Apolipoprotein H: a novel regulator of fat accumulation in duck myoblasts |
Ziyi, Pan
(College of Animal Science and Technology, Anhui Agricultural University)
Guoqing, Du (College of Animal Science and Technology, Anhui Agricultural University) Guoyu, Li (College of Animal Science and Technology, Anhui Agricultural University) Dongsheng, Wu (College of Animal Science and Technology, Anhui Agricultural University) Xingyong, Chen (College of Animal Science and Technology, Anhui Agricultural University) Zhaoyu, Geng (College of Animal Science and Technology, Anhui Agricultural University) |
1 | Xing S, Liu R, Zhao G, Liu L, Groenen MAM, Madsen O, et al. RNA-seq analysis reveals hub genes involved in chicken intramuscular fat and abdominal fat deposition during development. Front Genet. 2020;11:1009. https://doi.org/10.3389/fgene.2020.01009 DOI |
2 | Ye Y, Lin S, Mu H, Tang X, Ou Y, Chen J, et al. Analysis of differentially expressed genes and signaling pathways related to intramuscular fat deposition in skeletal muscle of sex-linked dwarf chickens. BioMed Res Int. 2014;2014:724274. https://doi.org/10.1155/2014/724274 DOI |
3 | Qiu F, Xie L, Ma J, Luo W, Zhang L, Chao Z, et al. Lower expression of SLC27A1 enhances intramuscular fat deposition in chicken via down-regulated fatty acid oxidation mediated by CPT1A. Front Physiol. 2017;8:449. https://doi.org/10.3389/fphys.2017.00449 DOI |
4 | Guo Y, Guo X, Deng Y, Cheng L, Hu S, Liu H, et al. Effects of different rearing systems on intramuscular fat content, fatty acid composition, and lipid metabolism-related genes expression in breast and thigh muscles of Nonghua ducks. Poult Sci. 2020;99:4832-44. https://doi.org/10.1016/j.psj.2020.06.073 DOI |
5 | Stein O, Stein Y, Lefevre M, Roheim PS. The role of apolipoprotein A-IV in reverse cholesterol transport studied with cultured cells and liposomes derived from an ether analog of phosphatidylcholine. Biochim Biophys Acta Mol Cell Biol Lipids. 1986;878:7-13. https://doi.org/10.1016/0005-2760(86)90337-1 DOI |
6 | George J, Harats D, Gilburd B, Afek A, Levy Y, Schneiderman J, et al. Immunolocalization of β2-glycoprotein I (apolipoprotein H) to human atherosclerotic plaques: potential implications for lesion progression. Circulation. 1999;99:2227-30. https://doi.org/10.1161/01.CIR.99.17.2227 DOI |
7 | Afek A, George J, Shoenfeld Y, Gilburd B, Levy Y, Shaish A, et al. Enhancement of atherosclerosis in beta-2-glycoprotein I-immunized apolipoprotein E-deficient mice. Pathobiology. 1999;67:19-25. https://doi.org/10.1159/000028046 DOI |
8 | Tsonkova VG, Sand FW, Wolf XA, Grunnet LG, Ringgaard AK, Ingvorsen C, et al. The EndoC-βH1 cell line is a valid model of human beta cells and applicable for screenings to identify novel drug target candidates. Mol Metab. 2018;8:144-57. https://doi.org/10.1016/j.molmet.2017.12.007 DOI |
9 | Perrin RJ, Craig-Schapiro R, Malone JP, Shah AR, Gilmore P, Davis AE, et al. Identification and validation of novel cerebrospinal fluid biomarkers for staging early Alzheimer's disease. PLOS ONE. 2011;6:e16032. https://doi.org/10.1371/journal.pone.0016032 DOI |
