An immunocompetent bone marrow-on-a-chip model for studying human hematological malignancies and preclinical therapeutic screening.

IF 18.4 1区 生物学 Q1 BIOCHEMICAL RESEARCH METHODS
Huishu Wang, Lunan Liu, Weiqiang Chen
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引用次数: 0

Abstract

The complex pathophysiology of leukemia and other bone marrow-related hematological malignancies underscores the critical need for immunocompetent bone marrow models that can accurately recapitulate key disease microenvironment and patient therapeutic responses. Existing bone marrow models often lack the fidelity required to recapitulate patient-specific pathophysiology or to emulate the intricate dynamics of in vivo immune responses. This limitation ultimately constrains their utility in critical areas such as leukemia immunotherapy development. Here, to overcome this challenge, we present a detailed protocol for building a 3D microfluidic human bone marrow-on-a-chip microphysiological system that recapitulates the anatomical organization and function of the native tissue. Its concentric three-compartment design replicates the marrow's spatial architecture, co-culturing stromal and hematopoietic cells within a vascularized niche to establish a physiologically relevant, immunocompetent microenvironment. To model patient-specific biology, the platform incorporates patient-derived samples, enabling the personalized evaluation of therapeutic interventions such as chimeric antigen receptor T cell therapy and chemotherapy. The platform supports multiplexed readouts through live imaging, immunofluorescence, cytokine profiling, flow cytometry and single-cell sequencing, enabling a comprehensive analysis of treatment response. The protocol requires ~7 d to establish the functional bone marrow chip, comprising microfluidic device fabrication (1 d), cell seeding (1 d) and progressive development of the bone marrow model (5 d). Therapeutic testing is conducted over a variable timeframe, typically ranging from 2 d to 14 d. The protocol is designed for researchers with basic experience in cell culture and fluorescence imaging,who have basic microfluidics fabrication and tissue culture experience.

用于研究人类血液恶性肿瘤和临床前治疗筛选的免疫能力骨髓芯片模型。
白血病和其他骨髓相关的血液系统恶性肿瘤的复杂病理生理强调了对能够准确概括关键疾病微环境和患者治疗反应的免疫能力强的骨髓模型的迫切需要。现有的骨髓模型往往缺乏再现患者特异性病理生理或模拟体内免疫反应的复杂动力学所需的保真度。这一限制最终限制了它们在白血病免疫治疗发展等关键领域的应用。在这里,为了克服这一挑战,我们提出了一个详细的方案来构建一个3D微流体人骨髓芯片微生理系统,该系统概括了天然组织的解剖组织和功能。它的同心三室设计复制了骨髓的空间结构,在一个血管化的生态位内共同培养基质细胞和造血细胞,以建立一个生理相关的、具有免疫能力的微环境。为了模拟患者特异性生物学,该平台结合了患者来源的样本,使治疗干预措施(如嵌合抗原受体T细胞治疗和化疗)的个性化评估成为可能。该平台通过实时成像、免疫荧光、细胞因子分析、流式细胞术和单细胞测序支持多路读数,从而实现对治疗反应的全面分析。该方案需要约7天的时间来建立功能性骨髓芯片,包括微流体装置制造(1天),细胞播种(1天)和骨髓模型的逐步发展(5天)。治疗测试在一个可变的时间框架内进行,通常从2天到14天不等。该方案是为具有细胞培养和荧光成像基本经验的研究人员设计的,他们具有基本的微流体制造和组织培养经验。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Nature Protocols
Nature Protocols 生物-生化研究方法
CiteScore
29.10
自引率
0.70%
发文量
128
审稿时长
4 months
期刊介绍: Nature Protocols focuses on publishing protocols used to address significant biological and biomedical science research questions, including methods grounded in physics and chemistry with practical applications to biological problems. The journal caters to a primary audience of research scientists and, as such, exclusively publishes protocols with research applications. Protocols primarily aimed at influencing patient management and treatment decisions are not featured. The specific techniques covered encompass a wide range, including but not limited to: Biochemistry, Cell biology, Cell culture, Chemical modification, Computational biology, Developmental biology, Epigenomics, Genetic analysis, Genetic modification, Genomics, Imaging, Immunology, Isolation, purification, and separation, Lipidomics, Metabolomics, Microbiology, Model organisms, Nanotechnology, Neuroscience, Nucleic-acid-based molecular biology, Pharmacology, Plant biology, Protein analysis, Proteomics, Spectroscopy, Structural biology, Synthetic chemistry, Tissue culture, Toxicology, and Virology.
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