Parikh Mukti R, Belch Andrew R, Pilarski Linda M, Kirshner Julia
Department of Biological Sciences, Purdue University.
Department of Oncology, University of Alberta; Cross Cancer Institute.
J Vis Exp. 2014 Mar 8(85):50947. doi: 10.3791/50947.
Tissue culture has been an invaluable tool to study many aspects of cell function, from normal development to disease. Conventional cell culture methods rely on the ability of cells either to attach to a solid substratum of a tissue culture dish or to grow in suspension in liquid medium. Multiple immortal cell lines have been created and grown using such approaches, however, these methods frequently fail when primary cells need to be grown ex vivo. Such failure has been attributed to the absence of the appropriate extracellular matrix components of the tissue microenvironment from the standard systems where tissue culture plastic is used as a surface for cell growth. Extracellular matrix is an integral component of the tissue microenvironment and its presence is crucial for the maintenance of physiological functions such as cell polarization, survival, and proliferation. Here we present a 3-dimensional tissue culture method where primary bone marrow cells are grown in extracellular matrix formulated to recapitulate the microenvironment of the human bone (rBM system). Embedded in the extracellular matrix, cells are supplied with nutrients through the medium supplemented with human plasma, thus providing a comprehensive system where cell survival and proliferation can be sustained for up to 30 days while maintaining the cellular composition of the primary tissue. Using the rBM system we have successfully grown primary bone marrow cells from normal donors and patients with amyloidosis, and various hematological malignancies. The rBM system allows for direct, in-matrix real time visualization of the cell behavior and evaluation of preclinical efficacy of novel therapeutics. Moreover, cells can be isolated from the rBM and subsequently used for in vivo transplantation, cell sorting, flow cytometry, and nucleic acid and protein analysis. Taken together, the rBM method provides a reliable system for the growth of primary bone marrow cells under physiological conditions.
组织培养一直是研究细胞功能诸多方面的宝贵工具,涵盖从正常发育到疾病的各个领域。传统的细胞培养方法依赖于细胞附着在组织培养皿的固体基质上或在液体培养基中悬浮生长的能力。利用这些方法已经创建并培养了多种永生细胞系,然而,当需要在体外培养原代细胞时,这些方法常常失效。这种失效被归因于标准系统中缺乏组织微环境中合适的细胞外基质成分,在这些标准系统中,组织培养塑料被用作细胞生长的表面。细胞外基质是组织微环境的一个组成部分,其存在对于维持诸如细胞极化、存活和增殖等生理功能至关重要。在此,我们介绍一种三维组织培养方法,其中原代骨髓细胞在模拟人骨微环境的细胞外基质中生长(rBM系统)。细胞嵌入细胞外基质中,通过添加人血浆的培养基获得营养,从而提供了一个全面的系统,在该系统中细胞存活和增殖可持续长达30天,同时保持原代组织的细胞组成。使用rBM系统,我们成功地培养了来自正常供体以及淀粉样变性和各种血液系统恶性肿瘤患者的原代骨髓细胞。rBM系统允许对细胞行为进行直接的基质内实时可视化,并评估新型治疗方法的临床前疗效。此外,细胞可以从rBM中分离出来,随后用于体内移植、细胞分选、流式细胞术以及核酸和蛋白质分析。综上所述,rBM方法为在生理条件下培养原代骨髓细胞提供了一个可靠的系统。