10 | Hoekstra M, Chen HY, Rong J, Dufresne L, Yao J, Guo X, et al. Genome-wide association study highlights APOH as a novel locus for lipoprotein(a) levels-brief report. Arterioscler Thromb Vasc Biol. 2021;41:458-64. https://doi.org/10.1161/ATVBAHA.120.314965 DOI |
11 | Song F, Poljak A, Crawford J, Kochan NA, Wen W, Cameron B, et al. Plasma apolipoprotein levels are associated with cognitive status and decline in a community cohort of older individuals. PLOS ONE. 2012;7:e34078. https://doi.org/10.1371/journal.pone.0034078 DOI |
12 | Nakaya Y, Schaefer EJ, Brewer HB Jr. Activation of human post heparin lipoprotein lipase by apolipoprotein H (β2-glycoprotein I). Biochem Biophys Res Commun. 1980;95:1168-72. https://doi.org/10.1016/0006-291x(80)91595-8 DOI |
13 | Schousboe I. Binding of β2-glycoprotein I to platelets: effect of adenylate cyclase activity. Thromb Res. 1980;19:225-37. https://doi.org/10.1016/0049-3848(80)90421-1 DOI |
14 | Nimpf J, Bevers EM, Bomans PHH, Till U, Wurm H, Kostner GM, et al. Prothrombinase activity of human platelets is inhibited by β2-glycoprotein-I. Biochim Biophys Acta Gen Subj. 1986;884:142-9. https://doi.org/10.1016/0304-4165(86)90237-0 DOI |
15 | Sha H, Sun S, Francisco AB, Ehrhardt N, Xue Z, Liu L, et al. The ER-associated degradation adaptor protein Sel1L regulates LPL secretion and lipid metabolism. Cell Metabol. 2014;20:458-70. https://doi.org/10.1016/j.cmet.2014.06.015 DOI |
16 | He C, Zhang G, Ouyang H, Zhang P, Chen Y, Wang R, et al. Effects of β2/aβ2 on oxLDLinduced CD36 activation in THP-1 macrophages. Life Sci. 2019;239:117000. https://doi.org/10.1016/j.lfs.2019.117000 DOI |
17 | Yagyu H, Chen G, Yokoyama M, Hirata K, Augustus A, Kako Y, et al. Lipoprotein lipase (LpL) on the surface of cardiomyocytes increases lipid uptake and produces a cardiomyopathy. J Clin Invest. 2003;111:419-26. https://doi.org/doi.org/10.1172/JCI16751 DOI |
18 | Yuan SM, Guo Y, Wang Q, Xu Y, Wang M, Chen HN, et al. Over-expression of PPAR-γ2 gene enhances the adipogenic differentiation of hemangioma-derived mesenchymal stem cells in vitro and in vivo. Oncotarget. 2017;8:115817-28. https://doi.org/10.18632/oncotarget.23705 DOI |
19 | Zhong J, Gong W, Lu L, Chen J, Lu Z, Li H, et al. Irbesartan ameliorates hyperlipidemia and liver steatosis in type 2 diabetic db/db mice via stimulating PPAR-γ, AMPK/Akt/mTOR signaling and autophagy. Int Immunopharmacol. 2017;42:176-84. https://doi.org/10.1016/j.intimp.2016.11.015 DOI |
20 | Chawla A, Barak Y, Nagy L, Liao D, Tontonoz P, Evans RM. PPAR-γ dependent and independent effects on macrophage-gene expression in lipid metabolism and inflammation. Nat Med. 2001;7:48-52. https://doi.org/10.1038/83336 DOI |
21 | Guo L, Cui H, Zhao G, Liu R, Li Q, Zheng M, et al. Intramuscular preadipocytes impede differentiation and promote lipid deposition of muscle satellite cells in chickens. BMC Genomics. 2018;19:838. https://doi.org/10.1186/s12864-018-5209-5 DOI |
22 | Jin S, Xu Y, Zang H, Yang L, Lin Z, Li Y, et al. Expression of genes related to lipid transport in meat-type ducks divergent for low or high residual feed intake. Asian-Australas J Anim Sci. 2020;33:416-23. https://doi.org/10.5713/ajas.19.0284 DOI |
