature Portfolio
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