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MicroRNA-100-5p indirectly modulates the expression of Il6 Ptgs1/2 and Tlr4 mRNA in the mouse follicular dendritic cell-like cell line FL-Y

机译:MicroRNA-100-5p间接调节小鼠滤泡树突状细胞样细胞系FL-Y中Il6Ptgs1 / 2和Tlr4 mRNA的表达

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摘要

Follicular dendritic cells (FDC) are important stromal cells within the B-cell follicles and germinal centres (GC) of secondary lymphoid tissues. FDC trap and retain native antigens on their surfaces in the form of immune complexes that they display to B cells, in order to select those cells with the highest antigen affinity. MicroRNAs are short, non-coding RNAs that are approximately 18–25 nucleotides in length that regulate gene expression at the post-transcriptional level by repressing the translation of target genes. In the current study, in vivo and in vitro systems were used to identify microRNAs that were potentially expressed by FDC. Constitutive lymphotoxin-β receptor (LTβR) stimulation is required to maintain FDC in their differentiated state. We show that the rapid de-differentiation of spleen FDC that accompanied LTβR-blockade, coincided with a significant decrease in the expression of mmu-miR-100-5p, mmu-miR-138-5p and mmu-miR-2137. These microRNAs were shown to be expressed in the FDC-like cell line, FL-YB, and specific inhibition of mmu-miR-100-5p significantly enhanced expression of Il6, Ptgs1/2 and Tlr4 mRNA in this cell line. The expression of Il6, Ptgs1/2 and Tlr4 by FDC play important roles in regulating GC size and promoting high-affinity antibody responses, so it is plausible that mmu-miR-100-5p may help to regulate the expression of these genes during GC reactions.
机译:滤泡树突状细胞(FDC)是继发性淋巴组织的B细胞滤泡和生发中心(GC)内的重要基质细胞。 FDC以展示给B细胞的免疫复合物的形式捕获并保留天然抗原在其表面,以选择具有最高抗原亲和力的细胞。 MicroRNA是短的非编码RNA,长度约为18–25个核苷酸,可通过抑制靶基因的翻译来调节转录后水平的基因表达。在当前的研究中,体内和体外系统用于鉴定可能由FDC表达的microRNA。需要组成型淋巴毒素-β受体(LTβR)刺激才能将FDC维持在其分化状态。我们显示,伴随LTβR阻断的脾脏FDC的快速去分化,与mmu-miR-100-5p,mmu-miR-138-5p和mmu-miR-2137的表达显着降低相吻合。这些microRNA已显示在FDC样细胞系FL-YB中表达,对mmu-miR-100-5p的特异性抑制显着增强了该细胞系中Il6,Ptgs1 / 2和Tlr4 mRNA的表达。 FDC的Il6,Ptgs1 / 2和Tlr4的表达在调节GC大小和促进高亲和力抗体反应中起重要作用,因此mmu-miR-100-5p可能有助于在GC期间调节这些基因的表达。反应。

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