Department of Pathology, Zhangzhou Affiliated Hospital of Fujian Medical University, No. 59, Shengli West Road, Xiangcheng District, Zhangzhou 363000, Fujian, China.
Department of Basic Medicine, Zhangzhou Health Vocational College; Collaborative Innovation Center for Translation Medical Testing and Application Technology, No. 29, Shengli West Road, Xiangcheng District, Zhangzhou 363000, Fujian, China.
Integr Biol (Camb). 2024 Jan 23;16. doi: 10.1093/intbio/zyae021.
In B cells, the chemokine receptor CXCR3 is expressed only by a subset of B cells. However, CXCR3 is highly expressed in a rare type of B-cell lymphoma known as Mantle Cell Lymphoma (MCL) and CXCR3 inhibitor impairs proliferation and induces apoptosis in the MCL cell line JeKo-1. Despite this, the mechanism responsible for maintaining high levels of CXCR3 in MCL cells remains unclear. In this study, we assessed CXCR3 expression and amplification in MCL samples and confirmed that CXCR3 is overexpressed in MCL tissues. We also observed that CXCR3 amplification is present in a small portion of MCL patients and is associated with MCL classification. We then screened ubiquitin-specific proteases (USPs) that might control the degradation of CXCR3 protein. Our investigation revealed that USP35 acts as a potent stabilizer of CXCR3 protein. Knockdown of USP35 substantially reduced the CXCR3 protein levels in JeKo-1 cells, resulting in reduced cell viability, cell cycle arrest, increased apoptosis, and mitigated migration and invasion in these cells. At the molecular level, USP35 deubiquitinates and stabilizes CXCR3. USP35 deficiency attenuated the activation of the JAK1/STAT1 pathway and reduced the expression of β-catenin and c-Myc in JeKo-1 cells. Furthermore, we observed that overexpression of CXCR3 rescued the impaired tumorigenicity of USP35-deficient JeKo-1 cells, and the mechanism may be related to the fact that USP35 promotes CXCR3 deubiquitination to stabilize its expression. These findings collectively demonstrate the oncogenic role of the USP35-CXCR3 axis in JeKo-1 MCL cells.
在 B 细胞中,趋化因子受体 CXCR3 仅由 B 细胞的一个亚群表达。然而,CXCR3 在一种罕见的 B 细胞淋巴瘤——套细胞淋巴瘤(MCL)中高度表达,CXCR3 抑制剂可抑制 MCL 细胞系 JeKo-1 的增殖并诱导其凋亡。尽管如此,导致 MCL 细胞中 CXCR3 高水平表达的机制仍不清楚。在这项研究中,我们评估了 MCL 样本中 CXCR3 的表达和扩增,并证实 CXCR3 在 MCL 组织中过表达。我们还观察到,CXCR3 扩增存在于一小部分 MCL 患者中,并与 MCL 分类相关。然后,我们筛选了可能控制 CXCR3 蛋白降解的泛素特异性蛋白酶(USP)。我们的研究表明,USP35 是 CXCR3 蛋白的有效稳定剂。USP35 的敲低显著降低了 JeKo-1 细胞中的 CXCR3 蛋白水平,导致细胞活力降低、细胞周期停滞、凋亡增加,并减轻了这些细胞的迁移和侵袭能力。在分子水平上,USP35 去泛素化并稳定 CXCR3。USP35 缺乏可减弱 JAK1/STAT1 途径的激活,并降低 JeKo-1 细胞中 β-连环蛋白和 c-Myc 的表达。此外,我们观察到,CXCR3 的过表达挽救了 USP35 缺陷的 JeKo-1 细胞中受损的致瘤性,其机制可能与 USP35 促进 CXCR3 去泛素化以稳定其表达有关。这些发现共同表明,USP35-CXCR3 轴在 JeKo-1 MCL 细胞中具有致癌作用。