Local Production of Fatty Acid-Binding Protein 4 in Epicardial/Perivascular Fat and Macrophages Is Linked to Coronary Atherosclerosis

被引:100
作者
Furuhashi, Masato [1 ]
Fuseya, Takahiro [1 ]
Murata, Masaki [2 ]
Hoshina, Kyoko [1 ]
Ishimura, Shutaro [1 ,4 ]
Mita, Tomohiro [1 ]
Watanabe, Yuki [1 ]
Omori, Akina [1 ]
Matsumoto, Megumi [1 ]
Sugaya, Takeshi [5 ,6 ]
Oikawa, Tsuyoshi [6 ]
Nishida, Junichi [1 ]
Kokubu, Nobuaki [1 ]
Tanaka, Marenao [1 ]
Moniwa, Norihito [1 ]
Yoshida, Hideaki [1 ]
Sawada, Norimasa [2 ]
Shimamoto, Kazuaki [3 ]
Miura, Tetsuji [1 ,4 ]
机构
[1] Sapporo Med Univ, Sch Med, Dept Cardiovasc Renal & Metab Med, Sapporo, Hokkaido, Japan
[2] Sapporo Med Univ, Sch Med, Dept Mol & Cellular Pathol, Sapporo, Hokkaido, Japan
[3] Sapporo Med Univ, Chuo Ku, Sapporo, Hokkaido, Japan
[4] Obihiro Kosei Hosp, Dept Cardiovasc Internal Med, Obihiro, Hokkaido, Japan
[5] St Marianna Univ, Sch Med, Dept Hypertens & Nephrol, Miyamae Ku, Kawasaki, Kanagawa, Japan
[6] CIMIC Co Ltd, Bunkyo Ku, Tokyo, Japan
关键词
adipokine; atherosclerosis; coronary stenosis; fatty acid-binding protein 4; macrophage; EPICARDIAL ADIPOSE-TISSUE; INSULIN-RESISTANCE; APOLIPOPROTEIN-E; FABP4; LEVEL; OBESITY; AP2; EXPRESSION; HEART; IDENTIFICATION; ADIPOCYTES;
D O I
10.1161/ATVBAHA.116.307225
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Objective-Fatty acid-binding protein 4 (FABP4) is expressed in adipocytes and macrophages, and elevated circulating FABP4 level is associated with obesity-mediated metabolic phenotype. We systematically investigated roles of FABP4 in the development of coronary artery atherosclerosis. Approach and Results-First, by immunohistochemical analyses, we found that FABP4 was expressed in macrophages within coronary atherosclerotic plaques and epicardial/perivascular fat in autopsy cases and macrophages within thrombi covering ruptured coronary plaques in thrombectomy samples from patients with acute myocardial infarction. Second, we confirmed that FABP4 was secreted from macrophages and adipocytes cultured in vitro. Third, we investigated the effect of exogenous FABP4 on macrophages and human coronary artery-derived smooth muscle cells and endothelial cells in vitro. Treatment of the cells with recombinant FABP4 significantly increased gene expression of inflammatory markers in a dose-dependent manner. Finally, we measured serum FABP4 level in the aortic root (Ao-FABP4) and coronary sinus (CS-FABP4) of 34 patients with suspected or known coronary artery disease. Coronary stenosis score assessed by the modified Gensini score was weakly correlated with CS-FABP4 but was not correlated with Ao-FABP4. A stronger correlation (r=0.59, P<0.01) was observed for the relationship between coronary stenosis score and coronary veno-arterial difference in FABP4 level, (CS-Ao)-FABP4, indicating local production of FABP4 during coronary circulation in the heart. Multivariate analysis indicated that (CS-Ao)-FABP4 was an independent predictor of the severity of coronary stenosis after adjustment of conventional risk factors. Conclusions-FABP4 locally produced by epicardial/perivascular fat and macrophages in vascular plaques contributes to the development of coronary atherosclerosis.
引用
收藏
页码:825 / 834
页数:10
相关论文
共 49 条
  • [1] Expression of fatty acid-binding protein 4/aP2 is correlated with plaque instability in carotid atherosclerosis
    Agardh, H. E.
