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B淋巴细胞激酶在皮肤T细胞淋巴瘤中的异位表达。

Ectopic expression of B-lymphoid kinase in cutaneous T-cell lymphoma.

作者信息

Krejsgaard Thorbjørn, Vetter-Kauczok Claudia S, Woetmann Anders, Kneitz Hermann, Eriksen Karsten W, Lovato Paola, Zhang Qian, Wasik Mariusz A, Geisler Carsten, Ralfkiaer Elisabeth, Becker Juergen C, Ødum Niels

机构信息

Department of Biology, University of Copenhagen, Copenhagen, Denmark

出版信息

Blood. 2009 Jun 4;113(23):5896-904. doi: 10.1182/blood-2008-09-181024. Epub 2009 Apr 7.

Abstract

B-lymphoid kinase (Blk) is exclusively expressed in B cells and thymocytes. Interestingly, transgenic expression of a constitutively active form of Blk in the T-cell lineage of mice results in the development of T-lymphoid lymphomas. Here, we demonstrate nuclear factor-kappa B (NF-kappaB)-mediated ectopic expression of Blk in malignant T-cell lines established from patients with cutaneous T-cell lymphoma (CTCL). Importantly, Blk is also expressed in situ in lesional tissue specimens from 26 of 31 patients with CTCL. Already in early disease the majority of epidermotropic T cells express Blk, whereas Blk expression is not observed in patients with benign inflammatory skin disorders. In a longitudinal study of an additional 24 patients biopsied for suspected CTCL, Blk expression significantly correlated with a subsequently confirmed diagnosis of CTCL. Blk is constitutively tyrosine phosphorylated in malignant CTCL cell lines and spontaneously active in kinase assays. Furthermore, targeting Blk activity and expression by Src kinase inhibitors and small interfering RNA (siRNA) inhibit the proliferation of the malignant T cells. In conclusion, this is the first report of Blk expression in CTCL, thereby providing new clues to the pathogenesis of the disease.

摘要

B淋巴细胞激酶(Blk)仅在B细胞和胸腺细胞中表达。有趣的是,在小鼠的T细胞谱系中组成型激活形式的Blk的转基因表达会导致T淋巴细胞淋巴瘤的发生。在此,我们证明了核因子κB(NF-κB)介导的Blk在从皮肤T细胞淋巴瘤(CTCL)患者建立的恶性T细胞系中的异位表达。重要的是,在31例CTCL患者中的26例的病变组织标本中也原位表达了Blk。在疾病早期,大多数亲表皮性T细胞就表达Blk,而在良性炎症性皮肤病患者中未观察到Blk表达。在另外24例因疑似CTCL而接受活检的患者的纵向研究中,Blk表达与随后确诊的CTCL显著相关。在恶性CTCL细胞系中,Blk持续酪氨酸磷酸化,并且在激酶测定中具有自发活性。此外,通过Src激酶抑制剂和小干扰RNA(siRNA)靶向Blk活性和表达可抑制恶性T细胞的增殖。总之,这是关于Blk在CTCL中表达的首次报道,从而为该疾病的发病机制提供了新线索。

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