Abstract
The relationship between obesity and coronary artery disease (CAD) may be mediated by epicardial adipose tissue (EAT). EAT volume correlates with abdominal visceral adipose tissue and as a consequence EAT is increased in patients with obesity. The presence of EAT adjacent to the coronary atherosclerotic lesions suggests a paracrine participation of this tissue in the progression and calcification of the atheroma. EAT expresses cardioprotective adipocytokines and anti-calcifying factors, such as adiponectin and osteoprotegerin among others, whose expression declines in the setting of a hypertrophy of the EAT and CAD. In contrast, pro-inflammatory and pro-calcifying molecules such as TNF-alpha, and osteopontin, as well as some microRNAs, are expressed in a higher amount in patients with CAD than in control subjects. Therefore, the quantification of the EAT emerges as a potential and useful determination for evaluating the CAD risk. However, the understanding of the complexity of the secretory pattern of EAT is still under investigation; the knowledge derived from future studies in this field will provide new potential pharmacological targets to prevent and treat the CAD.
Access this chapter
Tax calculation will be finalised at checkout
Purchases are for personal use only
References
Esteve RM (2014) Adipose tissue: cell heterogeneity and functional diversity. Endocrinol Nutr 61:100–112
van Dam AD, Boon MR, Berbée JFP et al (2017) Targeting white, brown and perivascular adipose tissue in atherosclerosis development. Eur J Pharmacol 816:82–92
Alexopoulos N, Katritsis D, Raggi P (2014) Visceral adipose tissue as a source of inflammation and promoter of atherosclerosis. Atherosclerosis 233:104–112
Lin, Chun TH, Kang L (2016) Adipose extracellular matrix remodelling in obesity and insulin resistance. Biochem Pharmacol 119:8–16
Luo T, Nocon A, Fry J et al (2016) AMPK activation by metformin suppresses abnormal extracellular matrix remodeling in adipose tissue and ameliorates insulin resistance in obesity. Diabetes 65:2295–2310
Fox CS, Massaro JM, Hoffmann U et al (2007) Abdominal visceral and subcutaneous adipose tissue compartments: association with metabolic risk factors in the Framingham Heart Study. Circulation 116:39–48
Boon MR, van Marken Lichtenbelt WD (2016) Brown adipose tissue: a human perspective. Handb Exp Pharmacol 233:301–319
Song NJ, Chang SH, Li DY et al (2017) Induction of thermogenic adipocytes: molecular targets and thermogenic small molecules. Exp Mol Med 49:e353
Saito M (2014) Human brown adipose tissue: regulation and anti- obesity potential. Endocr J 61:409–416
Lidel ME, Betz MJ, Enerbäck S (2014) Brown adipose tissue and its therapeutic potential. J Intern Med 276:364–377
Cui XB, Chen SY (2016) White adipose tissue browning and obesity. J Biomed Res 31:1–2
Kiefer FW (2016) Browning and thermogenic programing of adipose tissue. Best Pract Res Clin Endocrinol Metab 30:479–485
Jeanson Y, Carrière A, Casteilla L (2015) A new role for browning as a redox and stress adaptive mechanism? Front Endocrinol (Lausanne) 6:158
Luna-Luna M, Medina-Urrutia A, Vargas-Alarcón G et al (2015) Adipose tissue in metabolic syndrome: onset and progression of atherosclerosis. Arch Med Res 46:392–407
Trayhurn P (2013) Hypoxia and adipose tissue function and dysfunction in obesity. Physiol Rev 93:1–21
Yamamoto A, Kikuchi Y, Kusakabe T et al (2020) Imaging spectrum of abnormal subcutaneous and visceral fat distribution. Insights Imaging 11:24
