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Research advances of adipocyte differentiation in poultry

Published online by Cambridge University Press:  14 October 2019

W. WANG*
Affiliation:
Academy of Life Science and Resource Environment of YiChun University, YiChun, 336000, China and Institute of Biological Technology, Jiang Xi Province Key Lab of Genetic Improvement of Indigenous Chicken Breeds, Nanchang Normal University, Nanchang 330032, Jiangxi Province, China
*
Corresponding author: [email protected]
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Abstract

Preadipocytes are distinct precursor cells with the ability to generate and differentiate into adipocytes - a process that is regulated by a variety of genes. Adipocyte differentiation has been extensively studied in mammals; however, little is known about adipocyte differentiation in poultry. This review summarises the isolation, in vitro culture and characterisation of poultry preadipocytes. The most commonly used method for isolating primary preadipocytes is collagenase digestion and the cells are cultured in an incubator with 5% CO2 at 37°C. Preadipocytes of most species can differentiate into mature adipocytes using a combination of growth factors (a so-called ‘hormone cocktail’), which include 3-isobutyl-1-methylxanthine (IBMX), dexamethasone (DEX) and insulin. Only the addition of a fatty acid mixture, transferrin, insulin and albumin induced primary preadipocyte differentiation, indicating that exogenous fatty acids are key factors that influence this process in chickens. As for the molecular regulation of poultry preadipocytes, studies have found several transcription factors that regulate adipose differentiation, which included peroxisome proliferator-activated receptors (PPARs), CCAAT/enhancer binding proteins (C/EBPs) and sterol response element-binding proteins (SREBPs). These transcription factors have been shown to regulate adipocyte differentiation by affecting the expression levels or activity of target genes.

Type
Review
Copyright
Copyright © World's Poultry Science Association 2019 

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References

BAI, S., WANG, G., ZHANG, W., ZHANG, S., RICE, B.B., CLINE, M.A. and GILBERT, E.R. (2015) Broiler chicken adipose tissue dynamics during the first two weeks post-hatch. Comparative Biochemistry and Physiology A-molecular & Integrative Physiology 189: 115-123.Google Scholar
BLACK, P.N., AHOWESSO, C., MONTEFUSCO, D., SAINI, N. and DIRUSSO, C.C. (2016) Fatty Acid Transport Proteins:Targeting FATP2 as a Gatekeeper Involved in the Transport of Exogenous Fatty Acids. MEDCHEMCOMM 7: 612-622.Google Scholar
BOHAN, A.E., PURVIS, K.N., BARTOSH, J.L. and BRANDEBOURG, T.D. (2014) The proliferation and differentiation of primary pig preadipocytes is suppressed when cultures are incubated at 37°Celsius compared to euthermic conditions in pigs. Adipocyte 3: 322-332.Google Scholar
CHEN, Y.C., WU, C.Y. and ZHANG, Z.W. (2017) Effect of Krüppel-like factor 2 (KLF2) over-expression on activities of chicken PPARγ and C/EBPα promoters. Journal of cellular and molecular immunology 8: 1045-1050.Google Scholar
CHENG, B., WU, M., XU, S., ZHANG, X., WANG, Y., WANG, N., LENG, L. and LI, H. (2016) Cocktail supplement with rosiglitazone: a novel inducer for chicken preadipocyte differentiation in vitro. Bioscience Reports 36: e00401.Google Scholar
