Laboratório de Imunologia Viral, Instituto Butantan, São Paulo, Brazil.
Appl Biochem Biotechnol. 2011 Jun;164(4):401-9. doi: 10.1007/s12010-010-9143-5. Epub 2010 Dec 23.
Since the recombinant thyroid-stimulating hormone (rhTSH) is secreted by stably transfected Chinese hamster ovary (CHO-hTSH) cells, a bioprocess consisting of immobilizing the cells on a substrate allowing their multiplication is very suitable for rhTSH recovering from supernatants at relative high degree of purity. In addition, such a system has also the advantage of easily allowing delicate manipulations of culture medium replacement. In the present study, we show the development of a laboratory scale bioprocess protocol of CHO-hTSH cell cultures on cytodex microcarriers (MCs) in a 1 L bioreactor, for the preparation of rhTSH batches in view of structure/function studies. CHO-hTSH cells were cultivated on a fetal bovine serum supplemented medium during cell growth phase. For rhTSH synthesis phase, 75% of supernatant was replaced by animal protein-free medium every 24 h. Cell cultures were monitored for agitation (rpm), temperature (°C), dissolved oxygen (% DO), pH, cell concentration, MCs coverage, glucose consumption, lactate production, and rhTSH expression. The results indicate that the amount of MCs in the culture and the cell concentration at the beginning of rhTSH synthesis phase were crucial parameters for improving the final rhTSH production. By cultivating the CHO-hTSH cells with an initial cell seeding of four cells/MC on 4 g/L of MCs with a repeated fed batch mode of operation at 40 rpm, 37 °C, 20% DO, and pH 7.2 and starting the rhTSH synthesis phase with 3 × 10(6) cells/mL, we were able to supply the cultures with enough glucose, to maintain low levels of lactate, and to provide high percent (∼80%) of fully covered MCs for a long period (5 days) and attain a high cell concentration (∼9 × 10(5) cells/mL). The novelty of the present study is represented by the establishment of cell culture conditions allowing us to produce ∼1.6 mg/L of rhTSH in an already suitable degree of purity. Batches of produced rhTSH were purified and showed biological activity.
由于重组促甲状腺素(rhTSH)是由稳定转染的中国仓鼠卵巢(CHO-hTSH)细胞分泌的,因此包含将细胞固定在允许其增殖的基质上的生物过程非常适合从相对高纯度的上清液中回收 rhTSH。此外,这种系统还具有易于进行培养基更换等精细操作的优点。在本研究中,我们展示了在 1L 生物反应器中使用微载体(MCs)培养 CHO-hTSH 细胞的实验室规模生物过程方案的开发,目的是制备用于结构/功能研究的 rhTSH 批次。CHO-hTSH 细胞在含有胎牛血清的培养基中进行细胞生长阶段的培养。在 rhTSH 合成阶段,每 24 小时用无动物蛋白的培养基替换 75%的上清液。监测细胞培养物的搅拌速度(rpm)、温度(°C)、溶解氧(% DO)、pH 值、细胞浓度、MC 覆盖率、葡萄糖消耗、乳酸生成和 rhTSH 表达情况。结果表明,培养物中 MC 的数量和 rhTSH 合成阶段开始时的细胞浓度是提高最终 rhTSH 产量的关键参数。通过以 40rpm 的转速、37°C、20% DO 和 pH7.2 的条件,用 4g/L 的 MC 以重复分批操作的方式初始接种四个细胞/MC,并且在以 3×10(6)个细胞/mL 的细胞浓度开始 rhTSH 合成阶段,我们能够为培养物提供足够的葡萄糖,维持低水平的乳酸,并为高比例(约 80%)的完全覆盖的 MC 提供长时间(5 天),并获得高细胞浓度(约 9×10(5)个细胞/mL)。本研究的新颖之处在于建立了细胞培养条件,使我们能够以已经相当高的纯度生产约 1.6mg/L 的 rhTSH。生产的 rhTSH 批次经过纯化并显示出生物活性。