Laboratory of Cell Biology, National Cancer Institute, National Institutes of Health, Bethesda, MD, USA.
Biomaterials. 2013 Nov;34(33):8301-13. doi: 10.1016/j.biomaterials.2013.07.013. Epub 2013 Jul 30.
Modeling tumor growth in vitro is essential for cost-effective testing of hypotheses in preclinical cancer research. 3-D cell culture offers an improvement over monolayer culture for studying cellular processes in cancer biology because of the preservation of cell-cell and cell-ECM interactions. Oxygen transport poses a major barrier to mimicking in vivo environments and is not replicated in conventional cell culture systems. We hypothesized that we can better mimic the tumor microenvironment using a bioreactor system for controlling gas exchange in cancer cell cultures with silicone hydrogel synthetic vessels. Soft-lithography techniques were used to fabricate oxygen-permeable silicone hydrogel membranes containing arrays of micropillars. These membranes were inserted into a bioreactor and surrounded by basement membrane extract (BME) within which fluorescent ovarian cancer (OVCAR8) cells were cultured. Cell clusters oxygenated by synthetic vessels showed a ∼100μm drop-off to anoxia, consistent with in vivo studies of tumor nodules fed by the microvasculature. Oxygen transport in the bioreactor system was characterized by experimental testing with a dissolved oxygen probe and finite element modeling of convective flow. Our study demonstrates differing growth patterns associated with controlling gas distributions to better mimic in vivo conditions.
在体外模拟肿瘤生长对于临床前癌症研究中检验假设至关重要。3D 细胞培养为研究癌症生物学中的细胞过程提供了优于单层培养的方法,因为它保留了细胞-细胞和细胞-ECM 的相互作用。氧气传输是模拟体内环境的主要障碍,在传统的细胞培养系统中无法复制。我们假设,我们可以使用生物反应器系统更好地模拟肿瘤微环境,该系统用于控制含有硅酮水凝胶合成容器的癌细胞培养物中的气体交换。软光刻技术用于制造含有微柱阵列的透气硅酮水凝胶膜。这些膜被插入生物反应器中,并被基底膜提取物 (BME) 包围,荧光卵巢癌细胞 (OVCAR8) 在其中培养。由合成容器增氧的细胞簇的缺氧区下降约 100μm,与微脉管滋养的肿瘤结节的体内研究一致。通过溶解氧探头的实验测试和对对流流的有限元建模对生物反应器系统中的氧气传输进行了表征。我们的研究表明,控制气体分布与更好地模拟体内条件相关联的不同生长模式。