23 | Machann J, Haring H, Schick F, Stumvoll M. Intramyocellular lipids and insulin resistance. Diabetes Obes Metab. 2004;6:239-48. https://doi.org/10.1111/j.1462-8902.2004.00339.x DOI |
24 | Xu S, Huang Y, Xie Y, Lan T, Le K, Chen J, et al. Evaluation of foam cell formation in cultured macrophages: an improved method with Oil Red O staining and DiI-oxLDL uptake. Cytotechnology. 2010;62:473-81. https://doi.org/10.1007/s10616-010-9290-0 DOI |
25 | Shaw CS, Clark J, Wagenmakers AJM. The effect of exercise and nutrition on intramuscular fat metabolism and insulin sensitivity. Annu Rev Nutr. 2010;30:13-34. https://doi.org/10.1146/annurev.nutr.012809.104817 DOI |
26 | Mihaylova MM, Shaw RJ. The AMPK signalling pathway coordinates cell growth, autophagy and metabolism. Nat Cell Biol. 2011;13:1016-23. https://doi.org/10.1038/ncb2329 DOI |
27 | Moro C, Bajpeyi S, Smith SR. Determinants of intramyocellular triglyceride turnover: implications for insulin sensitivity. Am J Physiol Endocrinol Metab. 2008;294:E203-13. https://doi.org/10.1152/ajpendo.00624.2007 DOI |
28 | Jacobsen SC, Brons C, Bork-Jensen J, Ribel-Madsen R, Yang B, Lara E, et al. Effects of shortterm high-fat overfeeding on genome-wide DNA methylation in the skeletal muscle of healthy young men. Diabetologia. 2012;55:3341-9. https://doi.org/10.1007/s00125-012-2717-8 DOI |
29 | Liu J, Fu R, Liu R, Zhao G, Zheng M, Cui H, et al. Protein profiles for muscle development and intramuscular fat accumulation at different post-hatching ages in chickens. PLOS ONE. 2016;11:e0159722. https://doi.org/10.1371/journal.pone.0159722 DOI |
30 | Reyer H, Metzler-Zebeli BU, Trakooljul N, Oster M, Murani E, Ponsuksili S, et al. Transcriptional shifts account for divergent resource allocation in feed efficient broiler chickens. Sci Rep. 2018;8:12903. https://doi.org/10.1038/s41598-018-31072-7 DOI |
31 | Tyszka-Czochara M, Konieczny P, Majka M. Recent advances in the role of AMP-activated protein kinase in metabolic reprogramming of metastatic cancer cells: targeting cellular bioenergetics and biosynthetic pathways for anti-tumor treatment. J Physiol Pharmacol. 2018;69:337-49. https://doi.org/10.26402/jpp.2018.3.07 DOI |
32 | Castro A, Lazaro I, Selva DM, Cespedes E, Girona J, Plana N, et al. APOH is increased in the plasma and liver of type 2 diabetic patients with metabolic syndrome. Atherosclerosis. 2010;209:201-5. https://doi.org/10.1016/j.atherosclerosis.2009.09.072 DOI |
33 | Wang X, Li Y, Chen X, Zhou Z, Yao J. Human acetyl-CoA carboxylase 1 is an isomerase: carboxyl transfer is activated by catalytic effect of isomerization. J Phys Chem B. 2019;123:6757-64. https://doi.org/10.1021/acs.jpcb.9b05384 DOI |
34 | Fullerton MD, Galic S, Marcinko K, Sikkema S, Pulinilkunnil T, Chen ZP, et al. Single phosphorylation sites in Acc1 and Acc2 regulate lipid homeostasis and the insulin-sensitizing effects of metformin. Nat Med. 2013;19:1649-54. https://doi.org/10.1038/nm.3372 DOI |
35 | Du C, Wu M, Liu H, Ren Y, Du Y, Wu H, et al. Thioredoxin-interacting protein regulates lipid metabolism via Akt/mTOR pathway in diabetic kidney disease. Int J Biochem Cell Biol. 2016;79:1-13. https://doi.org/10.1016/j.biocel.2016.08.006 DOI |
