King Peter H, Chen Ching-Yi
1 Department of Neurology, University of Alabama at Birmingham , Birmingham, Alabama.
J Interferon Cytokine Res. 2014 Apr;34(4):267-74. doi: 10.1089/jir.2013.0143.
Cytokines and chemokines are key participants in pathways that drive inflammatory, immune, and other cellular responses to exogenous insults such as infection, trauma, and physiological stress. Persistent and aberrant expression of these factors has been linked to autoimmune, degenerative, and neoplastic diseases. Consequently, cytokine and chemokine expression is tightly governed at each level of gene regulation. Recent studies have demonstrated a role for KH-type splicing regulatory protein (KSRP) in curtailing cytokine and chemokine expression through transcriptional and post-transcriptional mechanisms, including promotion of microRNA maturation. Understanding the role of KSRP in cytokine mRNA metabolism should identify promising targets for the modulation of immune and inflammatory responses.
细胞因子和趋化因子是驱动炎症、免疫及其他细胞对外源损伤(如感染、创伤和生理应激)产生反应的信号通路中的关键参与者。这些因子的持续异常表达与自身免疫性疾病、退行性疾病和肿瘤性疾病有关。因此,细胞因子和趋化因子的表达在基因调控的各个层面都受到严格控制。最近的研究表明,KH型剪接调节蛋白(KSRP)通过转录和转录后机制(包括促进微小RNA成熟)在抑制细胞因子和趋化因子表达中发挥作用。了解KSRP在细胞因子mRNA代谢中的作用,应能确定调节免疫和炎症反应的有前景的靶点。