Technische Hochschule Darmstadt, Inst. f. Biochemie, Petersenstr. 22, D-64287, Darmstadt, Germany.
Cytotechnology. 1998 Jan;26(1):49-58. doi: 10.1023/A:1007989802251.
An alternative culture system has been developed based on a conventional tissue culture plate (3.5 cm diameter) which is changed into a closed perfusion chamber. The system can easily be scaled up from one to several chambers. The shape and the size of the area of cell growth may be designed to individual experimental demands. The whole culture chamber is optically accessible, so cell growth and morphology can be evaluated by light microscopy. Furthermore the cellular physiology can be characterised by any fluorimetric assay using a bottom type fluorescence reader. A peristaltic pump sustains a constant medium flow through the chamber thus creating true homeostasis. The use of HPLC-valves and connectors allows the switching between different media or assay solutions. Thus it is possible to perform in situ assays also measuring transient effects. A protocol for vitality tests using calcein-AM is worked out for an adherent cell line and for a suspension cell line. The lower detection limits are 7 × 10(2) cells cm(-2) for the adherent cells and 5 × 10(4) cells mL(-1) for the suspension cells. The upper limits are 1-2 × 10(5) cells cm(-2) respectively 8 × 10(6) cells mL(-1).
已经开发了一种替代的基于常规组织培养板(3.5cm 直径)的培养系统,该培养板被改造成一个封闭的灌注室。该系统可以很容易地从一个腔室扩展到多个腔室。细胞生长区域的形状和大小可以根据实验需求进行设计。整个培养腔室具有光学通透性,因此可以通过光学显微镜评估细胞生长和形态。此外,通过使用底部荧光读取器进行任何荧光分析,都可以对细胞生理学进行表征。蠕动泵维持通过腔室的恒定培养基流,从而实现真正的动态平衡。使用 HPLC 阀和连接器可以在不同的培养基或分析溶液之间进行切换。因此,可以进行原位测定,也可以测量瞬时效应。为贴壁细胞系和悬浮细胞系制定了使用 calcein-AM 进行活力测试的方案。对于贴壁细胞,检测下限为 7×10(2)细胞/cm(-2),对于悬浮细胞,检测下限为 5×10(4)细胞/mL(-1)。上限分别为 1-2×10(5)细胞/cm(-2)和 8×10(6)细胞/mL(-1)。