Transcriptomic Characterization of Key Factors and Signaling Pathways for the Regeneration of Partially Hepatectomized Liver in Zebrafish.

Int J Mol Sci

Key Laboratory of Breeding Biotechnology and Sustainable Aquaculture, Institute of Hydrobiology, Chinese Academy of Sciences, Wuhan 430072, China.

Published: June 2024

AI Article Synopsis

  • This study investigates liver regeneration in zebrafish after partial hepatectomy (PHx), revealing that lost liver mass can regenerate completely within seven days.
  • Researchers used RNA sequencing to identify and classify gene expression profiles during liver regeneration, linking early responsive genes to hormone activity and late responsive genes to detoxification processes.
  • The study highlights the role of the proteasome in liver regeneration, suggesting that inhibiting its activity increases hepatocyte proliferation, providing new insights into liver regeneration mechanisms.

Article Abstract

Liver regeneration induced by partial hepatectomy (PHx) has attracted intensive research interests due to the great significance for liver resection and transplantation. The zebrafish () is an excellent model to study liver regeneration. In the fish subjected to PHx (the tip of the ventral lobe was resected), the lost liver mass could be fully regenerated in seven days. However, the regulatory mechanisms underlying the liver regeneration remain largely unknown. In this study, gene expression profiles during the regeneration of PHx-treated liver were explored by RNA sequencing (RNA-seq). The genes responsive to the injury of PHx treatment were identified and classified into different clusters based on the expression profiles. Representative gene ontology (GO) enrichments for the early responsive genes included hormone activity, ribosome biogenesis and rRNA processing, etc., while the late responsive genes were enriched in biological processes such as glutathione metabolic process, antioxidant activity and cellular detoxification. The Kyoto Encyclopedia of Genes and Genomes (KEGG) pathway enrichments were also identified for the differentially expressed genes (DEGs) between the time-series samples and the sham controls. The proteasome was overrepresented by the up-regulated genes at all of the sampling time points. Inhibiting proteasome activity by the application of MG132 to the fish enhanced the expression of Pcna (proliferating cell nuclear antigen), an indicator of hepatocyte proliferation after PHx. Our data provide novel insights into the molecular mechanisms underlying the regeneration of PHx-treated liver.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC11241411PMC
http://dx.doi.org/10.3390/ijms25137212DOI Listing

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