Visfatin, an adipocytokine with proinflammatory and immunomodulating properties

被引:775
作者
Moschen, Alexander R.
Kaser, Arthur
Enrich, Barbara
Mosheimer, Birgit
Theurl, Milan
Niederegger, Harald
Tilg, Herbert [1 ]
机构
[1] Innsbruck Med Univ, Dept Med, Clin Div Gastroenterol & Hepatol, Christian Doppler Res Lab Gut Inflammat, A-6020 Innsbruck, Austria
[2] Innsbruck Med Univ, Dept Med, Clin Div Gen Internal Med, A-6020 Innsbruck, Austria
[3] Innsbruck Med Univ, Div Expt Pathophysiol & Immunol, Innsbruck Bioctr, A-6020 Innsbruck, Austria
关键词
D O I
10.4049/jimmunol.178.3.1748
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Adipocytokines are mainly adipocyte-derived cytokines regulating metabolism and as such are key regulators of insulin resistance. Some adipocytokines such as adiponectin and leptin affect immune and inflammatory functions. Visfatin (pre-B cell colony-enhancing factor) has recently been identified as a new adipocytokine affecting insulin resistance by binding to the insulin receptor. In this study, we show that recombinant visfatin activates human leukocytes and induces cytokine production. In CD14(+) monocytes, visfatin induces the production of IL-1 beta, TNF-alpha, and especially IL-6. Moreover, it increases the surface expression of costimulatory molecules CD54, CD40, and CD80. Visfatin-stimulated monocytes show augmented FITC-dextran uptake and an enhanced capacity to induce alloproliferative responses in human lymphocytes. Visfatin-induced effects involve p38 as well as MEK1 pathways as determined by inhibition with MAPK inhibitors and we observed activation of NF-kappa B. In vivo, visfatin induces circulating IL-6 in BALB/c mice. In patients with inflammatory bowel disease, plasma levels of visfatin are elevated and its mRNA expression is significantly increased in colonic tissue of Crohn's and ulcerative colitis patients compared with healthy controls. Macrophages, dendritic cells, and colonic epithelial cells might be additional sources of visfatin as determined by confocal microscopy. Visfatin can be considered anew proinflammatory adipocytokine.
引用
收藏
页码:1748 / 1758
页数:11
相关论文
共 64 条
[1]   The survival kinases Akt and Pim as potential pharmacological targets [J].
Amaravadi, R ;
Thompson, CB .
JOURNAL OF CLINICAL INVESTIGATION, 2005, 115 (10) :2618-2624
[2]   Blockade of interleukin 6 trans signaling suppresses T-cell resistance against apoptosis in chronic intestinal inflammation:: Evidence in Crohn disease and experimental colitis in vivo [J].
Atreya, R ;
Mudter, J ;
Finotto, S ;
Müllberg, J ;
Jostock, T ;
Wirtz, S ;
Schütz, M ;
Bartsch, B ;
Holtmann, M ;
Becker, C ;
Strand, D ;
Czaja, J ;
Schlaak, JF ;
Lehr, HA ;
Autschbach, F ;
Schürmann, G ;
Nishimoto, N ;
Yoshizaki, K ;
Ito, H ;
Kishimoto, T ;
Galle, PR ;
Rose-John, S ;
Neurath, MF .
NATURE MEDICINE, 2000, 6 (05) :583-588
[3]   Plasma visfatin concentrations and fat depot-specific mRNA expression in humans [J].
Berndt, J ;
Klöting, N ;
Kralisch, S ;
Kovacs, P ;
Fasshauer, M ;
Schön, MR ;
Stumvoll, M ;
Blüher, M .
DIABETES, 2005, 54 (10) :2911-2916
[4]  
BEST WR, 1976, GASTROENTEROLOGY, V70, P439
[5]  
Boyum A, 1968, Scand J Clin Lab Invest Suppl, V97, P7
[6]   Elevated plasma level of visfatin/pre-B cell colony-enhancing factor in patients with type 2 diabetes mellitus [J].
Chen, MP ;
Chung, FM ;
Chang, DM ;
Tsai, JCR ;
Huang, HF ;
Shin, SJ ;
Lee, YJ .
JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 2006, 91 (01) :295-299
[7]   Liver failure and defective hepatocyte regeneration in interleukin-6-deficient mice [J].
Cressman, DE ;
Greenbaum, LE ;
DeAngelis, RA ;
Ciliberto, G ;
Furth, EE ;
Poli, V ;
Taub, R .
SCIENCE, 1996, 274 (5291) :1379-1383
[8]   Biologic basis for interleukin-1 in disease [J].
Dinarello, CA .
BLOOD, 1996, 87 (06) :2095-2147
[9]   Chemokines: Key players in innate and adaptive immunity [J].
Esche, C ;
Stellato, C ;
Beck, LA .
JOURNAL OF INVESTIGATIVE DERMATOLOGY, 2005, 125 (04) :615-628
[10]   Comparison of the release of adipokines by adipose tissue, adipose tissue matrix, and Adipocytes from visceral and subcutaneous abdominal adipose tissues of obese humans [J].
Fain, JN ;
Madan, AK ;
Hiler, ML ;
Cheema, P ;
Bahouth, SW .
ENDOCRINOLOGY, 2004, 145 (05) :2273-2282