Correlation of Peroxisome Proliferator-Activated Receptor-γ (PPAR-γ) and Retinoid X Receptor-α (RXR-α) expression with clinical risk factors in patients with advanced carotid atherosclerosis

被引:27
|
作者
Giaginis, Constantinos [2 ]
Klonaris, Christos [3 ]
Katsargyris, Athanasios [3 ]
Kouraklis, Gregorios [2 ]
Spiliopoulou, Chara
Theocharis, Stamatios [1 ]
机构
[1] Univ Athens, Sch Med, Dept Forens Med & Toxicol, GR-11527 Athens, Greece
[2] Univ Athens, Sch Med, Dept Propedeut Surg 2, GR-11527 Athens, Greece
[3] Univ Athens, Sch Med, Dept Surg 1, GR-11527 Athens, Greece
来源
MEDICAL SCIENCE MONITOR | 2011年 / 17卷 / 07期
关键词
carotid atherosclerosis; immunohistochemistry; macrophages; PPAR-gamma; RXR-alpha; smooth muscle cells; E-KNOCKOUT MICE; INHIBITS ATHEROSCLEROSIS; THERAPEUTIC TARGET; GENE-EXPRESSION; LIGANDS; DIFFERENTIATION; INFLAMMATION; STENOSIS; PATHWAY; ENDARTERECTOMY;
D O I
10.12659/MSM.881849
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
Background: Peroxisome proliferator-activated receptor-gamma (PPAR-gamma) and its nuclear partners, the Retinoid X Receptors (RXRs), have been recognized as crucial players in the pathogenesis of atherosclerosis. The present study aimed to assess the clinical significance of PPAR-gamma and RXR-alpha expression in different cellular populations localized within advanced carotid atherosclerosis lesions. Material/Methods: PPAR-gamma and RXR-alpha expression was assessed by immunohistochemistry in 134 carotid atherosclerotic plaques obtained from an equal number of patients that underwent endarterectomy procedure for vascular repair, and was correlated with patients' medical history, risk factors and medication intake. Results: Increased incidence of low PPAR-g expression in both macrophages and smooth muscle cells was noted in patients presenting coronary artery disease (p=0.032 and p=0.046, respectively). PPAR-gamma expression in smooth muscle cells was borderline down-regulated in symptomatic compared to asymptomatic patients (p=0.061), reaching statistical significance when analyzing groups of patients with specific cerebrovascular events; amaurosis fugax (p=0.008), amaurosis fugax/stroke (p=0.020) or amaurosis fugax/transient ischemic attack patients (p=0.028) compared to asymptomatic patients. Low RXR-alpha expression in macrophages was more frequently observed in hypertensive (p=0.048) and hyperlipidemic patients (p=0.049). Increased incidence of low RXR-alpha expression in smooth muscle cells was also noted in patients presenting advanced carotid stenosis grade (p=0.015). Conclusions: PPAR-gamma and RXR-alpha expression down-regulation in macrophages and smooth muscle cells was associated with a more pronounced disease progression in patients with advanced carotid atherosclerotic lesions.
引用
收藏
页码:CR381 / CR391
页数:11
相关论文
共 50 条
  • [31] Expression of peroxisome proliferator-activated receptor gamma (PPAR-γ) in canine nasal carcinomas
    Paciello, O.
    Borzacchiello, G.
    Varricchio, E.
    Papparella, S.
    JOURNAL OF VETERINARY MEDICINE SERIES A-PHYSIOLOGY PATHOLOGY CLINICAL MEDICINE, 2007, 54 (08): : 406 - 410
  • [32] PD-1 expression affects cytokine production by ILC2 and is influenced by peroxisome proliferator-activated receptor-γ
    Batyrova, Banu
    Luwaert, Fien
    Maravelia, Panagiota
    Miyabayashi, Yuria
    Vashist, Neha
    Stark, Julian M.
    Soori, Sara Y.
    Tibbitt, Christopher A.
