RBPJ/PAF1信号轴通过NOTCH信号传导促进阵发性夜间血红蛋白尿的克隆扩展

Liyan Li, Junshu Wu, Zewei Chen, Hui Liu, Zhaoyun Liu, Yingying Chen, Honglei Wang, Rong Fu
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引用次数: 0

摘要

背景:阵发性夜间血红蛋白尿(PNH)的发病机制与除猪- a外的其他体细胞突变密切相关。我们前期研究通过全基因组外显子测序发现部分PNH患者存在RBPJ高频突变,该突变在PNH发病中发挥重要作用,但其分子机制尚不清楚。方法:采用SiRNA转染制备rbpj基因敲低的K562和PNH细胞系。分别用EDU和流式细胞术检测细胞增殖和凋亡。银染色后的LC-MS鉴定出rbpj相互作用蛋白,随后使用CO-IP和梯度表达分析对其进行验证。Western blot检测低表达RBPJ的PNH细胞系中RBPJ、PAF1和NOTCH信号通路之间的关系。分析PAF1表达与克隆PNH、RBPJ表达的相关性。结果:敲除RBPJ可使PNH细胞增殖减少,凋亡增加。我们发现PAF1是RBPJ的一个相互作用蛋白,并确定其相互作用结构域为RBPJ的BTD结构域。敲除RBPJ导致KO细胞株中PAF1蛋白表达减少,而与NOTCH信号相关的NOTCH1和HEY1蛋白表达减少。GSEA表明,KO细胞系在PAF1下调后表现出NOTCH信号通路的减少。敲除PAF1导致NOTCH1和NOTCH2蛋白水平降低。随后,PAF1过表达敲除RBPJ后,NOTCH1表达恢复,细胞凋亡率降低,细胞增殖增加。随后,我们观察到PAF1在PNH患者中的表达升高,并与PNH患者中FLAER-CD14、FLAER-CD24和RBPJ mRNA的表达呈正相关。结论:RBPJ/PAF1可能通过调控NOTCH信号通路促进PNH克隆增殖。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
RBPJ/PAF1 Signaling Axis Promotes Cloning Expansion in Paroxysmal Nocturnal Hemoglobinuria Through NOTCH Signaling.

Background: The pathogenesis of paroxysmal nocturnal hemoglobinuria (PNH) is closely related to additional somatic mutations besides PIG-A. Our previous research showed that some PNH patients had a high frequency mutation of RBPJ through whole genome exon sequencing, which played an important role in the pathogenesis of PNH, but its molecular mechanism is still unclear.

Methods: SiRNA transfection was employed to generate RBPJ-knockdown K562 and PNH cell lines. Cell proliferation and apoptosis were assessed via EDU and flow cytometry, respectively. LC-MS following silver staining identified RBPJ-interacting proteins, which were subsequently validated using CO-IP and gradient expression analysis. Western blot examined the relationship between RBPJ, PAF1, and the NOTCH signaling pathway in low-RBPJ-expressing PNH cell lines. The correlation between PAF1 expression, clonal PNH, and RBPJ expression was also analyzed.

Results: Knocking Out RBPJ Leads to Reduced Cell Proliferation and Increased Apoptosis in PNH Cells. We Identified PAF1 as an Interacting Protein of RBPJ and Confirmed the Interaction Domain to Be the BTD Domain of RBPJ. Knocking Out RBPJ Resulted in a Decrease of PAF1 Protein in KO Cell Lines, While the NOTCH1 and HEY1 Protein Expression Related to the NOTCH Signaling Decreased. GSEA Demonstrated That the KO Cell Lines Exhibited a Decreased NOTCH Signaling Pathway Upon PAF1 Downregulation. Knocking Down PAF1 Results in Reduced Protein Levels of NOTCH1 and NOTCH2. Subsequently, After Knocking Out RBPJ With PAF1 Overexpression, NOTCH1 Expression Was Restored, Cell Apoptosis Rate Decreased, and Cell Proliferation Increased. Subsequently, we Observed Elevated PAF1 Expression in PNH Patients, Which Positively Correlated With the FLAER-CD14, FLAER-CD24 and RBPJ mRNA Expression in PNH Patients.

Conclusion: RBPJ/PAF1 may promote PNH clone proliferation by regulating the NOTCH signaling pathway.

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