Passaro A, Miselli MA, Sanz JM et al (2017) Gene expression regional differences in human subcutaneous adipose tissue. BMC Genomics 18:202
Iacobellis G (2009) Epicardial and pericardial fat: close, but very different. Obesity (Silver Spring) 17:625
Chhabra L, Gurukripa KN (2015) Cardiac adipose tissue: distinction between epicardial and pericardial fat remains important! Int J Cardiol 201:274–275
Chau YY, Bandiera R, Serrels A et al (2014) Visceral and subcutaneous fat have different origins and evidence supports a mesothelial source. Nat Cell Biol 16:367–375
Gupta OT, Gupta RK (2015) Visceral adipose tissue mesothelial cells: living on the edge or just taking up space? Trends Endocrinol Metab 26:515–523
Sebo ZL, Jeffery E, Holtrup B, Rodeheffer MS (2018) A mesodermal fate map for adipose tissue. Development 145:dev166801
Jové M, Moreno-Navarrete JM, Pamplona R et al (2014) Human omental and subcutaneous adipose tissue exhibit specific lipidomic signatures. FASEB J 28:1071–1081
Fuster JJ, Ouchi N, Gokce N, Walsh K (2016) Obesity-induced changes in adipose tissue microenvironment and their impact on cardiovascular disease. Circ Res 118:1786–1807
Zhang C, Rexrode KM, van Dam RM et al (2008) Abdominal obesity and the risk of all-cause, cardiovascular, and cancer mortality: sixteen years of follow-up in US women. Circulation 117:1658–1667
Pinho CPS, Diniz ADS, Arruda IKG et al (2018) Waist circumference measurement sites and their association with visceral and subcutaneous fat and cardiometabolic abnormalities. Arch Endocrinol Metab 62:416–423
Sun Q, Townsend MK, Okereke OI et al (2009) Adiposity and weight change in mid-life in relation to healthy survival after age 70 in women: prospective cohort study. BMJ 339:b3796
Rallidis LS, Baroutsi K, Zolindaki M et al (2014) Visceral adipose tissue is a better predictor of subclinical carotid atherosclerosis compared with waist circumference. Ultrasound Med Biol 40:1083–1088
Prospective Studies Collaboration, Whitlock G, Lewington S et al (2009) Body-mass index and cause-specific mortality in 900 000 adults: collaborative analyses of 57 prospective studies. Lancet 373:1083–1096
Wu FZ, Wu CC, Kuo PL, Wu MT (2016) Differential impacts of cardiac and abdominal ectopic fat deposits on cardiometabolic risk stratification. BMC Cardiovasc Disord 16:20
Chistiakov DA, Grechko AV, Myasoedova VA et al (2017) Impact of the cardiovascular system-associated adipose tissue on atherosclerotic pathology. Atherosclerosis 263:361–368
Patel VB, Shah S, Verma S, Oudit GY (2017) Epicardial adipose tissue as a metabolic transducer: role in heart failure and coronary disease. Heart Fail Rev 22:889–902
Iacobellis G (2015) Local and system effects of the multifaceted epicardial adipose tissue depot. Nat Rev Endocrinol 11:363–371
González N, Moreno-Villegas Z, González-Bris A et al (2017) Regulation of visceral and epicardial adipose tissue for preventing cardiovascular injuries associated to obesity and diabetes. Cardiovasc Diabetol 16:44
Gaborit B, Sengenes C, Ancel P et al (2017) Role of epicardial adipose tissue in health and disease: a matter of fat? Compr Physiol 7:1051–1082
Sacks HS, Fain JN (2011) Human epicardial fat: what is new and what is missing? Clin Exp Pharmacol Physiol 38:879–887
Iacobellis G, Assael F, Ribaudo MC et al (2003) Epicardial fat from echocardiography a new method for visceral adipose tissue prediction. Obes Res 11:304–310
Sacks HS, Fain JN (2007) Human epicardial adipose tissue: a review. Am Heart J 153:907–917
Bambace C, Telesca M, Zoico E et al (2011) Adiponectin gene expression and adipocyte diameter: a comparison between epicardial and subcutaneous adipose tissue in men. Cardiovasc Pathol 20:e153–e156