36 | Habinowski SA, Witters LA. The effects of AICAR on adipocyte differentiation of 3T3-L1 cells. Biochem Biophys Res Commun. 2001;286:852-6. https://doi.org/10.1006/bbrc.2001.5484 DOI |
37 | Jiang T, Shi X, Yan Z, Wang X, Gun S. Isoimperatorin enhances 3T3-L1 preadipocyte differentiation by regulating PPARγ and C/EBPα through the Akt signaling pathway. Exp Ther Med. 2019;18:2160-6. https://doi.org/10.3892/etm.2019.7820 DOI |
38 | Yan G, Li X, Peng Y, Long B, Fan Q, Wang Z, et al. The fatty acid β-oxidation pathway is activated by leucine deprivation in HepG2 cells: a comparative proteomics study. Sci Rep. 2017;7:1914. https://doi.org/10.1038/s41598-017-02131-2 DOI |
39 | Li T, Li X, Meng H, Chen L, Meng F. ACSL1 affects triglyceride levels through the PPARγ pathway. Int J Med Sci. 2020;17:720-7. https://doi.org/10.7150/ijms.42248 DOI |
40 | Singh AB, Kan CFK, Dong B, Liu J. SREBP2 activation induces hepatic long-chain acyl-CoA synthetase 1 (ACSL1) expression in vivo and in vitro through a sterol regulatory element (SRE) motif of the ACSL1 C-promoter. J Biol Chem. 2016;291:5373-84. https://doi.org/10.1074/jbc.m115.696872 DOI |
41 | Manning BD, Toker A. AKT/PKB signaling: navigating the network. Cell. 2017;169:381-405. https://doi.org/10.1016/j.cell.2017.04.001 DOI |
42 | Peng X, Chen R, Wu Y, Huang B, Tang C, Chen J, et al. PPARγ-PI3K/AKT-NO signal pathway is involved in cardiomyocyte hypertrophy induced by high glucose and insulin. J Diabetes Complications. 2015;29:755-60. https://doi.org/10.1016/j.jdiacomp.2015.04.012 DOI |
43 | Bermudez B, Dahl TB, Medina I, Groeneweg M, Holm S, Montserrat-de la Paz S, et al. Leukocyte overexpression of intracellular NAMPT attenuates atherosclerosis by regulating PPARγ-dependent monocyte differentiation and function. Arterioscler Thromb Vasc Biol. 2017;37:1157-67. https://doi.org/10.1161/ATVBAHA.116.308187 DOI |
44 | Goudriaan JR, Espirito Santo SM, Voshol PJ, Teusink B, van Dijk KW, van Vlijmen BJM, et al. The VLDL receptor plays a major role in chylomicron metabolism by enhancing LPLmediated triglyceride hydrolysis. J Lipid Res. 2004;45:1475-81. https://doi.org/10.1194/jlr.M400009-JLR200 DOI |
45 | Sunaga H, Matsui H, Anjo S, Syamsunarno MRAA, Koitabashi N, Iso T, et al. Elongation of long-chain fatty acid family member 6 (Elovl6)-driven fatty acid metabolism regulates vascular smooth muscle cell phenotype Tthrough AMP-activated protein kinase/Kruppel-like factor 4 (AMPK/KLF4) signaling. J Am Heart Assoc. 2016;5:e004014. https://doi.org/10.1161/JAHA.116.004014 DOI |
46 | Matsuzaka T, Shimano H. Elovl6: a new player in fatty acid metabolism and insulin sensitivity. J Mol Med. 2009;87:379-84. https://doi.org/10.1007/s00109-009-0449-0 DOI |
47 | Fan X, Zhu W, Qiu L, Zhang G, Zhang Y, Miao Y. Elongase of very long chain fatty acids 6 (ELOVL6) promotes lipid synthesis in buffalo mammary epithelial cells. J Anim Physiol Anim Nutr. 2022;106:1-11. https://doi.org/10.1111/jpn.13536 DOI |
48 | Matsuzaka T, Atsumi A, Matsumori R, Nie T, Shinozaki H, Suzuki-Kemuriyama N, et al. Elovl6 promotes nonalcoholic steatohepatitis. Hepatology. 2012;56:2199-208. https://doi.org/10.1002/hep.25932 DOI |