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Method Article

Isolation of Preadipocytes from Broiler Chick Embryos

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DOI:

10.3791/63861

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August 4th, 2022

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In This Article

Summary

The present protocol describes a simple method for isolating preadipocytes from adipose tissue in broiler embryos. This method enables isolation with high yield, primary culture, and adipogenic differentiation of preadipocytes. Oil Red O staining and lipid/DNA stain measured the adipogenic ability of isolated cells induced with differentiation media.

Abstract

Primary preadipocytes are a valuable experimental system for understanding the molecular pathways that control adipocyte differentiation and metabolism. Chicken embryos provide the opportunity to isolate preadipocytes from the earliest stage of adipose development. This primary cell can be used to identify factors influencing preadipocyte proliferation and adipogenic differentiation, making them a valuable model for studies related to childhood obesity and control of excess fat deposition in poultry. The rapid growth of postnatal adipose tissue effectively wastes feed by allocating it away from muscle growth in broiler chickens. Therefore, methods to understand the earliest stages of adipose tissue development may provide clues to regulate this tendency and identify ways to limit adipose expansion early in life. The present study was designed to develop an efficient method for isolation, primary culture, and adipogenic differentiation of preadipocytes isolated from developing adipose tissue of commercial broiler (meat-type) chick embryos. The procedure has been optimized to yield cells with high viability (~98%) and increased capacity to differentiate into mature adipocytes. This simple method of embryonic preadipocyte isolation, culture, and differentiation supports functional analyses of fat growth and development in early life.

Introduction

Obesity is a global health threat to both adults and children. Children who are overweight or obese are approximately five times more likely to be obese as adults, placing them at significantly increased risk for cardiovascular disease, diabetes, and many other comorbidities. About 13.4% of US children aged 2-5 have obesity1, illustrating that the tendency to accumulate excess body fat can be set in motion very early in life. For very different reasons, the accumulation of excess adipose tissue is a concern for broiler (meat-type) chickens. Modern broilers are incredibly efficient but still accumulate more lipid than is physiologically necessar....

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Protocol

All animal procedures were approved by the University of Tennessee Institutional Animal Care and Use Committee. Freshly fertilized commercial broiler eggs (Cobb 500) were obtained from a local hatchery. Eggs were incubated at 38 °C with 60% relative humidity until dissections at embryonic days 16-18 (E16-E18). Adipose tissue was collected from the subcutaneous (femoral) depot.

1. Preparation for isolation and culture

  1. Prepare the culture hood and the instruments.
    1. Before starting dissections, set up a work area in the laminar-flow hood. Disinfect the working area and all the instruments by swabbin....

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Results

Primary preadipocytes are morphologically similar to fibroblasts, with irregular, star-like shapes and a central nucleus (Figure 2A-C). The cells readily adhere to tissue culture plastic and begin to proliferate soon after attachment. They rapidly differentiate and accumulate lipid droplets (Figure 3D) when provided with fatty acids in the media. The viability (98%, based on dye exclusion) reported in the isolations represented .......

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Discussion

Although several well-described protocols have reported the isolation of preadipocytes14,15,16,17, isolation for embryonic preadipocytes has been optimized, which can be used for functional analyses of early life fat growth and development in broiler chicks. This protocol yields high viability embryonic adipocyte progenitors with high differentiation potential. Moreover, the presented procedure.......

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Disclosures

The authors have nothing to disclose.

Acknowledgements

The authors thank UT AgResearch and the Department of Animal Science for supporting and optimizing this protocol. This work was funded by USDA grant.

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Materials

List of materials used in this article
NameCompanyCatalog NumberComments
1 mL PipetteEppendorfZ683825Single Channel Pipette, 100 - 1000 µL
1 mL Pipette TipFisher Scientific02-707-402
100% IsopropanolFisher ScientificA426P4
1x PBSGibco10010023
25 mL FlaskPyrex4980-25
37% FormaldehydeFisher ScientificF75P-1GAL
6-Well PlateFalcon353046Tissue Culture-treated
96-Well Assay PlateCostar3632
96-Well Plate, Black BottomCostar3603Tissue Culture-treated
AdipoRedLonzaPT-7009
Amphotericin BGibco15290026
Bench Top Wiper (Kimtechwiper)Kimberly-Clark34155
BetadineUp & UpNDC 116730033420% Working Solution
Cell CounterCorning6749
Cell Strainer, 40 µmSPL93040
CentrifugatonEppendorf5702
Chicken SerumGibco16110082
Conical Centrifuge Tubes, 15 mLVWR10025-690
Conical Centrifuge Tubes, 50 mLFalcon352098
CryovialNunc343958
Curved Forceps, 100 mmRoboz SurgicalRS-5137
Curved Surgical Scissors, 115 mmRoboz SurgicalRS-6839
Distilled WaterMilliporeSYNSV0000Despensed as needed
DMEM/F12HyCloneSH30023.01
DMSOSigmaD2650
EthanolDecon Labs270170% Working Solution
Fetal Bovine Serum (FBS)Gibco10437028
Fluorescent MicroscopeEVOSM7000
Fluorescent Plate ReaderBiotekSynergy H1
FoilReynoldsReynolds Wrap Heavy Duty Aluminum Foil, 125 SQ. FT.
Freezing ContainerThermo Scientific5100-0001
GelatinMillipore40552% Working Solution
Hematocytometer (Counting Chamber)Corning4802000.1 mm deep
IncubatorFisher Scientific6845
Instrument SterilizerVWRB1205
Linoleic Acid-Oleic Acid-AlbuminSigmaL96551x Working Solution
MicroscopeEvosAMEX1000
Multi-Channel PipetteThermo Scientific466107012-Channel Pipetters, 30 - 300 µL
Na2HPO4SigmaS-7907
NaH2PO4SigmaS-3139
NucBlueInvitrogenR37605
Oil Red OSigmaO-0625
Orbital ShakerIKAKS130BS1
Paper TowelTorkRK8002
ParafilmParafilm MPM996
Penicillin/Steptomycin (P/S)Gibco151401221x Working Solution
Petri dishes, 100 mmFalcon351029
Petri dishes, 60 mmFalcon351007
Plate ShakerVWR200
RBC Lysis BufferRoche11814389001
Reagent ReserviorVWR89094-680
Small Beaker, 100 mLPyrex1000-100
Spectrophotometer Plate ReaderBiotekSynergy H1
Sterile GauzeMcKesson762703
Straight Forceps, 120 mmRoboz SurgicalRS-4960
Straight Scissors, 140 mmRoboz SurgicalRS-6762
T-25 FlaskCorning430639Tissue Culture-treated
Tissue Culture IncubatorThermo Scientific50144906
Tissue Strainer, 250 µmPierce87791
Trypan Blue StainGibco15250061
TrypsinGibco154000540.1% Working Solution
Tweezers, 110 mmRoboz SurgicalRS-5035
Type 1 CollagenaseGibco17100017
Water BathFisher Scientific15-462-10
Whatman Grade 1 Filter PaperWhatman1001-110

References

  1. Fryar, C. D., Carroll, M. D., Ogden, C. L. Prevalence of overweight, obesity, and severe obesity among children and adolescents aged 2-19 years: United States, 1963-1965 through 2015-2016. , (2018).
  2. Siegel, P. B. Evolutio....

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