Iacobellis G, Bianco AC (2011) Epicardial adipose tissue: emerging physiological, pathophysiological and clinical features. Trends Endocrinol Metab 22:450–457
Cherian S, Lopaschuk GD, Carvalho E (2012) Cellular cross-talk between epicardial adipose tissue and myocardium in relation to the pathogenesis of cardiovascular disease. Am J Physiol Endocrinol Metab 303:E937–E949
Sacks HS, Fain JN, Holman B et al (2009) Uncoupling protein-1 and related messenger ribonucleic acids in human epicardial and other adipose tissues: epicardial fat functioning as brown fat. J Clin Endocrinol Metab 94:3611–3615
Silaghi A, Piercecchi-Marti MD, Grino M et al (2008) Epicardial adipose tissue extent: relationship with age, body fat distribution, and coronaropathy. Obesity (Silver Spring) 16:2424–2430
de Feyter PJ (2011) Epicardial adipose tissue: an emerging role for the development of coronary atherosclerosis. Clin Cardiol 34:143–144
de Vos AM, Prokop M, Roos CJ et al (2008) Peri-coronary epicardial adipose tissue is related to cardiovascular risk factors and coronary artery calcification in post-menopausal women. Eur Heart J 29:777–783
Ueno K, Anzai T, Jinzaki M et al (2009) Increased epicardial fat volume quantified by 64-multidetector computed tomography is associated with coronary atherosclerosis and totally occlusive lesions. Circ J 73:1927–1933
Xu Y, Cheng X, Hong K et al (2012) How to interpret epicardial adipose tissue as a cause of coronary artery disease: a meta-analysis. Coron Artery Dis 23:227–233
McKenney ML, Schultz KA, Boyd JH, Byrd JP et al (2014) Epicardial adipose excision slows the progression of porcine coronary atherosclerosis. J Cardiothorac Surg 9:2
Iacobellis G, Barbaro G (2008) The double role of epicardial adipose tissue as pro- and anti-inflammatory organ. Horm Metab Res 40:442–445
Cheng KH, Chu CS, Lee KT et al (2008) Adipocytokines and proinflammatory mediators from abdominal and epicardial adipose tissue in patients with coronary artery disease. Int J Obes 32:268–274
Hirata Y, Kurobe H, Akaike M et al (2011) Enhanced inflammation in epicardial fat in patients with coronary artery disease. Int Heart J 52:139–142
Creely SJ, McTernan PG, Kusminski CM et al (2007) Lipopolysaccharide activates an innate immune system response in human adipose tissue in obesity and type 2 diabetes. Am J Physiol Endocrinol Metab. 292:E740–E747
Baker AR, Harte AL, Howell N et al (2009) Epicardial adipose tissue as a source of nuclear factor kappa B and c-Jun N-terminal kinase mediated inflammation in patients with coronary artery disease. J Clin Endocrinol Metab 94:261–267
Cesari M, Pessina AC, Zanchetta M et al (2006) Low plasma adiponectin is associated with coronary artery disease but not with hypertension in high-risk nondiabetic patients. J Intern Med 260:474–483
Iacobellis G, Pistilli D, Gucciardo M et al (2005) Adiponectin expression in human epicardial adipose tissue in vivo is lower in patients with CAD. Cytokine 29:251–255
Dutour A, Achard V, Sell H et al (2010) Secretory type II phospholipase A2 is produced and secreted by epicardial adipose tissue and over expressed in patients with CAD. J Clin Endocrinol Metab 95:963–967
Watanabe K, Watanabe R, Konii H et al (2016) Counteractive effects of omentin-1 against atherogenesis†. Cardiovasc Res 110:118–128
Du Y, Ji Q, Cai L et al (2016) Association between omentin-1 expression in human epicardial adipose tissue and coronary atherosclerosis. Cardiovasc Diabetol 15:90
