Andersson Karin M E, Brisslert Mikael, Cavallini Nicola Filluelo, Svensson Mattias N D, Welin Amanda, Erlandsson Malin C, Ciesielski Michael J, Katona Gergely, Bokarewa Maria I
Department of Rheumatology and Inflammation Research, The Sahlgrenska Academy at University of Gothenburg, Gothenburg, Sweden.
Division of Cellular Biology, La Jolla Institute for Allergy & Immunology, La Jolla, CA, USA.
Oncotarget. 2015 Aug 21;6(24):20043-57. doi: 10.18632/oncotarget.4994.
Follicular T helper (Tfh) cells are recognized by the expression of CXCR5 and the transcriptional regulator Bcl-6. Tfh cells control B cell maturation and antibody production, and if deregulated, may lead to autoimmunity. Here, we study the role of the proto-oncogene survivin in the formation of Tfh cells. We show that blood Tfh cells of patients with the autoimmune condition rheumatoid arthritis, have intracellular expression of survivin. Survivin was co-localized with Bcl-6 in the nuclei of CXCR5+CD4 lymphocytes and was immunoprecipitated with the Bcl-6 responsive element of the target genes. Inhibition of survivin in arthritic mice led to the reduction of CXCR5+ Tfh cells and to low production of autoantibodies. Exposure to survivin activated STAT3 and induced enrichment of PD-1+Bcl-6+ subset within Tfh cells. Collectively, our study demonstrates that survivin belongs to the Tfh cell phenotype and ensures their optimal function by regulating transcriptional activity of Bcl-6.
滤泡辅助性T(Tfh)细胞通过CXCR5的表达和转录调节因子Bcl-6来识别。Tfh细胞控制B细胞成熟和抗体产生,若调节失控,可能导致自身免疫。在此,我们研究原癌基因survivin在Tfh细胞形成中的作用。我们发现,自身免疫性疾病类风湿关节炎患者的血液Tfh细胞中有survivin的细胞内表达。Survivin与Bcl-6在CXCR5+CD4淋巴细胞的细胞核中共定位,并与靶基因的Bcl-6反应元件进行免疫沉淀。抑制关节炎小鼠体内的survivin会导致CXCR5+ Tfh细胞减少以及自身抗体产生降低。暴露于survivin会激活STAT3并诱导Tfh细胞内PD-1+Bcl-6+亚群富集。总的来说,我们的研究表明survivin属于Tfh细胞表型,并通过调节Bcl-6的转录活性确保其最佳功能。