Diverse Cytokines Secreted by Adipocyte in Linking Cardio-Metabolic Disorder and SLE.

IF 3.3 Q2 BIOCHEMISTRY & MOLECULAR BIOLOGY Frontiers in bioscience (Landmark edition) Pub Date : 2024-10-31 DOI:10.31083/j.fbl2911373
Min Lai, Kai Lin, Xiaofang Chen, Ye Cheng
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Abstract

Systemic lupus erythematosus (SLE) is a multi-factorial autoimmune-mediated disease with hyper-stimulation of immune cells especially the T lymphocytes. By this method, it might facilitate the systematic damages in multiple tissues and organs. Otherwise, SLE is also correlated with diverse cardio-metabolic comorbidities, including dyslipidemia, insulin resistance, and hypertension. It is worth-noting that the risk of cardio-metabolic disorders is significantly higher compared with the healthy patients which was reported as approximately one-third of SLE patients were proved as obesity. Notably, current focus is shifting to implementing cardio-metabolic protective strategies as well as elucidating underlying mechanisms of lupus-mediated obese status. On the other hand, adipocyte, as the most abundant endocrine cell in fat tissue, are dysfunctional in obese individuals with aberrant secretion of adipokines. It is proposing that the adipokine might link the pathology of cardio-metabolic disorders and SLE, whereas the related mechanism is complicated. In the current review, the functions of adipokine and the potential mechanisms by which the adipokine link cardio-metabolic disorders and SLE was well listed. Furthermore, the recommendations, which identify the adipokine as the potential therapeutic targets for the treatment of cardio-metabolic disorders and SLE, were also summarized.

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脂肪细胞分泌多种细胞因子与心脏代谢紊乱和SLE的关系。
系统性红斑狼疮(SLE)是一种多因素自身免疫介导的疾病,免疫细胞特别是T淋巴细胞受到过度刺激。这种方法可能导致多组织、多器官的系统性损伤。此外,SLE还与多种心脏代谢合并症相关,包括血脂异常、胰岛素抵抗和高血压。值得注意的是,与健康患者相比,心脏代谢紊乱的风险明显更高,据报道,大约三分之一的SLE患者被证实为肥胖。值得注意的是,目前的重点正在转移到实施心脏代谢保护策略以及阐明狼疮介导的肥胖状态的潜在机制。另一方面,脂肪细胞作为脂肪组织中最丰富的内分泌细胞,在肥胖个体中功能失调,脂肪因子分泌异常。提示脂肪因子可能与心脏代谢紊乱和SLE的病理相关,但相关机制较为复杂。本文综述了脂肪因子的功能以及脂肪因子与心脏代谢疾病和SLE相关的潜在机制。此外,还总结了将脂肪因子确定为治疗心脏代谢紊乱和SLE的潜在治疗靶点的建议。
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