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脉络丛基质构成了小儿 B 细胞前体急性淋巴细胞白血病中枢神经系统的避难所。

The choroid plexus stroma constitutes a sanctuary for paediatric B-cell precursor acute lymphoblastic leukaemia in the central nervous system.

机构信息

Department of Cell Biology, School of Medicine, Complutense University, Madrid, Spain.

School of Chemistry, Autonomous University of Chihuahua, Chihuahua, Mexico.

出版信息

J Pathol. 2020 Oct;252(2):189-200. doi: 10.1002/path.5510. Epub 2020 Aug 28.

Abstract

Despite current central nervous system-directed therapies for childhood B-cell precursor acute lymphoblastic leukaemia, relapse at this anatomical site still remains a challenging issue. Few reports have addressed the study of the specific cellular microenvironments which can promote the survival, quiescence, and therefore chemoresistance of B-cell precursor acute lymphoblastic leukaemia cells in the central nervous system. Herein, we showed by immunofluorescence and electron microscopy that in xenotransplanted mice, leukaemic cells infiltrate the connective tissue stroma of the choroid plexus, the brain structure responsible for the production of cerebrospinal fluid. The ultrastructural study also showed that leukaemia cells are able to migrate through blood vessels located in the choroid plexus stroma. In short-term co-cultures, leukaemic cells established strong interactions with human choroid plexus fibroblasts, mediated by an increased expression of ITGA4 (VLA-4)/ITGAL (LFA-1) and their ligands VCAM1/ICAM1. Upon contact with leukaemia cells, human choroid plexus fibroblasts acquired a cancer-associated fibroblast phenotype, with an increased expression of α-SMA and vimentin as well as pro-inflammatory factors. Human choroid plexus fibroblasts also have the capacity to reduce the proliferative index of leukaemic blasts and promote their survival and chemoresistance to methotrexate and cytarabine. The inhibition of VLA-4/VCAM-1 interactions using anti-VLA-4 antibodies, and the blockade of Notch signalling pathway by using a γ-secretase inhibitor partially restored chemotherapy sensitivity of leukaemia cells. We propose that the choroid plexus stroma constitutes a sanctuary for B-cell precursor acute lymphoblastic leukaemia cells in the central nervous system. © 2020 The Authors. The Journal of Pathology published by John Wiley & Sons, Ltd. on behalf of The Pathological Society of Great Britain and Ireland.

摘要

尽管目前有针对儿童 B 细胞前体急性淋巴细胞白血病的中枢神经系统导向治疗方法,但该解剖部位的复发仍然是一个具有挑战性的问题。很少有报道涉及研究特定的细胞微环境,这些微环境可以促进 B 细胞前体急性淋巴细胞白血病细胞在中枢神经系统中的存活、静止和因此产生的耐药性。在这里,我们通过免疫荧光和电子显微镜显示,在异种移植小鼠中,白血病细胞浸润脉络丛的结缔组织基质,脉络丛是负责产生脑脊液的脑结构。超微结构研究还表明,白血病细胞能够穿过位于脉络丛基质中的血管。在短期共培养中,白血病细胞与人脉络丛成纤维细胞建立了强烈的相互作用,这是通过 ITGA4(VLA-4)/ITGAL(LFA-1)及其配体 VCAM1/ICAM1 的表达增加介导的。与人脉络丛成纤维细胞接触后,获得了癌症相关成纤维细胞表型,α-SMA 和波形蛋白以及促炎因子的表达增加。人脉络丛成纤维细胞还具有降低白血病母细胞增殖指数并促进其存活和对甲氨蝶呤和阿糖胞苷的耐药性的能力。使用抗 VLA-4 抗体抑制 VLA-4/VCAM-1 相互作用,以及使用 γ-分泌酶抑制剂阻断 Notch 信号通路部分恢复了白血病细胞的化疗敏感性。我们提出脉络丛基质构成了中枢神经系统中 B 细胞前体急性淋巴细胞白血病细胞的避难所。© 2020 作者。《病理学杂志》由 John Wiley & Sons,Ltd. 代表英国和爱尔兰病理学学会出版。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2409/7540040/b7ba6d5ad28d/PATH-252-189-g001.jpg

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