Department of Molecular Genetics, Weizmann Institute of Science, 76 100, Rehovot, Israel.
Cytotechnology. 2001 Oct;37(2):75-81. doi: 10.1023/A:1019914630465.
We describe a carrier with some unusual properties."Cellrafts" increase yields from adherent cells in conventional static T150 flasks, by floating multilayer strips of transparent film at the oxygen-rich surface of unstirred medium. This new technique allowed microscopic inspection of cell growth inside the carriers during bulk culture. Individual carriers could be picked out for subculture of selected colonies. A novel surface treatment by hypochlorite/uv allowed recycling of used carriers. Cellrafts' open-deck structure facilitated trypsinization with90% release as viable single cells from bulk carriers. Macro size (10mm by 1 mm) enables retention in flask by a coarse sieve insert in its neck, facilitating separation of product cells or media. Residual cells in carriers regenerated repeated harvests without need for reseeding. Carriers were tested with shear-sensitive CHO clones expressing soluble human IL6 receptor (sIL6R). Control was monolayer bulk culture on trays. Floating multilayer cultures remained viable longer than monolayers, had higher cellular activity of protein expression, and were less serum dependent (resembling cells on porous carriers). Purity and anti-sIL6R binding were identical to control product. Cellrafts were also tested in a small spinner vessel, but for litre batches this proved less convenient than in T-flasks. Though yields are low compared to well established porous carrier technology (spinner or packed bed) static transparent carriers might provide transitional scaleup from normal cytogenetics laboratory culture.
我们描述了一种具有一些特殊性质的载体。“细胞筏”通过在未搅拌的培养基的富氧表面上漂浮多层透明薄膜,增加了常规静态 T150 瓶中贴壁细胞的产量。这项新技术允许在大规模培养过程中对载体内部的细胞生长进行微观检查。可以挑选出单个载体用于选择的菌落的亚培养。通过次氯酸盐/紫外线的新型表面处理允许重复使用用过的载体。细胞筏的开放式甲板结构便于用胰蛋白酶从大块载体中以 90%的存活率释放为活的单细胞。宏观尺寸(10mm 乘 1mm)使其可以通过颈部的粗筛插入物保留在瓶中,便于分离产物细胞或培养基。载体中残留的细胞无需重新接种即可再生多次收获。载体用表达可溶性人白细胞介素 6 受体 (sIL6R) 的剪切敏感 CHO 克隆进行了测试。对照是在托盘上的单层大规模培养。多层漂浮培养比单层培养更具活力,细胞表达蛋白的活性更高,对血清的依赖性更低(类似于多孔载体上的细胞)。纯度和抗 sIL6R 结合与对照产物相同。细胞筏也在小型搅拌器容器中进行了测试,但对于升批次,这比在 T 瓶中更不方便。尽管与成熟的多孔载体技术(搅拌或填充床)相比产量较低,但静态透明载体可能为从正常细胞遗传学实验室培养过渡到大规模生产提供了途径。