Moreno-Santos I, Pérez-Belmonte LM, Macías-González M et al (2016) Type 2 diabetes is associated with decreased PGC1α expression in epicardial adipose tissue of patients with coronary artery disease. J Transl Med 14:243
Uldry M, Yang W, St-Pierre J et al (2006) Complementary action of the PGC1 coactivators in mitochondrial biogenesis and brown fat differentiation. Cell Metab 3:333–341
Hisamatsu T, Fujiyoshi A, Miura K (2019) Coronary artery calcium: its clinical utility in primary prevention. Clin Calcium 29:215–223
Erbel R, Möhlenkamp S, Moebus S et al (2010) Coronary risk stratification, discrimination, and reclassification improvement based on quantification of subclinical coronary atherosclerosis: the Heinz Nixdorf Recall study. J Am Coll Cardiol 56:1397–1406
Erbel R, Lehmann N, Churzidse S et al (2013) Gender-specific association of coronary artery calcium and lipoprotein parameters: the Heinz Nixdorf Recall Study. Atherosclerosis 229:531–540
García-Sánchez C, Posadas-Romero C, Posadas-Sánchez R et al (2015) Low concentrations of phospholipids and plasma HDL cholesterol subclasses in asymptomatic subjects with high coronary calcium scores. Atherosclerosis 238:250–255
Iwasaki K, Matsumoto T, Aono H et al (2011) Relationship between epicardial fat measured by 64-multidetector computed tomography and coronary artery disease. Clin Cardiol 34:166–171
Djaberi R, Schuijf JD, van Werkhoven JM et al (2008) Relation of epicardial adipose tissue to coronary atherosclerosis. Am J Cardiol 102:1602–1607
Kim BJ, Kang JG, Lee SH et al (2017) Relationship of echocardiographic epicardial fat thickness and epicardial fat volume by computed tomography with coronary artery calcification: data from the CAESAR Study. Arch Med Res. 48:352–359
Iwasaki K, Urabe N, Kitagawa A, Nagao T (2018) The association of epicardial fat volume with coronary characteristics and clinical outcome. Int J Cardiovasc Imaging 34:301–309
Yerramasu A, Dey D, Venuraju S et al (2012) Increased volume of epicardial fat is an independent risk factor for accelerated progression of sub-clinical coronary atherosclerosis. Atherosclerosis 220:223–230
Isoda K, Nishikawa K, Kamezawa Y et al (2002) Osteopontin plays an important role in the development of medial thickening and neointimal formation. Circ Res 91:77–782
Hirota S, Imakita M, Kohri K et al (1993) Expression of osteopontin messenger RNA by macrophages in atherosclerotic plaques. A possible association with calcification. Am J Pathol 143:1003–1008
Chiba S, Okamoto H, Kon S et al (2002) Development of atherosclerosis in osteopontin transgenic mice. Heart Vessels 16:111–117
Matsui Y, Rittling SR, Okamoto H et al (2003) Osteopontin deficiency attenuates atherosclerosis in female apolipoprotein E-deficient mice. Arterioscler Thromb Vasc Biol 23:1029–1034
Jono S, Peinado C, Giachelli CM (2000) Phosphorylation of osteopontin is required for inhibition of vascular smooth muscle cell calcification. J Biol Chem 275:20197–20203
Jiménez- Corona AE, Pérez-Torres A, Mas-Oliva J, Moreno A (2008) Effect of osteopontin, chondroitin sulfates (B, C), and human serum albumin in the crystalization behavior of hydroxiapatite in agarose and silica hydrogels. Cryst Growth Des 8:1335–1339
Wolak T (2014) Osteopontin—a multi-modal marker and mediator in atherosclerotic vascular disease. Atherosclerosis 236:327–337
Liaw L, Lindner V, Schwartz SM et al (1995) Osteopontin and beta 3 integrin are coordinately expressed in regenerating endothelium in vivo and stimulate Arg-Gly-Asp-dependent endothelial migration in vitro. Circ Res 77:665–672
