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C-C 趋化因子受体 7 通过β2 整合素促进 T 细胞急性淋巴细胞白血病侵犯中枢神经系统。

C-C Chemokine Receptor 7 Promotes T-Cell Acute Lymphoblastic Leukemia Invasion of the Central Nervous System via β2-Integrins.

机构信息

Department of Biological Sciences, The University of Texas at El Paso, El Paso, TX 79936, USA.

Public Health Sciences, The University of Texas at El Paso, El Paso, TX 79968, USA.

出版信息

Int J Mol Sci. 2024 Sep 6;25(17):9649. doi: 10.3390/ijms25179649.

Abstract

C-C Chemokine Receptor 7 (CCR7) mediates T-cell acute lymphoblastic leukemia (T-ALL) invasion of the central nervous system (CNS) mediated by chemotactic migration to C-C chemokine ligand 19 (CCL19). To determine if a CCL19 antagonist, CCL19, could inhibit CCR7-induced chemotaxis and signaling via CCL19 but not CCL21, we used transwell migration and Ca mobilization signaling assays. We found that in response to CCL19, human T-ALL cells employ β2 integrins to invade human brain microvascular endothelial cell monolayers. In vivo, using an inducible mouse model of T-ALL, we found that we were able to increase the survival of the mice treated with CCL19 when compared to non-treated controls. Overall, our results describe a targetable cell surface receptor, CCR7, which can be inhibited to prevent β2-integrin-mediated T-ALL invasion of the CNS and potentially provides a platform for the pharmacological inhibition of T-ALL cell entry into the CNS.

摘要

C-C 趋化因子受体 7(CCR7)介导 T 细胞急性淋巴细胞白血病(T-ALL)向中枢神经系统(CNS)的侵袭,通过趋化性迁移到 C-C 趋化因子配体 19(CCL19)介导。为了确定 CCL19 拮抗剂 CCL19 是否可以通过 CCL19 而不是 CCL21 抑制 CCR7 诱导的趋化性和信号转导,我们使用了 Transwell 迁移和 Ca 动员信号转导测定法。我们发现,在 CCL19 的作用下,人 T-ALL 细胞利用β2 整合素侵袭人脑微血管内皮细胞单层。在体内,使用可诱导的 T-ALL 小鼠模型,我们发现与未治疗的对照组相比,用 CCL19 治疗的小鼠的存活率增加。总的来说,我们的研究结果描述了一个可靶向的细胞表面受体 CCR7,它可以被抑制以防止β2 整合素介导的 T-ALL 对 CNS 的侵袭,并可能为药理学抑制 T-ALL 细胞进入 CNS 提供一个平台。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8d58/11395280/a14a76db8f80/ijms-25-09649-g001.jpg

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