    Riese, Peggy
    Coquet, Jonathan M.
    Chambers, Benedict J.
    IMMUNITY INFLAMMATION AND DISEASE, 2020, 8 (01) : 8 - 23
  • [33] Hepatic Steatosis with Relation to Increased Expression of Peroxisome Proliferator-Activated Receptor-γ in Insulin Resistant Mice
    Satoh, Hikaru
    Ide, Naohito
    Kagawa, Yoshiyuki
    Maeda, Toshio
    BIOLOGICAL & PHARMACEUTICAL BULLETIN, 2013, 36 (04) : 616 - 623
  • [34] Bisphenol A is a carcinogen that induces lipid accumulation, peroxisome proliferator-activated receptor-γ expression and liver disease
    Ismael, Layla Qasim
    Abdulhameed, Ahmed Rashid
    Keong, Yong Yoke
    Abdullah, Muhammad Nazrul Hakim
    Bahari, Hasnah
    Jie, Tan Jun
    Yin, Khoo Boon
    EXPERIMENTAL AND THERAPEUTIC MEDICINE, 2022, 24 (06)
  • [35] Macrophage expression of peroxisome proliferator-activated receptor-α reduces atherosclerosis in low-density lipoprotein receptor-deficient mice
    Babaev, Vladimir R.
    Ishiguro, Hiroyuki
    Ding, Lei
    Yancey, Patricia G.
    Dove, Dwayne E.
    Kovacs, William J.
    Semenkovich, Clay F.
    Fazio, Sergio
    Linton, MacRae F.
    CIRCULATION, 2007, 116 (12) : 1404 - 1412
  • [36] Tobacco smoke affects expression of peroxisome proliferator-activated receptor-γ in monocyte/macrophages of patients with coronary heart disease
    Amoruso, A.
    Gunella, G.
    Rondano, E.
    Bardelli, C.
    Fresu, L. G.
    Ferrero, V.
    Ribichini, F.
    Vassanelli, C.
    Brunelleschi, S.
    BRITISH JOURNAL OF PHARMACOLOGY, 2009, 158 (05) : 1276 - 1284
  • [37] Evidence for differential effects of glucose and cycloheximide on mRNA levels of peroxisome proliferator-activated receptor- (PPAR-) machinery members: Superinduction of PPAR-γ1 and -γ2 mRNAs
    Rypka, Miroslav
    Vesely, Jaroslav
    ACTA BIOCHIMICA POLONICA, 2010, 57 (02) : 209 - 215
  • [38] Activation of peroxisome proliferator-activated receptor-γ (PPAR-γ) by atorvastatin is mediated by 15-deoxy-delta-12,14-PGJ2
    Ye, Yumei
    Nishi, Shawn P.
    Manickavasagam, Saraswathy
    Lin, Yu
    Huang, Ming-He
    Perez-Polo, J. Regino
    Uretskya, Barry F.
    Birnbaum, Yochai
    PROSTAGLANDINS & OTHER LIPID MEDIATORS, 2007, 84 (1-2) : 43 - 53
  • [39] Relationship between peroxisome proliferator-activated receptor-γ mRNA expression and intracranial aneurysm rupture
    Zhang, Xiong
    Kang, Yan-Xun
    Kong, Wei
    Zhang, Ya-Lan
    Ju, Tao
    EUROPEAN JOURNAL OF INFLAMMATION, 2021, 19
  • [40] The peroxisome proliferator-activated receptor-α (PPAR-α) agonist, AVE8134, attenuates the progression of heart failure and increases survival in rats
    Linz, Wolfgang
    Wohlfart, Paulus
    Baader, Manuel
    Breitschopf, Kristin
    Falk, Eugen
    Schaefer, Hans-Ludwig
    Gerl, Martin
    Kramer, Werner
    Ruetten, Hartmut
    ACTA PHARMACOLOGICA SINICA, 2009, 30 (07) : 935 - 946