Tacke Christopher, Aleksandrova Krasimira, Rehfeldt Miriam, Murahovschi Veronica, Markova Mariya, Kemper Margrit, Hornemann Silke, Kaiser Ulrike, Honig Caroline, Gerbracht Christiana, Kabisch Stefan, Hörbelt Tina, Ouwens D Margriet, Weickert Martin O, Boeing Heiner, Pfeiffer Andreas F H, Pivovarova Olga, Rudovich Natalia
Department of Endocrinology, Diabetes and Nutrition, Campus Benjamin Franklin, Charité University Medicine, Berlin, Germany.
Department of Clinical Nutrition, German Institute of Human Nutrition Potsdam, Nuthetal, Germany.
J Cell Commun Signal. 2018 Sep;12(3):539-548. doi: 10.1007/s12079-017-0427-1. Epub 2017 Nov 11.
WNT1 inducible signaling pathway protein 1 (WISP-1/CCN4) is a novel adipokine, which is upregulated in obesity, and induces a pro-inflammatory response in macrophages in-vitro. Preclinical observations suggested WISP-1/CCN4 as a potential candidate for novel obesity therapy targeting adipose tissue inflammation. Whether circulating levels of WISP-1/CCN4 in humans are altered in obesity and/or type 2 diabetes (T2DM) and in the postprandial state, however, is unknown. This study assessed circulating WISP-1/CCN4 levels in a) paired liquid meal tests and hyperinsulinemic- euglycemic clamps (cohort I, n = 26), b) healthy individuals (cohort II, n = 207) and c) individuals with different stages of obesity and glucose tolerance (cohort III, n = 253). Circulating plasma and serum WISP-1/CCN4 concentrations were measured using a commercially available ELISA. WISP-1/CCN4 levels were not influenced by changes in insulin and/or glucose during the tests. In healthy individuals, WISP-1/CCN4 was detectable in 13% of plasma samples with the intraclass correlation coefficient of 0.93 (95% CI: 0.84-0.96) and in 58.1% of the serum samples in cohort III. Circulating WISP-1/CCN4 positively correlated with body mass index, body fat percentage, leptin and triglyceride levels, hip circumference and fatty liver index. No differences in WISP-1/CCN4 levels between individuals with normal glucose tolerance, impaired glucose tolerance and T2DM were found. The circulating concentrations of WISP-1/CCN4 showed no acute regulation in postprandial state and correlated with anthropometrical obesity markers and lipid profiles. In healthy individuals, WISP-1/CCN4 levels are more often below the detection limit. Thus, serum WISP-1/CCN4 levels may be used as a suitable biomarker of obesity.
WNT1诱导信号通路蛋白1(WISP-1/CCN4)是一种新型脂肪因子,在肥胖状态下上调,并在体外诱导巨噬细胞产生促炎反应。临床前观察表明,WISP-1/CCN4是针对脂肪组织炎症的新型肥胖治疗的潜在候选物。然而,尚不清楚肥胖和/或2型糖尿病(T2DM)患者以及餐后状态下人类循环中WISP-1/CCN4水平是否会发生变化。本研究评估了以下人群的循环WISP-1/CCN4水平:a)配对液体餐试验和高胰岛素-正常血糖钳夹试验(队列I,n = 26);b)健康个体(队列II,n = 207);c)不同肥胖和糖耐量阶段的个体(队列III,n = 253)。使用市售酶联免疫吸附测定法(ELISA)测量循环血浆和血清中WISP-1/CCN4的浓度。试验期间,WISP-1/CCN4水平不受胰岛素和/或葡萄糖变化的影响。在健康个体中,队列III中13%的血浆样本可检测到WISP-1/CCN4,组内相关系数为0.93(95%CI:0.84-0.96),血清样本中这一比例为58.1%。循环WISP-1/CCN4与体重指数、体脂百分比、瘦素和甘油三酯水平、臀围和脂肪肝指数呈正相关。在糖耐量正常、糖耐量受损和T2DM个体之间,未发现WISP-1/CCN4水平存在差异。WISP-1/CCN4的循环浓度在餐后状态下无急性调节,且与人体测量肥胖标志物和血脂谱相关。在健康个体中,WISP-1/CCN4水平更常低于检测限。因此,血清WISP-1/CCN4水平可作为肥胖的合适生物标志物。