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在斑马鱼异种移植模型中体内监测白血病龛位相互作用。

In vivo monitoring of leukemia-niche interactions in a zebrafish xenograft model.

机构信息

Department of Pediatric Hematology/Oncology, Dr. von Hauner Children's Hospital, Ludwig Maximilians University (LMU), Munich, Germany.

Institute of Epigenetics and Stem Cells, Helmholtz Centre Munich, German Research Center for Environmental Health, Munich, Germany.

出版信息

PLoS One. 2024 Aug 30;19(8):e0309415. doi: 10.1371/journal.pone.0309415. eCollection 2024.

Abstract

Acute lymphoblastic leukemia (ALL) is the most common type of malignancy in children. ALL prognosis after initial diagnosis is generally good; however, patients suffering from relapse have a poor outcome. The tumor microenvironment is recognized as an important contributor to relapse, yet the cell-cell interactions involved are complex and difficult to study in traditional experimental models. In the present study, we established an innovative larval zebrafish xenotransplantation model, that allows the analysis of leukemic cells (LCs) within an orthotopic niche using time-lapse microscopic and flow cytometric approaches. LCs homed, engrafted and proliferated within the hematopoietic niche at the time of transplant, the caudal hematopoietic tissue (CHT). A specific dissemination pattern of LCs within the CHT was recorded, as they extravasated over time and formed clusters close to the dorsal aorta. Interactions of LCs with macrophages and endothelial cells could be quantitatively characterized. This zebrafish model will allow the quantitative analysis of LCs in a functional and complex microenvironment, to study mechanisms of niche mediated leukemogenesis, leukemia maintenance and relapse development.

摘要

急性淋巴细胞白血病(ALL)是儿童中最常见的恶性肿瘤类型。ALL 患者在初始诊断后的预后通常较好;然而,复发的患者预后较差。肿瘤微环境被认为是复发的重要因素,但涉及的细胞-细胞相互作用复杂,难以在传统的实验模型中进行研究。在本研究中,我们建立了一种创新的幼虫斑马鱼异种移植模型,该模型允许使用延时显微镜和流式细胞术分析原位造血龛中的白血病细胞(LC)。LC 在移植时归巢、植入并在造血龛(尾造血组织,CHT)中增殖。记录了 LCs 在 CHT 内特定的扩散模式,因为它们随着时间的推移渗出并在靠近背主动脉的地方形成簇。LC 与巨噬细胞和内皮细胞的相互作用可以进行定量描述。这种斑马鱼模型将允许在功能和复杂的微环境中定量分析 LCs,以研究龛介导的白血病发生、白血病维持和复发发展的机制。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/19a6/11364250/f3d8249c5660/pone.0309415.g001.jpg

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