Department of Dermatology, Cutaneous Oncology Program, Beth Israel Deaconess Medical Center, Harvard Medical School, Boston, Massachusetts, USA.
J Clin Invest. 2011 Dec;121(12):4838-49. doi: 10.1172/JCI41769. Epub 2011 Nov 14.
Cutaneous T cell lymphomas (CTCLs) represent a heterogeneous group of non-Hodgkin lymphomas that affect the skin. The pathogenesis of these conditions is poorly understood. For example, the signaling mechanisms contributing to the dysregulated growth of the neoplastic T cells are not well defined. Here, we demonstrate that loss of nuclear localization of pro-IL-16 facilitates CTCL cell proliferation by causing a decrease in expression of the cyclin dependent-kinase inhibitor p27Kip1. The decrease in p27Kip1 expression was directly attributable to an increase in expression of S-phase kinase-associated protein 2 (Skp2). Regulation of Skp2 is in part attributed to the nuclear presence of the scaffold protein pro-IL-16. T cells isolated from 11 patients with advanced CTCL, but not those from healthy controls or patients with T cell acute lymphocytic leukemia (T-ALL), demonstrated reduction in nuclear pro-IL-16 levels. Sequence analysis identified the presence of mutations in the 5' end of the PDZ1 region of pro-IL-16, a domain required for association of pro-IL-16 with the nuclear chaperone HSC70 (also known as HSPA8). HSC70 knockdown led to loss of nuclear translocation by pro-IL-16 and subsequent increases in Skp2 levels and decreases in p27Kip1 levels, which ultimately enhanced T cell proliferation. Thus, our data indicate that advanced CTCL cell growth is facilitated, at least in part, by mutations in the scaffold protein pro-IL-16, which directly regulates Skp2 synthesis.
皮肤 T 细胞淋巴瘤(CTCLs)是一组影响皮肤的非霍奇金淋巴瘤的异质性群体。这些疾病的发病机制尚未完全清楚。例如,导致肿瘤性 T 细胞异常生长的信号机制尚未得到很好的定义。在这里,我们证明了前白细胞介素-16(pro-IL-16)的核定位缺失通过降低细胞周期蛋白依赖性激酶抑制剂 p27Kip1 的表达促进 CTCL 细胞增殖。p27Kip1 表达的降低直接归因于 S 期激酶相关蛋白 2(Skp2)表达的增加。Skp2 的调节部分归因于支架蛋白 pro-IL-16 的核存在。从 11 例晚期 CTCL 患者中分离出的 T 细胞,但不是从健康对照者或 T 细胞急性淋巴细胞白血病(T-ALL)患者中分离出的 T 细胞,表现出核 pro-IL-16 水平降低。序列分析确定了前白细胞介素-16 的 PDZ1 区域 5'端存在突变,该区域是 pro-IL-16 与核伴侣 HSC70(也称为 HSPA8)结合所必需的。HSC70 的敲低导致 pro-IL-16 的核易位丧失,随后 Skp2 水平升高和 p27Kip1 水平降低,最终增强了 T 细胞增殖。因此,我们的数据表明,至少部分是由支架蛋白 pro-IL-16 的突变促进了晚期 CTCL 细胞的生长,该突变直接调节 Skp2 的合成。