Taxerås Siri D, Galán María, Campderros Laura, Piquer-Garcia Irene, Pellitero Silvia, Martínez Eva, Puig Rocío, Lucena Icíar, Tarascó Jordi, Moreno Pau, Balibrea José, Bel Joan, Murillo Marta, Martínez María, Ramon-Krauel Marta, Puig-Domingo Manel, Villarroya Francesc, Lerin Carles, Sánchez-Infantes David
Department of Endocrinology and Nutrition Germans Trias i Pujol Research Institute Barcelona Spain.
Institut de Recerca del Hospital de la Santa Creu i Sant Pau-Programa ICCC Barcelona Spain.
Obes Sci Pract. 2019 Dec 2;6(1):99-106. doi: 10.1002/osp4.381. eCollection 2020 Feb.
S100A4 has been recently identified as an adipokine associated with insulin resistance (IR) in adult subjects with obesity. However, no data about its levels in children with obesity and only a few approaches regarding its potential mechanism of action have been reported. To obtain a deeper understanding of the role of S100A4 in obesity, (a) S100A4 levels were measured in prepubertal children and adult subjects with and without obesity and studied the relationship with IR and (b) the effects of S100A4 in cultured human adipocytes and vascular smooth muscle cells (VSMCs) were determined.
Sixty-five children (50 with obesity, age 9.0 ±1.1 years and 15 normal weight, age 8.4 ±0.8 years) and fifty-nine adults (43 with severe obesity, age 46 ±11 years and 16 normal weight, age 45 ±9 years) were included. Blood from children and adults and adipose tissue samples from adults were obtained and analysed. Human adipocytes and VSMC were incubated with S100A4 to evaluate their response to this adipokine.
Circulating S100A4 levels were increased in both children ( = .002) and adults ( < .001) with obesity compared with their normal-weight controls. In subjects with obesity, S100A4 levels were associated with homeostatic model assessment-insulin resistance (HOMA-IR) in adults ( = .42, = .008) but not in children ( = .12, = .356). Human adipocytes were not sensitive to S100A4, while incubation with this adipokine significantly reduced inflammatory markers in VSMC.
Our human data demonstrate that higher S100A4 levels are a marker of IR in adults with obesity but not in prepubertal children. Furthermore, the in vitro results suggest that S100A4 might exert an anti-inflammatory effect. Further studies will be necessary to determine whether S100A4 can be a therapeutic target for obesity.
S100A4最近被确定为一种与肥胖成年受试者胰岛素抵抗(IR)相关的脂肪因子。然而,关于肥胖儿童中其水平的数据尚未见报道,且关于其潜在作用机制的研究方法也很少。为了更深入了解S100A4在肥胖中的作用,(a)测量了青春期前肥胖和非肥胖儿童及成年受试者的S100A4水平,并研究了其与IR的关系;(b)确定了S100A4对培养的人脂肪细胞和血管平滑肌细胞(VSMC)的影响。
纳入65名儿童(50名肥胖儿童,年龄9.0±1.1岁,15名正常体重儿童,年龄8.4±0.8岁)和59名成年人(43名重度肥胖成年人,年龄46±11岁,16名正常体重成年人,年龄45±9岁)。采集儿童和成年人的血液以及成年人的脂肪组织样本并进行分析。将人脂肪细胞和VSMC与S100A4共同孵育,以评估它们对这种脂肪因子的反应。
与正常体重对照组相比,肥胖儿童(P = 0.002)和成年人(P < 0.001)的循环S100A4水平均升高。在肥胖受试者中,S100A4水平与成年人的稳态模型评估胰岛素抵抗(HOMA-IR)相关(r = 0.42,P = 0.008),但与儿童无关(r = 0.12,P = 0.356)。人脂肪细胞对S100A4不敏感,而用这种脂肪因子孵育可显著降低VSMC中的炎症标志物。
我们的人体数据表明,较高的S100A4水平是肥胖成年人IR的标志物,但不是青春期前儿童的标志物。此外,体外实验结果表明,S100A4可能具有抗炎作用。需要进一步研究以确定S100A4是否可成为肥胖的治疗靶点。