CRYER, J., WOODHEAD, B.G. and CRYER, A. (1987) The isolation and characterisation of a putative adipocyte precursor cell type from the white adipose tissue of the chicken (Gallus domesticus). Comparative Biochemistry and Physiology A-molecular & Integrative Physiology 86: 515-521.Google Scholar
DING, F., LI, Q.Q., LI, L., GAN, C., YUAN, X., GOU, H., HE, H., HAN, C.C. and WANG, J.W. (2015) Isolation, culture and differentiation of duck (Anas platyrhynchos) preadipocytes. Cytotechnology 67: 773-781.Google Scholar
DING, F., PAN, Z., KOU, J., LI, L., XIA, L., HU, S., LIU, H. and WANG, J. (2012) De novo lipogenesis in the liver and adipose tissues of ducks during early growth stages after hatching. Comparative Biochemistry and Physiology B-biochemistry & Molecular Biology 163: 154-160.Google Scholar
DING, F., QIU, J., LI, Q., HU, J., SONG, C., HAN, C., HE, H. and WANG, J. (2016) Effects of rosiglitazone on proliferation and differentiation of duck preadipocytes. In Vitro Cellular & Developmental Biology-animal 52: 174-181.Google Scholar
DING, N., GAO, Y., WANG, N. and LI, H. (2011) Functional analysis of the chicken PPARgamma gene 5'-flanking region and C/EBPalpha-mediated gene regulation. Comparative Biochemistry and Physiology B-biochemistry & Molecular Biology 158: 297-303.Google Scholar
DUAN, K., SUN, Y., ZHANG, X., ZHANG, T., ZHANG, W., ZHANG, J., WANG, G., WANG, S., LENG, L., LI, H. and WANG, N. (2015) Identification and characterization of transcript variants of chicken peroxisome proliferator-activated receptor gamma. Poultry Science 94: 2516-2527.Google Scholar
FAN, L., HSIEH, P.N., SWEET, D.R. and JAIN, M.K. (2017) Kruppel-like factor 15: Regulator of BCAA metabolism and circadian protein rhythmicity. Pharmacological Research 130: 123-126.Google Scholar
GUO, L., SUN, B., SHANG, Z., LENG, L., WANG, Y., WANG, N. and LI, H. (2011) Comparison of adipose tissue cellularity in chicken lines divergently selected for fatness. Poultry Science 90: 2024-2034.Google Scholar
HASSAN, A., AHN, J., SUH, Y., CHOI, Y.M., CHEN, P. and LEE, K. (2014) Selenium promotes adipogenic determination and differentiation of chicken embryonic fibroblasts with regulation of genes involved in fatty acid uptake, triacylglycerol synthesis and lipolysis. Journal of Nutritional Biochemistry 25: 858-867.Google Scholar
HE, J., TIAN, Y., LI, J.J., SHEN, J.D., TAO, Z.R., FU, Y., NIU, D. and LU, L.Z. (2012) Expression pattern of adipocyte fatty acid-binding protein gene in different tissues and its regulation of genes related to adipocyte differentiation in duck. Poultry Science 91: 2270-2274.Google Scholar
HOCKING, P.M. (2014) Unexpected consequences of genetic selection in broilers and turkeys: problems and solutions. British Poultry Science 55: 1-12.Google Scholar
KLEIN, R.H., HU, W., KASHGARI, G., LIN, Z., NGUYEN, T., DOAN, M. and ANDERSEN, B. (2017) Characterization of enhancers and the role of the transcription factor KLF7 in regulating corneal epithelial differentiation. Journal of Biological Chemistry 292: 18937-18950.Google Scholar
LANDROCK, D., MILLIGAN, S., MARTIN, G.G., MCLNTOSH, A.L., LANDROCK, K.K., SCHROEDER, F. and KIER, A.B. (2017) Effect of Fabp1/Scp-2/Scp-x Ablation on Whole Body and Hepatic Phenotype of Phytol-Fed Male Mice. Lipids 52: 385-397.Google Scholar
LEE, J.E. and GE, K. (2014) Transcriptional and epigenetic regulation of PPARgamma expression during Adipogenesis. Cell and Bioscience 4: 29.Google Scholar
