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对正常B细胞晚期分化阶段中涉及的微小RNA的鉴定表明,微小RNA靶标ZEB1和TP53发挥着核心作用。

Identification of microRNAs implicated in the late differentiation stages of normal B cells suggests a central role for miRNA targets ZEB1 and TP53.

作者信息

Malpeli Giorgio, Barbi Stefano, Zupo Simonetta, Tosadori Gabriele, Scardoni Giovanni, Bertolaso Anna, Sartoris Silvia, Ugel Stefano, Vicentini Caterina, Fassan Matteo, Adamo Annalisa, Krampera Mauro, Scupoli Maria Teresa, Croce Carlo Maria, Scarpa Aldo

机构信息

Department of Surgical Sciences, Dentistry, Gynecology and Pediatrics, Section of Surgery, University of Verona, Verona, Italy.

Department of Diagnostics and Public Health, Section of Pathological Anatomy, University of Verona, Verona, Italy.

出版信息

Oncotarget. 2017 Feb 14;8(7):11809-11826. doi: 10.18632/oncotarget.14683.

Abstract

In the late B cell differentiation stages, miRNAs expression modifications promoting or inhibiting key pathways are only partially defined. We isolated 29 CD19+ human B cell samples at different stages of differentiation: B cells from peripheral blood; naïve, germinal center (GC) and subepithelial (SE) B cells from tonsils. SE cells were further split in activated and resting B cell. The miRNA expression profile of these B cells was assessed by microarray analysis and selected miRNAs were validated by quantitative RT-PCR and in situ hybridization on normal tonsils. The comparison of all samples showed changes in 107 miRNAs in total. Among 48 miRNAs differentially expressed in naïve, GC and SE cells, we identified 8 miRNAs: mir-323, mir-138, mir-9*, mir-211, mir-149, mir-373, mir-135a and mir-184, strictly specific to follicular cells that had never been implicated before in late stages of B cell development. Moreover, we unveiled 34 miRNAs able to discriminate between CD5- activated B cells and resting B cells. The miRNAs profile of CD5- resting B cells showed a higher similarity to naïve CD5+ than CD5- activated B cells. Finally, network analysis on shortest paths connecting gene targets suggested ZEB1 and TP53 as key miRNA targets during the follicular differentiation pathway. These data confirm and extend our knowledge on the miRNAs-related regulatory pathways involved in the late B cell maturation.

摘要

在B细胞分化后期,促进或抑制关键通路的微小RNA(miRNA)表达修饰仅得到部分界定。我们分离了29个处于不同分化阶段的人CD19⁺ B细胞样本:外周血B细胞;扁桃体中的幼稚、生发中心(GC)和上皮下(SE)B细胞。SE细胞进一步分为活化B细胞和静息B细胞。通过微阵列分析评估这些B细胞的miRNA表达谱,并通过定量逆转录聚合酶链反应(RT-PCR)和在正常扁桃体上进行原位杂交对选定的miRNA进行验证。对所有样本的比较显示,总共107个miRNA发生了变化。在幼稚、GC和SE细胞中差异表达的48个miRNA中,我们鉴定出8个miRNA:mir-323、mir-138、mir-9*、mir-211、mir-149、mir-373、mir-135a和mir-184,它们严格特异性地表达于滤泡细胞,此前从未被认为与B细胞发育后期有关。此外,我们发现34个miRNA能够区分CD5⁻活化B细胞和静息B细胞。CD5⁻静息B细胞的miRNA谱与幼稚CD5⁺ B细胞的相似性高于CD5⁻活化B细胞。最后,对连接基因靶点的最短路径进行网络分析表明,ZEB1和TP53是滤泡分化途径中关键的miRNA靶点。这些数据证实并扩展了我们对参与B细胞后期成熟的miRNA相关调控通路的认识。

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