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NKL 同源盒基因在 B 细胞发育和淋巴瘤中的活性。

NKL homeobox gene activities in B-cell development and lymphomas.

机构信息

Department of Human and Animal Cell Lines, Leibniz-Institute DSMZ-German Collection of Microorganisms and Cell Cultures, Braunschweig, Germany.

出版信息

PLoS One. 2018 Oct 11;13(10):e0205537. doi: 10.1371/journal.pone.0205537. eCollection 2018.

Abstract

Homeobox genes encode transcription factors which regulate basic processes in development and cell differentiation. Several members of the NKL subclass are deregulated in T-cell progenitors and support leukemogenesis. We have recently described particular expression patterns of nine NKL homeobox genes in early hematopoiesis and T-cell development. Here, we screened NKL homeobox gene activities in normal B-cell development and extended the NKL-code to include this lymphoid lineage. Analysis of public expression profiling datasets revealed that HHEX and NKX6-3 were the only members differentially active in naïve B-cells, germinal center B-cells, plasma cells and memory B-cells. Subsequent examination of different types of B-cell malignancies showed both aberrant overexpression of NKL-code members and ectopic activation of subclass members physiologically silent in lymphopoiesis including BARX2, DLX1, EMX2, NKX2-1, NKX2-2 and NKX3-2. Based on these findings we performed detailed studies of the B-cell specific NKL homeobox gene NKX6-3 which showed enhanced activity in patient subsets of follicular lymphoma, mantle cell lymphoma and diffuse large B-cell lymphoma (DLBCL), and in three DLBCL cell lines to serve as in vitro models. While excluding genomic and chromosomal rearrangements at the locus of NKX6-3 (8p11) promoter studies demonstrated that B-cell factors MYB and PAX5 activated NKX6-3 transcription. Furthermore, aberrant BMP7/SMAD1-signalling and deregulated expression of chromatin complex components AUTS2 and PCGF5 promoted NKX6-3 activation. Finally, NKL homeobox genes HHEX, HLX, MSX1 and NKX6-3 were expressed in B-cell progenitors and generated a regulatory gene network in cell lines which we propose may provide physiological support for NKL-code formation in early B-cell development. Together, we identified an NKL-code in B-cell development whose violation may deregulate differentiation and promote malignant transformation.

摘要

同源盒基因编码转录因子,调节发育和细胞分化的基本过程。NKL 亚类的几个成员在 T 细胞祖细胞中失调,支持白血病发生。我们最近描述了早期造血和 T 细胞发育中九个 NKL 同源盒基因的特定表达模式。在这里,我们筛选了正常 B 细胞发育中 NKL 同源盒基因的活性,并将 NKL 编码扩展到包括这个淋巴谱系。分析公共表达谱数据集显示,HHEX 和 NKX6-3 是幼稚 B 细胞、生发中心 B 细胞、浆细胞和记忆 B 细胞中唯一差异表达的成员。随后对不同类型的 B 细胞恶性肿瘤的检查显示,NKL 编码成员的异常过表达和生理上沉默在淋巴发生中的亚类成员的异位激活,包括 BARX2、DLX1、EMX2、NKX2-1、NKX2-2 和 NKX3-2。基于这些发现,我们对 B 细胞特异性 NKL 同源盒基因 NKX6-3 进行了详细研究,结果表明该基因在滤泡性淋巴瘤、套细胞淋巴瘤和弥漫性大 B 细胞淋巴瘤(DLBCL)患者亚群以及三个 DLBCL 细胞系中活性增强,可作为体外模型。虽然排除了 NKX6-3(8p11)基因座的基因组和染色体重排,启动子研究表明 B 细胞因子 MYB 和 PAX5 激活了 NKX6-3 转录。此外,异常的 BMP7/SMAD1 信号和染色质复合物成分 AUTS2 和 PCGF5 的表达失调促进了 NKX6-3 的激活。最后,NKL 同源盒基因 HHEX、HLX、MSX1 和 NKX6-3 在 B 细胞祖细胞中表达,并在细胞系中生成了一个调节基因网络,我们提出该网络可能为早期 B 细胞发育中 NKL 编码的形成提供生理支持。总之,我们确定了 B 细胞发育中的 NKL 编码,其破坏可能会使分化失调并促进恶性转化。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/34c4/6181399/eea9de76fbce/pone.0205537.g001.jpg

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