Kwon Oh Chan, Kim Soohyun, Hong Seokchan, Lee Chang-Keun, Yoo Bin, Chang Eun-Ju, Kim Yong-Gil
Division of Rheumatology, Department of Internal Medicine, Asan Medical Center, University of Ulsan College of Medicine, Seoul 05505, Korea.
Department of Biomedical Science and Technology, Konkuk University, Seoul 05066, Korea.
Immune Netw. 2018 Jun 9;18(3):e20. doi: 10.4110/in.2018.18.e20. eCollection 2018 Jun.
IL-32 acts as a pro-inflammatory cytokine by inducing the synthesis of inflammatory molecules as well as promoting the morphological changes involved in the transformation of monocytes into osteoclasts (OCs). Evaluation of the functions of IL-32 has mainly focused on its inflammatory properties, such as involvement in the pathogenesis of various autoimmune diseases. Recently, IL-32 was shown to be involved in bone metabolism, in which it promotes the differentiation and activation of OCs and plays a key role in bone resorption in inflammatory conditions. IL-32γ also regulates bone formation in conditions such as ankylosing spondylitis and osteoporosis. In this review, we summarize the results of recent studies on the role of IL-32γ in bone metabolism in inflammatory arthritis.
白细胞介素-32(IL-32)通过诱导炎症分子的合成以及促进单核细胞向破骨细胞(OCs)转化过程中涉及的形态学变化,发挥促炎细胞因子的作用。对IL-32功能的评估主要集中在其炎症特性上,例如参与各种自身免疫性疾病的发病机制。最近,研究表明IL-32参与骨代谢,它在其中促进OCs的分化和激活,并在炎症条件下的骨吸收中起关键作用。IL-32γ在强直性脊柱炎和骨质疏松症等病症中也调节骨形成。在本综述中,我们总结了近期关于IL-32γ在炎症性关节炎骨代谢中作用的研究结果。