BioMedical Systems Engineering Laboratory, Wallace H. Coulter Department of Biomedical Engineering, The Georgia Institute of Technology, Atlanta, GA.
School of Pharmacy and Pharmaceutical Sciences, Trinity Translational Medicine Institute, Trinity College Dublin, Dublin, Ireland.
J Immunol. 2023 Apr 1;210(7):895-904. doi: 10.4049/jimmunol.2200836.
Hematoimmunopoiesis takes place in the adult human bone marrow (BM), which is composed of heterogeneous niches with complex architecture that enables tight regulation of homeostatic and stress responses. There is a paucity of representative culture systems that recapitulate the heterogeneous three-dimensional (3D) human BM microenvironment and that can endogenously produce soluble factors and extracellular matrix that deliver culture fidelity for the study of both normal and abnormal hematopoiesis. Native BM lymphoid populations are also poorly represented in current in vitro and in vivo models, creating challenges for the study and treatment of BM immunopathology. BM organoid models leverage normal 3D organ structure to recreate functional niche microenvironments. Our focus herein is to review the current state of the art in the use of 3D BM organoids, focusing on their capacities to recreate critical quality attributes of the in vivo BM microenvironment for the study of human normal and abnormal hematopoiesis.
人骨髓(BM)中的造血免疫发生,它由具有复杂结构的异质龛组成,使稳态和应激反应得到严格调控。目前缺乏能够重现异质三维(3D)人 BM 微环境并能够内源性产生可溶性因子和细胞外基质的代表性培养系统,这为正常和异常造血的研究提供了培养保真度。目前的体外和体内模型也不能很好地代表天然 BM 淋巴细胞群,这给 BM 免疫病理学的研究和治疗带来了挑战。BM 类器官模型利用正常的 3D 器官结构来重现功能性龛微环境。我们在此重点回顾 3D BM 类器官应用的最新技术进展,重点关注它们在研究人类正常和异常造血时重现体内 BM 微环境关键质量属性的能力。