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Isolation of Preadipocytes from Broiler Chick Embryos
Published on: August 4, 2022
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Maternal dietary fish oil developmentally programs adipogenic development in the broiler chick embryo
Minjeong Kim1, Usuk Jung1, Jeanna Wilson2
1Department of Animal Science, The University of Tennessee, Knoxville, TN 37996, USA.
Poultry Science
|August 2, 2025
Summary
Maternal fish oil (MFO) in hen diets reduces chick embryo fat accumulation by altering gene expression and DNA methylation. This dietary programming via omega-3 polyunsaturated fatty acids (n-3 PUFA) impacts adipose development, potentially lowering fat post-hatch.
Area of Science:
- Poultry Science
- Developmental Biology
- Nutritional Biochemistry
Background:
- Adipose development in broiler chickens is crucial for meat production.
- Maternal diet composition significantly influences embryonic development and offspring metabolism.
- Omega-3 polyunsaturated fatty acids (n-3 PUFA) are known for their health benefits, but their role in embryonic adipose programming requires further elucidation.
Purpose of the Study:
- To investigate the molecular mechanisms by which fish oil, a source of n-3 PUFA, influences adipose tissue development in chick embryos.
- To determine the effects of maternal fish oil (MFO) versus soybean oil (MSO) on adipocyte morphology, lipid accumulation, and mitochondrial activity in developing chick embryos.
- To analyze the transcriptomic and epigenetic changes induced by MFO in embryonic adipose tissue.
Main Methods:
- Broiler breeder hens were fed diets containing fish oil or soybean oil for four weeks.
- Fertilized eggs were collected and incubated to specific embryonic ages (E14, E16, E20).
- Fatty acid profiling, histological analysis, preadipocyte culture, mitochondrial activity assays, RNA-sequencing (RNA-seq), and DNA methylation analysis were performed.
Main Results:
- Maternal fish oil (MFO) enriched embryonic adipose tissue with EPA and DHA, reduced adipocyte size, and increased the frequency of small adipocytes.
- MFO preadipocytes showed reduced lipid accumulation and enhanced mitochondrial activity compared to MSO controls.
- RNA-seq revealed significant alterations in gene expression in MFO embryos, particularly in lipid metabolism, fatty acid metabolism, and PPAR signaling pathways, including upregulation of Iroquois homeobox genes.
- Differential DNA methylation patterns were observed in response to MFO, with 17 differentially methylated regions identified.
Conclusions:
- Dietary fish oil, rich in n-3 PUFA, programs chick embryos to reduce fat accretion through molecular mechanisms originating during embryonic development.
- Transcriptomic and epigenetic modifications, including changes in lipid metabolism gene expression and DNA methylation, are key mediators of this effect.
- Maternal n-3 PUFA supplementation offers a potential strategy for managing adipose tissue development and potentially reducing fat deposition in broiler chickens post-hatch.

