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在慢性淋巴细胞白血病细胞中,功能性1-磷酸鞘氨醇受体-1的表达受B细胞受体信号传导的抑制,而通过抑制PI3激酶δ可使其表达增加,但抑制脾酪氨酸激酶(SYK)或布鲁顿酪氨酸激酶(BTK)则不会增加其表达。

Expression of functional sphingosine-1 phosphate receptor-1 is reduced by B cell receptor signaling and increased by inhibition of PI3 kinase δ but not SYK or BTK in chronic lymphocytic leukemia cells.

作者信息

Till Kathleen J, Pettitt Andrew R, Slupsky Joseph R

机构信息

Department of Molecular and Clinical Cancer Medicine, University of Liverpool, Liverpool L69 3GA, United Kingdom

Department of Molecular and Clinical Cancer Medicine, University of Liverpool, Liverpool L69 3GA, United Kingdom.

出版信息

J Immunol. 2015 Mar 1;194(5):2439-46. doi: 10.4049/jimmunol.1402304. Epub 2015 Jan 28.

Abstract

BCR signaling pathway inhibitors such as ibrutinib, idelalisib, and fostamatinib (respective inhibitors of Bruton's tyrosine kinase, PI3Kδ, and spleen tyrosine kinase) represent a significant therapeutic advance in B cell malignancies, including chronic lymphocytic leukemia (CLL). These drugs are distinctive in increasing blood lymphocytes while simultaneously shrinking enlarged lymph nodes, suggesting anatomical redistribution of CLL cells from lymph nodes into the blood. However, the mechanisms underlying this phenomenon are incompletely understood. In this study, we showed that the egress receptor, sphingosine-1-phosphate (S1P) receptor 1 (S1PR1), was expressed at low levels in normal germinal centers and CLL lymph nodes in vivo but became upregulated on normal B cells and, to a variable and lesser extent, CLL cells following in vitro incubation in S1P-free medium. Spontaneous recovery of S1PR1 expression on normal B and CLL cells was prevented by BCR cross-linking, whereas treatment of CLL cells with idelalisib increased S1PR1 expression and migration toward S1P, the greatest increase occurring in cases with unmutated IgH V region genes. Intriguingly, ibrutinib and fostamatinib had no effect on S1PR1 expression or function. Conversely, chemokine-induced migration, which requires integrin activation and is essential for the entry of lymphocytes into lymph nodes as well as their retention, was blocked by ibrutinib and fostamatinib, but not idelalisib. In summary, our results suggest that different BCR signaling inhibitors redistribute CLL cells from lymph nodes into the blood through distinct mechanisms: idelalisib actively promotes egress by upregulating S1PR1, whereas fostamatinib and ibrutinib may reduce CLL cell entry and retention by suppressing chemokine-induced integrin activation.

摘要

布鲁顿酪氨酸激酶(BTK)抑制剂依鲁替尼、idelalisib和福司替尼(分别为布鲁顿酪氨酸激酶、PI3Kδ和脾酪氨酸激酶的抑制剂)等BCR信号通路抑制剂代表了B细胞恶性肿瘤治疗方面的重大进展,包括慢性淋巴细胞白血病(CLL)。这些药物的独特之处在于,它们在增加血液淋巴细胞数量的同时,能使肿大的淋巴结缩小,这表明CLL细胞从淋巴结向血液发生了解剖学上的重新分布。然而,这一现象背后的机制尚未完全明确。在本研究中,我们发现,流出受体——1-磷酸鞘氨醇(S1P)受体1(S1PR1)在体内正常生发中心和CLL淋巴结中的表达水平较低,但在正常B细胞以及体外在无S1P培养基中孵育后的CLL细胞(程度不一且较低)上会上调。BCR交联可阻止正常B细胞和CLL细胞上S1PR1表达的自发恢复,而用idelalisib治疗CLL细胞可增加S1PR1表达并使其向S1P迁移,在未突变的IgH V区基因病例中增加最为显著。有趣的是,依鲁替尼和福司替尼对S1PR1表达或功能没有影响。相反,趋化因子诱导的迁移需要整合素激活,对淋巴细胞进入淋巴结及其滞留至关重要,依鲁替尼和福司替尼可阻断这种迁移,但idelalisib不会。总之,我们的结果表明,不同的BCR信号抑制剂通过不同机制将CLL细胞从淋巴结重新分布到血液中:idelalisib通过上调S1PR1积极促进流出,而福司替尼和依鲁替尼可能通过抑制趋化因子诱导的整合素激活来减少CLL细胞的进入和滞留。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7baa/4337486/9d71f97d8600/JI_1402304_f1.jpg

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