Roles of IL-6-gp130 Signaling in Vascular Inflammation

被引:121
作者
Hou, Tieying
Tieu, Brian C.
Ray, Sutapa
Recinos, Adrian, III
Cui, Ruwen
Tilton, Ronald G.
Brasier, Allan R.
机构
[1] Univ Texas Med Branch, Dept Biochem & Mol Biol, Galveston, TX 77555 USA
[2] Univ Texas Med Branch, Dept Internal Med, Galveston, TX 77555 USA
[3] Univ Texas Med Branch, Sealy Ctr Mol Med, Galveston, TX 77555 USA
关键词
IL-6; gp-130; angiotensin II; STAT3; vascular inflammation;
D O I
10.2174/157340308785160570
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Interleukin-6 (IL-6) is a well-established, independent indicator of multiple distinct types of cardiovascular disease and all-cause mortality. In this review, we present current understanding of the multiple roles that IL-6 and its signaling pathways through glycoprotein 130 (gp130) play in cardiovascular homeostasis. IL-6 is highly inducible in vascular tissues through the actions of the angiotensin II (Ang II) peptide, where it acts in a paracrine manner to signal through two distinct mechanisms, the first being a classic membrane receptor initiated pathway and the second, a trans-signaling pathway, being able to induce responses even in tissues lacking the IL-6 receptor. Recent advances and new concepts in how its intracellular signaling pathways operate via the Janus kinase (JAK)-Signal Transducer and Activator of Transcription (STAT) are described. IL-6 has diverse actions in multiple cell types of cardiovascular importance, including endothelial cells, monocytes, platelets, hepatocytes and adipocytes. We discuss central roles of IL-6 in endothelial dysfunction, cellular inflammation by affecting monocyte activation/differentiation, cellular cytoprotective functions from reactive oxygen species (ROS) stress, modulation of pro-coagulant state, myocardial growth control, and its implications in metabolic control and insulin resistance. These multiple actions indicate that IL-6 is not merely a passive biomarker, but actively modulates adaptive and pathological responses to cardiovascular stress.
引用
收藏
页码:179 / 192
页数:14
相关论文
共 180 条
  • [31] Relationship of interleukin-6 and C-reactive protein to the prothrombotic state in chronic atrial fibrillation
    Conway, DSG
    Buggins, P
    Hughes, E
    Lip, GYH
    [J]. JOURNAL OF THE AMERICAN COLLEGE OF CARDIOLOGY, 2004, 43 (11) : 2075 - 2082
  • [32] Liver failure and defective hepatocyte regeneration in interleukin-6-deficient mice
    Cressman, DE
    Greenbaum, LE
    DeAngelis, RA
    Ciliberto, G
    Furth, EE
    Poli, V
    Taub, R
    [J]. SCIENCE, 1996, 274 (5291) : 1379 - 1383
  • [33] CRESSMAN DE, 1995, HEPATOLOGY, V21, P1443, DOI 10.1016/0270-9139(95)90068-3
  • [34] RhoA mediates angiotensin II-induced phospho-Ser536 nuclear factor κB/Re1A subunit exchange on the interleukin-6 promoter in VSMCs
    Cui, Ruwen
    Tieu, Brian
    Recinos, Adrian
    Tilton, Ronald G.
    Brasier, Allan R.
    [J]. CIRCULATION RESEARCH, 2006, 99 (07) : 723 - 730
  • [35] DAHLBACK B, 1991, THROMB HAEMOSTASIS, V66, P49
  • [36] THE HUMAN BETA-FIBRINOGEN PROMOTER CONTAINS A HEPATOCYTE NUCLEAR FACTOR 1-DEPENDENT INTERLEUKIN-6-RESPONSIVE ELEMENT
    DALMON, J
    LAURENT, M
    COURTOIS, G
    [J]. MOLECULAR AND CELLULAR BIOLOGY, 1993, 13 (02) : 1183 - 1193
  • [37] INTERLEUKIN-6-DEFICIENT MICE ARE HIGHLY SUSCEPTIBLE TO LISTERIA-MONOCYTOGENES INFECTION - CORRELATION WITH INEFFICIENT NEUTROPHILIA
    DALRYMPLE, SA
    LUCIAN, LA
    SLATTERY, R
    MCNEIL, T
    AUD, DM
    FUCHINO, S
    LEE, F
    MURRAY, R
    [J]. INFECTION AND IMMUNITY, 1995, 63 (06) : 2262 - 2268
  • [38] Angiotensin II promotes atherosclerotic lesions and aneurysms in apolipoprotein E-deficient mice
    Daugherty, A
    Manning, MW
    Cassis, LA
    [J]. JOURNAL OF CLINICAL INVESTIGATION, 2000, 105 (11) : 1605 - 1612
  • [39] Critical role for CuZn-superoxide dismutase in preventing angiotensin II-induced endothelial dysfunction
    Didion, SP
    Kinzenbaw, DA
    Faraci, FM
    [J]. HYPERTENSION, 2005, 46 (05) : 1147 - 1153
  • [40] Interleukin-6 and mevastatin regulate plasminogen activator inhibitor-1 through CCAAT/enhancer-binding protein-δ
    Dong, J
    Fujii, S
    Li, HM
    Nakabayashi, H
    Sakai, M
    Nishi, S
    Goto, D
    Furumoto, T
    Imagawa, S
    Zaman, TAKM
    Kitabatake, A
    [J]. ARTERIOSCLEROSIS THROMBOSIS AND VASCULAR BIOLOGY, 2005, 25 (05) : 1078 - 1084