{"title":"An immunocompetent bone marrow-on-a-chip model for studying human hematological malignancies and preclinical therapeutic screening.","authors":"Huishu Wang, Lunan Liu, Weiqiang Chen","doi":"10.1038/s41596-026-01387-1","DOIUrl":null,"url":null,"abstract":"<p><p>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.</p>","PeriodicalId":18901,"journal":{"name":"Nature Protocols","volume":" ","pages":""},"PeriodicalIF":18.4000,"publicationDate":"2026-06-11","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Nature Protocols","FirstCategoryId":"99","ListUrlMain":"https://doi.org/10.1038/s41596-026-01387-1","RegionNum":1,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"BIOCHEMICAL RESEARCH METHODS","Score":null,"Total":0}
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.
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.