Department of Cancer Biology, Vanderbilt University Medical Center, Nashville, TN 37232, USA.
Lab Chip. 2012 Nov 7;12(21):4560-8. doi: 10.1039/c2lc40304h.
We have developed a novel, portable, gravity-fed, microfluidics-based platform suitable for optical interrogation of long-term organotypic cell culture. This system is designed to provide convenient control of cell maintenance, nutrients, and experimental reagent delivery to tissue-like cell densities housed in a transparent, low-volume microenvironment. To demonstrate the ability of our Thick-Tissue Bioreactor (TTB) to provide stable, long-term maintenance of high-density cellular arrays, we observed the morphogenic growth of human mammary epithelial cell lines, MCF-10A and their invasive variants, cultured under three-dimensional (3D) conditions inside our system. Over the course of 21 days, these cells typically develop into hollow "mammospheres" if cultured in standard 3D Matrigel. This complex morphogenic process requires alterations in a variety of cellular functions, including degradation of extracellular matrix that is regulated by cell-produced matrix proteinases. For our "drug" delivery testing and validation experiments we have introduced proteinase inhibitors into the fluid supply system, and we observed both reduced proteinase activity and inhibited cellular morphogenesis. The size inhibition results correlated well with the overall proteinase activities of the tested cells.
我们开发了一种新颖的、便携式的、重力驱动的、基于微流控的平台,适用于对长期器官型细胞培养进行光学检测。该系统旨在方便地控制细胞维持、营养物质和实验试剂输送到类似组织的细胞密度中,这些细胞被安置在透明、低容量的微环境中。为了证明我们的厚组织生物反应器(TTB)能够稳定地长期维持高密度细胞阵列,我们观察了在我们的系统内三维(3D)条件下培养的人乳腺上皮细胞系 MCF-10A 及其侵袭变体的形态发生生长。在 21 天的过程中,如果在标准的 3D Matrigel 中培养,这些细胞通常会发展成空心的“乳腺球体”。这个复杂的形态发生过程需要改变各种细胞功能,包括细胞产生的基质蛋白酶调节的细胞外基质的降解。对于我们的“药物”输送测试和验证实验,我们已经将蛋白酶抑制剂引入到流体供应系统中,并且我们观察到了蛋白酶活性的降低和细胞形态发生的抑制。尺寸抑制结果与所测试细胞的整体蛋白酶活性很好地相关。