Evidence map›Paper›PMID 41250076›Full record

ArticleBMC veterinary research2025

Hepatocyte production across embryonic stages in chicken: an in vitro approach.

Maryam Farzaneh, Shirin Azizidoost

Abstract read
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Article in BMC veterinary research, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

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2 · The registry

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

2 authors.

Maryam FarzanehFertility, Infertility and Perinatology Research Center, Ahvaz Jundishapur University of Medical Sciences, Ahvaz, Iran.
Shirin AzizidoostCellular and Molecular Research Center, Medical Basic Sciences Research Institute, Ahvaz Jundishapur University of Medical Sciences, Ahvaz, Iran. shirin_azizidoost@yahoo.com.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundChicken hepatocytes are a valuable resource for cell-based assays and investigating the underlying mechanisms of diseases.

objectiveIn this study, we examined in vitro generation of chicken hepatocytes from three embryonic developmental stages.

methodsHepatocytes were isolated from 5-, 7-, and 10-day-old chicken embryos and cultured in DMEM/F12 + 10% FBS. After 3 days, we measured proliferation rate, the expression of hepatocyte-specific genes (AFP, ALP, FOXA2, CYP3A4, CXCR4, OCT4, NANOG, SOX17), enzyme activity (ALT, AST), albumin production, and urea secretion.

findingsMorphological examination of individual hepatocytes exhibited a characteristic hexagonal structure with prominent nuclei and nucleoli. E10 embryos exhibiting a markedly higher proliferation rate in comparison to those from E5 and E7 stages (until 20 days). Whereas, approximately 50% of E5 and E7 hepatocytes showed reduced proliferation after three days. In suspension culture, hepatocytes formed spheroids or hepatospheres. The expression of hepatocyte-specific genes (AFP, ALP, FOXA2, and CYP3A4) was higher in E10 compared to E5 hepatocytes. The expression of stemness/early developmental markers (CXCR4, OCT4, NANOG, and SOX17) was significantly lower in E10 than E5 hepatocytes. E10 hepatocytes revealed significantly increased ALT and AST expression and urea secretion. While, Albumin production was significantly lower in E10 hepatocytes.

conclusionOur results invested that E10 is the optimal developmental stage for the derivation and proliferation of chicken hepatocytes in vitro.

Indexed as

HepatocytesAnimalsCell Culture TechniquesCell ProliferationChick EmbryoChickensChicken embryoHepatocytesProliferation

Identifiers

PMID41250076
PMCPMC12625007

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