Yuan Ming-Jie, Wang Tao
Department of Cardiology, Renmin Hospital of Wuhan University, Wuhan, Hubei 430060, P.R. China.
Cardiovascular Research Center, University of Virginia, Charlottesville, VA 22908, USA.
Biomed Rep. 2016 Jul;5(1):3-6. doi: 10.3892/br.2016.665. Epub 2016 Apr 27.
Interleukin-21 (IL-21) and its receptor (IL-21R) are broadly expressed on human B cells, activated T cells and other myeloid cells. IL-21 cooperates with IL-6 and transforming growth factor-β to regulate T-cell differentiation. IL-21-mediated human B cell and dendritic cells differentiation requires signal transducer and activator of transcription 3 (STAT3), and also induces B-cell apoptosis dependents on the Toll-like receptor signal. Recently, and experiments showed that IL-21/IL-21R regulate angiogenesis through STAT3. IL-21 signaling pathways are complex due to its cooperation with other transcriptional factors, such as interferon regulatory factor 4 and granulocyte-macrophage colony-stimulating factor. The Janus kinase-STAT pathway has been the most extensively studied. With the increase in the understanding of IL-21 biology in the context of each specific disease or pathological condition, IL-21 could be a new therapeutic target for immune-related disease.
白细胞介素-21(IL-21)及其受体(IL-21R)在人类B细胞、活化的T细胞和其他髓系细胞上广泛表达。IL-21与IL-6和转化生长因子-β协同作用以调节T细胞分化。IL-21介导的人类B细胞和树突状细胞分化需要信号转导和转录激活因子3(STAT3),并且还依赖Toll样受体信号诱导B细胞凋亡。最近,实验表明IL-21/IL-21R通过STAT3调节血管生成。由于IL-21与其他转录因子(如干扰素调节因子4和粒细胞-巨噬细胞集落刺激因子)协同作用,其信号通路较为复杂。Janus激酶-STAT途径是研究最为广泛的。随着在每种特定疾病或病理状况背景下对IL-21生物学认识的增加,IL-21可能成为免疫相关疾病的新治疗靶点。