Miyazaki Y, Setoguchi M, Yoshida S et al (1990) The mouse osteopontin gene. Expression in monocytic lineages and complete nucleotide sequence. J Biol Chem 265:14432–14438
Giachelli CM, Bae N, Almeida M et al (1993) Osteopontin is elevated during neointima formation in rat arteries and is a novel component of human atherosclerotic plaques. J Clin Invest 92:1686–1696
O’Brien ER, Garvin MR, Stewart DK et al (1994) Osteopontin is synthesized by macrophage, smooth muscle, and endothelial cells in primary and restenotic human coronary atherosclerotic plaques. Arterioscler Thromb 14:1648–1656
Luna-Luna M, Cruz-Robles D, Ávila-Vanzzini N et al (2017) Differential expression of osteopontin, and osteoprotegerin mRNA in epicardial adipose tissue between patients with severe coronary artery disease and aortic valvular stenosis: association with HDL subclasses. Lipids Health Dis 16:156
Zeyda M, Gollinger K, Todoric J et al (2011) Osteopontin is an activator of human adipose tissue macrophages and directly affects adipocyte function. Endocrinology 152:2219–2227
Deuell KA, Callegari A, Giachelli CM et al (2012) RANKL enhances macrophage paracrine pro-calcific activity in high phosphate-treated smooth muscle cells: dependence on IL-6 and TNF-alpha. J Vasc Res 49:510–521
Tintut Y, Patel J, Parhami F, Demer LL (2000) Tumor necrosis factor-alpha promotes in vitro calcification of vascular cells via the cAMP pathway. Circulation 102:2636–2642
Csiszar A, Smith KE, Koller A et al (2005) Regulation of bone morphogenetic protein-2 expression in endothelial cells: role of nuclear factor-kappaB activation by tumor necrosis factor-alpha, H2O2, and high intravascular pressure. Circulation 111:2364–2372
Lee HL, Woo KM, Ryoo HM, Baek JH (2010) Tumor necrosis factor-alpha increases alkaline phosphatase expression in vascular smooth muscle cells via MSX2 induction. Biochem Biophys Res Commun 391:1087–1092
Csiszar A, Ahmad M, Smith KE et al (2006) Bone morphogenetic protein-2 induces proinflammatory endothelial phenotype. Am J Pathol 168:629–638
Kaden JJ, Kiliç R, Sarikoç A et al (2005) Tumor necrosis factor alpha promotes an osteoblast-like phenotype in human aortic valve myofibroblasts: a potential regulatory mechanism of valvular calcification. Int J Mol Med 16:869–872
Proudfoot D, Skepper JN, Hegyi L et al (2000) Apoptosis regulates human vascular calcification in vitro: evidence for initiation of vascular calcification by apoptotic bodies. Circ Res 87:1055–1062
Proudfoot D, Skepper JN, Hegyi L et al (2001) The role of apoptosis in the initiation of vascular calcification. Z Kardiol 90(Suppl 3):43–46
Emery JG, McDonnell P, Burke MB et al (1998) Osteoprotegerin is a receptor for the cytotoxic ligand TRAIL. J Biol Chem 273:14363–14367
Gochuico BR, Zhang J, Ma BY et al (2000) TRAIL expression in vascular smooth muscle. Am J Physiol Lung Cell Mol Physiol 278:L1045–L1050
Sato K, Niessner A, Kopecky SL et al (2006) TRAIL-expressing T cells induce apoptosis of vascular smooth muscle cells in the atherosclerotic plaque. J Exp Med 203:239–250
Bennett BJ, Scatena M, Kirk EA et al (2006) Osteoprotegerin inactivation accelerates advanced atherosclerotic lesion progression and calcification in older ApoE-/- mice. Arterioscler Thromb Vasc Biol 26:2117–2124
Morony S, Tintut Y, Zhang Z, Cattley RC, Van G, Dwyer D et al (2008) Osteoprotegerin inhibits vascular calcification without affecting atherosclerosis in ldlr(-/-) mice. Circulation 117(3):411–420
