Tu Lei, Yang Lijing
Division of Gastroenterology, Union Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, China.
Department of Radiation and Medical Oncology, Zhongnan Hospital, Wuhan University, Wuhan, China.
Front Endocrinol (Lausanne). 2019 Jan 30;10:26. doi: 10.3389/fendo.2019.00026. eCollection 2019.
As a cytokine in interleukin-1(IL-1) family, interleukin-33(IL-33) usually exists in the cytoplasm and cell nucleus. When the cells are activated or damaged, IL-33 can be secreted into extracellular and regulate the functions of various immune cells through binding to its specific receptor suppression of tumorigenicity 2 (ST2). Except regulating the function of immune cells including T cells, B cells, dendritic cells (DCs), macrophages, mast cells, and innate lymphoid cells, IL-33 also plays an important role in metabolic diseases and has received an increasing attention. This review summarizes the regulation of IL-33 on different immune cells in lipid metabolism, which will help to understand the pathology of abnormal lipid metabolic diseases, such as atherosclerosis and type 2 diabetes.
作为白细胞介素-1(IL-1)家族中的一种细胞因子,白细胞介素-33(IL-33)通常存在于细胞质和细胞核中。当细胞被激活或受损时,IL-33可分泌到细胞外,并通过与它的特异性受体2型抑瘤蛋白(ST2)结合来调节各种免疫细胞的功能。除了调节包括T细胞、B细胞、树突状细胞(DC)、巨噬细胞、肥大细胞和固有淋巴细胞在内的免疫细胞功能外,IL-33在代谢性疾病中也发挥着重要作用,并日益受到关注。本综述总结了IL-33对脂质代谢中不同免疫细胞的调节作用,这将有助于理解脂质代谢异常疾病如动脉粥样硬化和2型糖尿病的病理机制。