Department of Pediatrics, Division of Immunology, Faculty of Medicine and Heath Sciences, Université de Sherbrooke, Sherbrooke, QC, Canada.
Centre de Recherche, Centre Hospitalier Universitaire de Sherbrooke (CRCHUS), Sherbrooke, QC, Canada.
EBioMedicine. 2018 Apr;30:237-247. doi: 10.1016/j.ebiom.2018.03.004. Epub 2018 Mar 8.
Population studies have linked insulin resistance to systemic low-grade chronic inflammation and have reported elevated levels of inflammatory cytokines such as TNFα, IL-1β and IL-6, individually or in certain combinations, in adipose tissues or in the serum. We undertook this comprehensive study to simultaneously evaluate the expression of several pro-inflammatory and anti-inflammatory cytokines in serum and in the visceral and subcutaneous adipose tissues from obese patients undergoing bariatric surgery. We observed that several inflammatory cytokines implicated in obesity-associated inflammation showed no significant difference in protein or gene expression between obese patients with or without diabetes and control groups. IL1B gene expression was significantly elevated in the visceral adipose tissues of obese patients, but did not correlate with their diabetes status. Despite the significant increase in IL1B expression in the obese group, a significant proportion of obese patients did not express TNFA, IL1B or IL6 in visceral adipose tissues. Certain inflammatory cytokines showed correlation with the chemokine CCL2 and VEGF-A in visceral adipose tissues. Our findings suggest that the inflammatory cytokine profile in metabolic syndrome is more complex than what is currently perceived and that chronic inflammation in obese patients likely results from incremental contribution from different cytokines and possibly other inflammatory mediators from within and outside the adipose tissues. It is possible that this obesity associated chronic inflammation is not predicted by a single mediator, but rather includes a large spectrum of possible profiles.
人群研究将胰岛素抵抗与全身低度慢性炎症联系起来,并报告了脂肪组织或血清中炎症细胞因子(如 TNFα、IL-1β 和 IL-6)水平升高,这些因子单独或组合存在。我们进行了这项综合研究,以同时评估接受减肥手术的肥胖患者的血清以及内脏和皮下脂肪组织中几种促炎和抗炎细胞因子的表达。我们观察到,几种与肥胖相关炎症相关的炎症细胞因子在有或没有糖尿病的肥胖患者和对照组之间的蛋白或基因表达没有显著差异。IL1B 基因在肥胖患者的内脏脂肪组织中表达显著升高,但与他们的糖尿病状态无关。尽管肥胖组的 IL1B 表达显著增加,但相当一部分肥胖患者的内脏脂肪组织中不表达 TNFA、IL1B 或 IL6。某些炎症细胞因子与内脏脂肪组织中的趋化因子 CCL2 和 VEGF-A 相关。我们的研究结果表明,代谢综合征中的炎症细胞因子谱比目前所认为的更为复杂,肥胖患者的慢性炎症可能是由不同细胞因子和可能来自脂肪组织内外的其他炎症介质的增量贡献所致。肥胖相关的慢性炎症可能不是由单一介质预测的,而是包括可能的多种可能的情况。