LAY, L.S., LEFRÈRE, I., TRAUTWEIN, C., DUGAIL, I. and KRIEF, S. (2002) Insulin and sterol-regulatory element-binding protein-1c (SREBP-1C) regulation of gene expression in 3T3-L1 adipocytes: Identification of CCAAT/enhancer-binding protein beta as an SREBP-1C target. Journal of Biological Chemistry 277: 35625-35634.Google Scholar
LIN, R.L., CHEN, H.P., ROUVIER, R. and MARIE-ETANCELIN, C. (2016) Genetic parameters of body weight, egg production, and shell quality traits in the Shan Ma laying duck. Poultry Science 95: 2514-2519.Google Scholar
LIU, S., WANG, Y., WANG, L., WANG, N., LI, Y. and LI, H. (2010) Transdifferentiation of fibroblasts into adipocyte-like cells by chicken adipogenic transcription factors. Comparative Biochemistry and Physiology A-molecular & Integrative Physiology 156: 502-508.Google Scholar
MATSUBARA, Y., AOKI, M., ENDO, T. and SATO, K. (2013) Characterization of the expression profiles of adipogenesis-related factors, ZNF423, KLFs and FGF10, during preadipocyte differentiation and abdominal adipose tissue development in chickens. Bioscience Biotechnology and Biochemistry 165: 189-195.Google Scholar
MATSUBARA, Y., ENDO, T. and KANO, K. (2008) Fatty acids but not dexamethasone are essential inducers for chick adipocyte differentiation in vitro. Comparative Biochemistry and Physiology A-molecular & Integrative Physiology 151: 511-518.Google Scholar
MATSUBARA, Y., SATO, K., ISHII, H. and AKIBA, Y. (2005) Changes in mRNA expression of regulatory factors involved in adipocyte differentiation during fatty acid induced adipogenesis in chicken. Comparative Biochemistry and Physiology A-molecular & Integrative Physiology 141: 108-115.Google Scholar
MOTA, S.P., RICHARD, A.J., HANG, H. and STEPHENS, J.M. (2017) Transcriptional Regulation of Adipogenesis. Comprehensive Physiology 7: 635-674.Google Scholar
ROSEN, E.D., HSU, C.H., WANG, X., SAKAI, S., FREEMAN, M.W., GONZALEZ, F.J. and SPIEGELMAN, B.M. (2002) C/EBPalpha induces adipogenesis through PPARgamma: a unified pathway. Genes & Development 16: 22-26.Google Scholar
QI, R., FENG, M., TAN, X., GAN, L., YAN, G. and SUN, C. (2013) FATP1 silence inhibits the differentiation and induces the apoptosis in chicken preadipocytes. Molecular Biology Reports 40: 2907-2914.Google Scholar
SHANG, Z., GUO, L., WANG, N., SHI, H., WANG, Y. and LI, H. (2014) Oleate promotes differentiation of chicken primary preadipocytes in vitro. Bioscience Reports 34: 51-57.Google Scholar
SHI, H., WANG, Q., WANG, Y., LENG, L., ZHANG, Q., SHANG, Z. and LI, H. (2010) Adipocyte fatty acid-binding protein: an important gene related to lipid metabolism in chicken adipocytes. Comparative Biochemistry and Physiology B-biochemistry & Molecular Biology 157: 357-363.Google Scholar
SHIPP, S.L., CLINE, M.A. and GILBERT, E.R. (2016) Promotion of adipogenesis by neuropeptide Y during the later stages of chicken preadipocyte differentiation. Physiological Reports 4: e13006.Google Scholar
SMITH, U. and KAHN, B.B. (2016) Adipose tissue regulates insulin sensitivity: role of adipogenesis, de novo lipogenesis and novel lipids. Journal of Internal Medicine 280: 465-475.Google Scholar
SONG, Z., CHENG, J., YANG, H., LI, Y., GAO, Q., SHI, X. and YANG, G. (2015) Differentiation of 3T3‐L1 preadipocytes is inhibited under a modified ceiling culture. Cell Biology International 39: 638-645.Google Scholar
