School of Molecular and Cellular Biology, Faculty of Biological Sciences, and.
Division of Haematology and Immunology, Leeds Institute for Medical Research, St. James's University Hospital, University of Leeds, Leeds, United Kingdom.
Blood Adv. 2021 Apr 13;5(7):1922-1932. doi: 10.1182/bloodadvances.2020002402.
Calreticulin (CALR) is mutated in the majority of JAK2/MPL-unmutated myeloproliferative neoplasms (MPNs). Mutant CALR (CALRdel52) exerts its effect by binding to the thrombopoietin receptor MPL to cause constitutive activation of JAK-STAT signaling. In this study, we performed an extensive mutagenesis screen of the CALR globular N-domain and revealed 2 motifs critical for CALRdel52 oncogenic activity: (1) the glycan-binding lectin motif and (2) the zinc-binding domain. Further analysis demonstrated that the zinc-binding domain was essential for formation of CALRdel52 multimers, which was a co-requisite for MPL binding. CALRdel52 variants incapable of binding zinc were unable to homomultimerize, form CALRdel52-MPL heteromeric complexes, or stimulate JAK-STAT signaling. Finally, treatment with zinc chelation disrupted CALRdel52-MPL complexes in hematopoietic cells in conjunction with preferential eradication of cells expressing CALRdel52 relative to cells expressing other MPN oncogenes. In addition, zinc chelators exhibited a therapeutic effect in preferentially impairing growth of CALRdel52-mutant erythroblasts relative to unmutated erythroblasts in primary cultures of MPN patients. Together, our data implicate zinc as an essential cofactor for CALRdel52 oncogenic activity by enabling CALRdel52 multimerization and interaction with MPL, and suggests that perturbation of intracellular zinc levels may represent a new approach to abrogate the oncogenic activity of CALRdel52 in the treatment of MPNs.
钙网蛋白(CALR)在大多数 JAK2/MPL 未突变的骨髓增殖性肿瘤(MPN)中发生突变。突变型钙网蛋白(CALRdel52)通过与血小板生成素受体 MPL 结合发挥作用,导致 JAK-STAT 信号的组成性激活。在这项研究中,我们对 CALR 球形 N 结构域进行了广泛的诱变筛选,揭示了对 CALRdel52 致癌活性至关重要的 2 个基序:(1)糖结合凝集素基序和(2)锌结合域。进一步分析表明,锌结合域对于 CALRdel52 多聚体的形成是必需的,这是与 MPL 结合的共同要求。不能结合锌的 CALRdel52 变体无法同源多聚化,形成 CALRdel52-MPL 异源二聚体复合物,或刺激 JAK-STAT 信号。最后,锌螯合剂处理破坏了造血细胞中的 CALRdel52-MPL 复合物,同时优先清除表达 CALRdel52 的细胞,相对于表达其他 MPN 癌基因的细胞。此外,锌螯合剂在优先损害 CALRdel52 突变型红细胞的生长方面表现出治疗效果,相对于 MPN 患者原代培养中的未突变红细胞。总之,我们的数据表明,锌通过使 CALRdel52 多聚化并与 MPL 相互作用,作为 CALRdel52 致癌活性的必需辅助因子,提示干扰细胞内锌水平可能代表一种新方法,以消除 CALRdel52 在 MPN 治疗中的致癌活性。