Min H, Morony S, Sarosi I et al (2000) Osteoprotegerin reverses osteoporosis by inhibiting endosteal osteoclasts and prevents vascular calcification by blocking a process resembling osteoclastogenesis. J Exp Med 192:463–474
Schoppet M, Preissner KT, Hofbauer LC (2002) RANK ligand and osteoprotegerin: paracrine regulators of bone metabolism and vascular function. Arterioscler Thromb Vasc Biol 22:549–553
Kaden JJ, Bickelhaupt S, Grobholz R et al (2004) Receptor activator of nuclear factor kappaB ligand and osteoprotegerin regulate aortic valve calcification. J Mol Cell Cardiol 36:57–66
Kanegae Y, Tavares AT, Izpisúa Belmonte JC, Verma IM (1998) Role of Rel/NF-kappaB transcription factors during the outgrowth of the vertebrate limb. Nature 392:611–614
Sun M, Chang Q, Xin M et al (2017) Endegenous bone morphogenetic protein 2 plays a role in vascular smooth musccle cell calcification induced by interleukin 6 in vitro. Int J Immunopathol Pharmacol 30:227–237
Hruska KA, Mathew S, Saab G (2005) Bone morphogenetic proteins in vascular calcification. Circ Res 97:105–114
Shimizu T, Tanaka T, Iso T et al (2011) Notch signaling pathway enhances bone morphogenetic protein 2 (BMP2) responsiveness of Msx2 gene to induce osteogenic differentiation and mineralization of vascular smooth muscle cells. J Biol Chem 286:19138–19148
Cheng SL, Shao JS, Charlton-Kachigian N et al (2003) MSX2 promotes osteogenesis and suppresses adipogenic differentiation of multipotent mesenchymal progenitors. J Biol Chem 278:45969–45977
Shao JS, Cai J, Towler DA (2006) Molecular mechanisms of vascular calcification: lessons learned from the aorta. Arterioscler Thromb Vasc Biol 26:1423–1430
Derwall M, Malhotra R, Lai CS et al (2012) Inhibition of bone morphogenetic protein signaling reduces vascular calcification and atherosclerosis. Arterioscler Thromb Vasc Biol 32:613–622
Nakagawa Y, Ikeda K, Akakabe Y et al (2010) Paracrine osteogenic signals via bone morphogenetic protein-2 accelerate the atherosclerotic intimal calcification in vivo. Arterioscler Thromb Vasc Biol 30:1908–1915
Li X, Yang HY, Giachelli CM (2008) BMP-2 promotes phosphate uptake, phenotypic modulation, and calcification of human vascular smooth muscle cells. Atherosclerosis 199:271–277
Chiyoya M, Seya K, Yu Z et al (2018) Matrix Gla protein negatively regulates calcification of human aortic valve interstitial cells isolated from calcified aortic valves. J Pharmacol Sci 136:257–265
Yao Y, Bennett BJ, Wang X et al (2010) Inhibition of bone morphogenetic proteins protects against atherosclerosis and vascular calcification. Circ Res 107:485–494
Feng J, Gao J, Li Y et al (2014) BMP4 enhances foam cell formation by BMPR-2/Smad1/5/8 signaling. Int J Mol Sci 15:5536–5552
Dhore CR, Cleutjens JP, Lutgens E et al (2001) Differential expression of bone matrix regulatory proteins in human atherosclerotic plaques. Arterioscler Thromb Vasc Biol 21:1998–2003
Panizo S, Cardus A, Encinas M et al (2009) RANKL increases vascular smooth muscle cell calcification through a RANK-BMP4-dependent pathway. Circ Res 104:1041–1048
Mikhaylova L, Malmquist J, Nurminskaya M (2007) Regulation of in vitro vascular calcification by BMP4, VEGF and Wnt3a. Calcif Tissue Int 81:372–381
Hayashi K, Nakamura S, Nishida W, Sobue K (2006) Bone morphogenetic protein-induced MSX1 and MSX2 inhibit myocardin-dependent smooth muscle gene transcription. Mol Cell Biol 26:9456–9470
Wang W, Li C, Pang L et al (2014) Mesenchymal stem cells recruited by active TGFβ contribute to osteogenic vascular calcification. Stem Cells Dev 23:1392–1404
