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IFI16 表达与 B 细胞分化过程中的某些转录因子有关。

IFI16 Expression Is Related to Selected Transcription Factors during B-Cell Differentiation.

机构信息

Department of Experimental, Diagnostic, and Specialty Medicine, Bologna University Medical School Unit of Hematopathology, S. Orsola Malpighi Hospital, 40138 Bologna, Italy.

Department of Human Pathology, University of Palermo, 90127 Palermo, Italy.

出版信息

J Immunol Res. 2015;2015:747645. doi: 10.1155/2015/747645. Epub 2015 Jun 22.

Abstract

The interferon-inducible DNA sensor IFI16 is involved in the modulation of cellular survival, proliferation, and differentiation. In the hematopoietic system, IFI16 is consistently expressed in the CD34+ stem cells and in peripheral blood lymphocytes; however, little is known regarding its regulation during maturation of B- and T-cells. We explored the role of IFI16 in normal B-cell subsets by analysing its expression and relationship with the major transcription factors involved in germinal center (GC) development and plasma-cell (PC) maturation. IFI16 mRNA was differentially expressed in B-cell subsets with significant decrease in IFI16 mRNA in GC and PCs with respect to naïve and memory subsets. IFI16 mRNA expression is inversely correlated with a few master regulators of B-cell differentiation such as BCL6, XBP1, POU2AF1, and BLIMP1. In contrast, IFI16 expression positively correlated with STAT3, REL, SPIB, RELA, RELB, IRF4, STAT5B, and STAT5A. ARACNE algorithm indicated a direct regulation of IFI16 by BCL6, STAT5B, and RELB, whereas the relationship between IFI16 and the other factors is modulated by intermediate factors. In addition, analysis of the CD40 signaling pathway showed that IFI16 gene expression directly correlated with NF-κB activation, indicating that IFI16 could be considered an upstream modulator of NF-κB in human B-cells.

摘要

干扰素诱导 DNA 传感器 IFI16 参与细胞存活、增殖和分化的调节。在造血系统中,IFI16 在 CD34+干细胞和外周血淋巴细胞中持续表达;然而,关于其在 B 和 T 细胞成熟过程中的调节知之甚少。我们通过分析 IFI16 在生发中心 (GC) 发育和浆细胞 (PC) 成熟过程中涉及的主要转录因子的表达及其与 IFI16 的关系,探讨了 IFI16 在正常 B 细胞亚群中的作用。IFI16 mRNA 在 B 细胞亚群中差异表达,与幼稚和记忆亚群相比,GC 和 PCs 中的 IFI16 mRNA 显著减少。IFI16 mRNA 的表达与 B 细胞分化的几个主调控因子呈负相关,如 BCL6、XBP1、POU2AF1 和 BLIMP1。相比之下,IFI16 的表达与 STAT3、REL、SPIB、RELA、RELB、IRF4、STAT5B 和 STAT5A 呈正相关。ARACNE 算法表明,BCL6、STAT5B 和 RELB 直接调节 IFI16,而 IFI16 与其他因子之间的关系则受中间因子调节。此外,分析 CD40 信号通路表明,IFI16 基因表达与 NF-κB 激活直接相关,表明 IFI16 可被视为人类 B 细胞中 NF-κB 的上游调节剂。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0dc0/4491573/158e54fa683f/JIR2015-747645.001.jpg

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