    Folkersen, L.
    Ekstrand, J.
    Marcus, D.
    Swedenborg, J.
    Hedin, U.
    Gabrielsen, A.
    Paulsson-Berne, G.
    [J]. JOURNAL OF INTERNAL MEDICINE, 2011, 269 (02) : 200 - 210
  • [2] Perivascular adipose tissue from human systemic and coronary vessels: the emergence of a new pharmacotherapeutic target
    Aghamohammadzadeh, Reza
    Withers, Sarah
    Lynch, Fiona
    Greenstein, Adam
    Malik, R.
    Heagerty, Anthony
    [J]. BRITISH JOURNAL OF PHARMACOLOGY, 2012, 165 (03) : 670 - 682
  • [3] Fatty acid-binding protein 4 impairs the insulin-dependent nitric oxide pathway in vascular endothelial cells
    Aragones, Gemma
    Saavedra, Paula
    Heras, Mercedes
    Cabre, Anna
    Girona, Josefa
    Masana, Lluis
    [J]. CARDIOVASCULAR DIABETOLOGY, 2012, 11
  • [4] Combined adipocyte-macrophage fatty acid-binding protein deficiency improves metabolism, atherosclerosis, and survival in apolipoprotein E-deficient mice
    Boord, JB
    Maeda, K
    Makowski, L
    Babaev, VR
    Fazio, S
    Linton, MF
    Hotamisligil, GS
    [J]. CIRCULATION, 2004, 110 (11) : 1492 - 1498
  • [5] Adipocyte Lipid Chaperone aP2 Is a Secreted Adipokine Regulating Hepatic Glucose Production
    Cao, Haiming
    Sekiya, Motohiro
    Ertunc, Meric Erikci
    Burak, M. Furkan
    Mayers, Jared R.
    White, Ariel
    Inouye, Karen
    Rickey, Lisa M.
    Ercal, Baris C.
    Furuhashi, Masato
    Tuncman, Guerol
    Hotamisligil, Goekhan S.
    [J]. CELL METABOLISM, 2013, 17 (05) : 768 - 778
  • [6] Elevated Circulating Adipocyte-Fatty Acid Binding Protein Levels Predict Incident Cardiovascular Events in a Community-Based Cohort: A 12-Year Prospective Study
    Chow, Wing Sun
    Tso, Annette Wai Kwan
    Xu, Aimin
    Yuen, Michele Mae Ann
    Fong, Carol Ho Yi
    Lam, Tai Hing
    Lo, Su Vui
    Tse, Hung Fat
    Woo, Yu Cho
    Yeung, Chun Yip
    Cheung, Bernard Man Yung
    Lam, Karen Siu Ling
    [J]. JOURNAL OF THE AMERICAN HEART ASSOCIATION, 2013, 2 (01): : e004176
  • [7] Association of increased plasma adipocyte fatty acid-binding protein with coronary artery disease in non-elderly men
    Doi, Masayuki
    Miyoshi, Toru
    Hirohata, Satoshi
    Nakamura, Kazufumi
    Usui, Shinichi
    Takeda, Ko
    Iwamoto, Mutsumi
    Kusachi, Shozo
    Kusano, Kengo
    Ito, Hiroshi
    [J]. CARDIOVASCULAR DIABETOLOGY, 2011, 10
  • [8] Fu YC, 2000, J LIPID RES, V41, P2017
  • [9] Fatty acid-binding proteins: role in metabolic diseases and potential as drug targets
    Furuhashi, Masato
    Hotamisligil, Goekhan S.
    [J]. NATURE REVIEWS DRUG DISCOVERY, 2008, 7 (06) : 489 - 503
  • [10] Adipocyte/macrophage fatty acid-binding proteins contribute to metabolic deterioration through actions in both macrophages and adipocytes in mice
    Furuhashi, Masato
    Fucho, Raquel
    Gorgun, Cem Z.
    Tuncman, Guerol
    Cao, Haiming
    Hotamisligil, Goekhan S.
    [J]. JOURNAL OF CLINICAL INVESTIGATION, 2008, 118 (07) : 2640 - 2650