Immunometabolism, Department of Nutrition, Nursing School, Universidade Federal de Minas Gerais, Belo Horizonte, Minas Gerais, Brazil.
Faculty of Nutrition, Universidade Federal de Alfenas, Alfenas, Brazil.
Int J Obes (Lond). 2024 Jul;48(7):964-972. doi: 10.1038/s41366-024-01507-5. Epub 2024 Mar 8.
BACKGROUND/OBJECTIVES: Proinflammatory cytokines are increased in obese adipose tissue, including inflammasome key masters. Conversely, IL-18 protects against obesity and metabolic dysfunction. We focused on the IL-18 effect in controlling adipose tissue remodeling and metabolism.
MATERIALS/SUBJECTS AND METHODS: We used C57BL/6 wild-type (WT) and interleukine-18 deficient (IL-18) male mice fed a chow diet and samples from bariatric surgery patients.
IL-18 mice showed increased adiposity and proinflammatory cytokine levels in adipose tissue, leading to glucose intolerance. IL-18 was widely secreted by stromal vascular fraction but not adipocytes from mice's fatty tissue. Chimeric model experiments indicated that IL-18 controls adipose tissue expansion through its presence in tissues other than bone marrow. However, IL-18 maintains glucose homeostasis when present in bone marrow cells. In humans with obesity, IL-18 expression in omental tissue was not correlated with BMI or body fat mass but negatively correlated with IRS1, GLUT-4, adiponectin, and PPARy expression. Also, the IL-18RAP receptor was negatively correlated with IL-18 expression.
IL-18 signaling may control adipose tissue expansion and glucose metabolism, as its absence leads to spontaneous obesity and glucose intolerance in mice. We suggest that resistance to IL-18 signaling may be linked with worse glucose metabolism in humans with obesity.
背景/目的:促炎细胞因子在肥胖的脂肪组织中增加,包括炎性小体的关键调节因子。相反,IL-18 可预防肥胖和代谢功能障碍。我们专注于 IL-18 对控制脂肪组织重塑和代谢的作用。
材料/对象和方法:我们使用 C57BL/6 野生型(WT)和白细胞介素-18 缺乏(IL-18)雄性小鼠,用普通饮食喂养,并使用来自减肥手术患者的样本。
IL-18 小鼠表现出脂肪组织中脂肪增多和促炎细胞因子水平升高,导致葡萄糖不耐受。IL-18 由基质血管部分广泛分泌,但不是来自小鼠脂肪组织的脂肪细胞。嵌合模型实验表明,IL-18 通过存在于骨髓以外的组织控制脂肪组织的扩张。但是,当存在于骨髓细胞中时,IL-18 维持葡萄糖的体内平衡。在肥胖的人类中,网膜组织中的 IL-18 表达与 BMI 或体脂肪量无关,但与 IRS1、GLUT-4、脂联素和 PPARγ的表达呈负相关。此外,IL-18RAP 受体与 IL-18 的表达呈负相关。
IL-18 信号可能控制脂肪组织的扩张和葡萄糖代谢,因为其缺失会导致小鼠自发性肥胖和葡萄糖不耐受。我们认为,肥胖人群中对 IL-18 信号的抗性可能与葡萄糖代谢恶化有关。