TONTONOZ, P. and SPIEGELMAN, B.M. (2008) Fat and beyond: the diverse biology of PPARgamma. Annual Review of Biochemistry 77: 289-312.Google Scholar
WANG, G., KIM, W.K., CLINE, M.A. and GILBERT, E.R. (2017a) Factors affecting adipose tissue development in chickens: A review. Poultry Science 96: 3687-3699.Google Scholar
WANG, L., LI, X., MA, J., ZHANG, Y. and ZHANG, H. (2017b) Integrating genome and transcriptome profiling for elucidating the mechanism of muscle growth and lipid deposition in Pekin ducks. Scientific Reports 7: 3837.Google Scholar
WANG, L., NA, W., WANG, Y.X., WANG, Y.B., WANG, N., WANG, Q.G., LI, Y.M. and LI, H. (2012) Characterization of chicken PPARgamma expression and its impact on adipocyte proliferation and differentiation. Yi Chuan 34: 454-464.Google Scholar
WITTE, N., MUENZNER, M., RIETSCHER, J., KNAUER, M., HEIDENREICH, S., NUOTIO-ANTAR, A.M., GRAEF, F.A., FEDDERS, R., TOLKACHOV, A., GOEHRING, I. and SCHUPP, M. (2015) The glucose sensor ChREBP links de novo lipogenesis to PPARgamma activity and adipocyte differentiation. Endocrinology156: 4008-4019.Google Scholar
XIE, W., HAMILTON, J.A., KIRKLAND, J.L., CORKEY, B.E. and GUO, W. (2006) Oleate-induced formation of fat cells with impaired insulin sensitivity. Lipids 41: 267-271.Google Scholar
XIONG, M., LI, S., PENG, X., FENG, Y., YU, G., XIN, Q. and GONG, Y. (2010) Adipogenesis in ducks interfered by small interfering ribonucleic acids of peroxisome proliferator-activated receptor gamma gene. Poultry Science 89: 88-95.Google Scholar
YAN, J., YANG, H., GAN, L. and SUN, C. (2014) Adiponectin-impaired adipocyte differentiation negatively regulates fat deposition in chicken. Journal of Animal Physiology and Animal Nutrition 98: 530-537.Google Scholar
YUE, Y., ZHANG, L., ZHANG, X., LI, X. and YU, H. (2018) De novo lipogenesis and desaturation of fatty acids during adipogenesis in bovine adipose-derived mesenchymal stem cells. In Vitro Cellular & Developmental Biology-animal 54: 23-31.Google Scholar
ZHANG, T., ZHANG, X., HAN, K., ZHANG, G., WANG, J., XIE, K. and XUE, Q. (2017a) Genome-wide analysis of lncRNA and mRNA expression during differentiation of abdominal preadipocytes in the chicken. G3-Genes Genomes Genetics 7: 953-966.Google Scholar
ZHANG, T., ZHANG, X., HAN, K., ZHANG, G., WANG, J., XIE, K., XUE, Q. and FAN, X. (2017b) Analysis of long noncoding RNA and mRNA using RNA sequencing during the differentiation of intramuscular preadipocytes in chicken. PloS One 12: e0172389.Google Scholar
ZHANG, X.Y., WU, M.Q., WANG, S.Z., ZHANG, H., DU, Z.Q., LI, Y.M., CAO, Z.P., LUAN, P., LENG, L. and LI, H. (2017c) Genetic selection on abdominal fat content alters the reproductive performance of broilers. Animal 12: 1232-1241.Google Scholar
ZHANG, Z., WANG, H., SUN, Y., LI, H. and WANG, N. (2013) Klf7 modulates the differentiation and proliferation of chicken preadipocyte. Acta Biochimica et Biophysica Sinica 45: 280-288.Google Scholar
ZHANG, Z.W., RONG, E.G., SHI, M.X., WU, C.Y., SUN, B., WANG, Y.X., WANG, N. and LI, H. (2014a) Expression and functional analysis of Kruppel-like factor 2 in chicken adipose tissue. Journal of Animal Science 92: 4797-4805.Google Scholar
ZHANG, Z.W., WU, C.Y., LI, H. and WANG, N. (2014b) Expression and functional analyses of Kruppel-like factor 3 in chicken adipose tissue. Bioscience Biotechnology and Biochemistry 78: 614-623.Google Scholar