Villar-Fincheira Paulina, Sanhueza-Olivares Fernanda, Norambuena-Soto Ignacio, Cancino-Arenas Nicole, Hernandez-Vargas Felipe, Troncoso Rodrigo, Gabrielli Luigi, Chiong Mario
Advanced Center for Chronic Diseases & CEMC, Faculty of Chemical and Pharmaceutical Sciences, Universidad de Chile, Santiago, Chile.
Laboratorio de Investigación en Nutrición y Actividad Física (LABINAF), Instituto de Nutrición y Tecnología de los Alimentos, Universidad de Chile, Santiago, Chile.
Front Mol Biosci. 2021 Mar 16;8:641734. doi: 10.3389/fmolb.2021.641734. eCollection 2021.
IL-6 is usually described as a pleiotropic cytokine produced in response to tissue injury or infection. As a pro-inflammatory cytokine, IL-6 activates innate and adaptative immune responses. IL-6 is released in the innate immune response by leukocytes as well as stromal cells upon pattern recognition receptor activation. IL-6 then recruits immune cells and triggers B and T cell response. Dysregulated IL-6 activity is associated with pathologies involving chronic inflammation and autoimmunity, including atherosclerosis. However, IL-6 is also produced and released under beneficial conditions, such as exercise, where IL-6 is associated with the anti-inflammatory and metabolic effects coupled with physical adaptation to intense training. Exercise-associated IL-6 acts on adipose tissue to induce lipogenesis and on arteries to induce adaptative vascular remodeling. These divergent actions could be explained by complex signaling networks. Classical IL-6 signaling involves a membrane-bound IL-6 receptor and glycoprotein 130 (gp130), while trans-signaling relies on a soluble version of IL-6R (sIL-6R) and membrane-bound gp130. Trans-signaling, but not the classical pathway, is regulated by soluble gp130. In this review, we discuss the similarities and differences in IL-6 cytokine and myokine signaling to explain the differential and opposite effects of this protein during inflammation and exercise, with a special focus on the vascular system.
白细胞介素-6(IL-6)通常被描述为一种多效性细胞因子,在组织损伤或感染时产生。作为一种促炎细胞因子,IL-6可激活先天性和适应性免疫反应。在模式识别受体激活后,IL-6在先天性免疫反应中由白细胞以及基质细胞释放。然后,IL-6募集免疫细胞并触发B细胞和T细胞反应。IL-6活性失调与包括动脉粥样硬化在内的涉及慢性炎症和自身免疫的病理状况相关。然而,IL-6也在有益条件下产生和释放,比如运动时,此时IL-6与抗炎和代谢作用以及对高强度训练的身体适应相关。运动相关的IL-6作用于脂肪组织以诱导脂肪生成,作用于动脉以诱导适应性血管重塑。这些不同的作用可以用复杂的信号网络来解释。经典的IL-6信号传导涉及膜结合的IL-6受体和糖蛋白130(gp130),而转信号传导则依赖于可溶性IL-6受体(sIL-6R)和膜结合的gp130。转信号传导而非经典途径受可溶性gp130调节。在这篇综述中,我们讨论IL-6细胞因子和肌动蛋白信号传导的异同,以解释该蛋白在炎症和运动过程中的不同及相反作用,特别关注血管系统。