Radványi Ádám, Röszer Tamás
Department of Pediatrics, Faculty of Medicine, University of Debrecen, H-4032 Debrecen, Hungary.
Int J Mol Sci. 2024 Feb 28;25(5):2810. doi: 10.3390/ijms25052810.
Adipose tissue inflammation is a key factor leading to obesity-associated immune disorders, such as insulin resistance, beta cell loss in the pancreatic islets, meta-inflammation, and autoimmunity. Inhibiting adipose tissue inflammation is considered a straightforward approach to abrogate these diseases. However, recent findings show that certain pro-inflammatory cytokines are essential for the proper differentiation and functioning of adipocytes. Lipolysis is stimulated, and the thermogenic competence of adipocytes is unlocked by interleukin-6 (IL-6), a cytokine that was initially recognized as a key trigger of adipose tissue inflammation. Coherently, signal transducer and activator of transcription 3 (STAT3), which is a signal transducer for IL-6, is necessary for thermogenic adipocyte development. Given the impact of thermogenic adipocytes in increasing energy expenditure and reducing body adiposity, functions of IL-6 in the adipose tissue have gained attention recently. In this review, we show that IL-6 signaling may protect from excess fat accumulation by stimulating thermogenesis in adipocytes.
脂肪组织炎症是导致肥胖相关免疫紊乱的关键因素,如胰岛素抵抗、胰岛β细胞丢失、代谢性炎症和自身免疫。抑制脂肪组织炎症被认为是消除这些疾病的直接方法。然而,最近的研究结果表明,某些促炎细胞因子对于脂肪细胞的正常分化和功能至关重要。脂解作用受到刺激,白细胞介素-6(IL-6)开启了脂肪细胞的产热能力,IL-6最初被认为是脂肪组织炎症的关键触发因素。相应地,作为IL-6信号转导子的信号转导和转录激活因子3(STAT3)对于产热脂肪细胞的发育是必需的。鉴于产热脂肪细胞在增加能量消耗和减少身体脂肪方面的作用,IL-6在脂肪组织中的功能最近受到了关注。在这篇综述中,我们表明IL-6信号传导可能通过刺激脂肪细胞产热来防止过多脂肪堆积。