Wan M, Li C, Zhen G et al (2012) Injury-activated transforming growth factor β controls mobilization of mesenchymal stem cells for tissue remodeling. Stem Cells 30:2498–2511
Jamaluddin MS, Weakley SM, Zhang L et al (2011) miRNAs: roles and clinical applications in vascular disease. Expert Rev Mol Diagn 11:79–89
Xia ZY, Hu Y, Xie PL et al (2015) Runx2/miR-3960/miR-2861 positive feedback loop is responsible for osteogenic transdifferentiation of vascular smooth muscle cells. Biomed Res Int 2015:624037
Sudo R, Sato F, Azechi T, Wachi H (2015) MiR-29-mediated elastin down-regulation contributes to inorganic phosphorus-induced osteoblastic differentiation in vascular smooth muscle cells. Genes Cells 20:1077–1087
Rangrez AY, M’Baya-Moutoula E, Metzinger-Le Meuth V et al (2012) Inorganic phosphate accelerates the migration of vascular smooth muscle cells: evidence for the involvement of miR-223. PLoS ONE 7:e47807
Jiang W, Zhang Z, Yang H et al (2017) The involvement of miR-29b-3p in arterial calcification by targeting matrix metalloproteinase-2. Biomed Res Int 2017:6713606
Qiao W, Chen L, Zhang M (2014) MicroRNA-205 regulates the calcification and osteoblastic differentiation of vascular smooth muscle cells. Cell Physiol Biochem 33:1945–1953
Zheng S, Zhang S, Song Y et al (2016) MicroRNA-297a regulates vascular calcification by targeting fibroblast growth factor 23. Iran J Basic Med Sci 19:1331–1336
Liao XB, Zhang ZY, Yuan K et al (2013) MiR-133a modulates osteogenic differentiation of vascular smooth muscle cells. Endocrinology 154:3344–3352
Goettsch C, Rauner M, Pacyna N et al (2011) miR-125b regulates calcification of vascular smooth muscle cells. Am J Pathol 179:1594–1600
Mackenzie NC, Staines KA, Zhu D et al (2014) miRNA-221 and miRNA-222 synergistically function to promote vascular calcification. Cell Biochem Funct 32:209–216
Wu T, Zhou H, Hong Y et al (2012) miR-30 family members negatively regulate osteoblast differentiation. J Biol Chem 287:7503–7511
Balderman JA, Lee HY, Mahoney CE et al (2012) Bone morphogenetic protein-2 decreases microRNA-30b and microRNA-30c to promote vascular smooth muscle cell calcification. J Am Heart Assoc 1:e003905
Cui RR, Li SJ, Liu LJ et al (2012) MicroRNA-204 regulates vascular smooth muscle cell calcification in vitro and in vivo. Cardiovasc Res 96:320–329
Thomou T, Mori MA, Dreyfuss JM et al (2017) Adipose-derived circulating miRNAs regulate gene expression in other tissues. Nature 542:450–455
Acknowledgements
This manuscript was supported by a CONACYT grant No. 233493. María de Jesús Luna-Luna is a doctoral student from “Programa de Doctorado en Ciencias Biomédicas de la Universidad Nacional Autónoma de México” and received fellowships from CONACYT, No. 408097 and EXP-AYTE-17345.
Author information
Authors and Affiliations
Corresponding author
Editor information
Editors and Affiliations
Rights and permissions
Copyright information
© 2020 Springer Nature Switzerland AG
About this chapter
Cite this chapter
Luna-Luna, M., Zentella-Dehesa, A., Pérez-Méndez, Ó. (2020). Epicardial Adipose Tissue in the Progression and Calcification of the Coronary Artery Disease. In: Tappia, P.S., Bhullar, S.K., Dhalla, N.S. (eds) Biochemistry of Cardiovascular Dysfunction in Obesity. Advances in Biochemistry in Health and Disease, vol 20. Springer, Cham. https://doi.org/10.1007/978-3-030-47336-5_11
Download citation
DOI: https://doi.org/10.1007/978-3-030-47336-5_11
Published:
Publisher Name: Springer, Cham
Print ISBN: 978-3-030-47335-8
Online ISBN: 978-3-030-47336-5
eBook Packages: Biomedical and Life SciencesBiomedical and Life Sciences (R0)