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IL-18 在脂肪组织重塑和代谢功能障碍中的作用。

Role of IL-18 in adipose tissue remodeling and metabolic dysfunction.

机构信息

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.

出版信息

Int J Obes (Lond). 2024 Jul;48(7):964-972. doi: 10.1038/s41366-024-01507-5. Epub 2024 Mar 8.

DOI:10.1038/s41366-024-01507-5
PMID:38459259
Abstract

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.

RESULTS

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.

CONCLUSIONS

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.

摘要

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。

结果

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。

结论

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。

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