Response of recombinant Chinese hamster ovary cells to hyperosmotic pressure: effect of Bcl-2 overexpression
- 作者：Kim ; No Soo ; Lee ; Gyun Min
- 关键词：Antibody ; Apoptosis ; Bcl-2 overexpression ; Chinese hamster ovary (CHO) cells ; Hyperosmotic pressure
- 刊名：Journal of Biotechnology
- 出版年：2002
- 期刊代码：53_01681656
- 类别：imm
- 出版时间：May 23, 2002
- 卷：95
- 期：3
- 页码：237-248
- 文件大小：267 K
摘要
In an attempt to use the hyperosmotic pressure for improved foreign protein production in recombinant Chinese hamster ovary (rCHO) cells, the response of rCHO cells producing a humanized antibody (SH2-0.32-Δbcl-2 cells) to hyperosmotic pressure was determined in regard to cell growth and death, and antibody production. Further, the feasibility of Bcl-2 overexpression in improving rCHO cell viability under hyperosmotic pressure was also determined by comparing control cells (SH2-0.32-Δbcl-2) with Bcl-2 overexpressing cells (14C6-bcl-2). After 3 days of cultivation in the standard medium (294 mOsm kg−1), the spent medium was exchanged with the fresh media with various osmolalities (294–640 mOsm kg−1). The results obtained show that hyperosmotic pressure inhibited cell growth in a dose-dependent manner, though 14C6-bcl-2 cells were less susceptible to hyperosmotic pressure than SH2-0.32-Δbcl-2 cells. At 522 mOsm kg−1, SH2-0.32-Δbcl-2 cells underwent a gradual cell death mainly through apoptosis due to the cytotoxic effect of hyperosmotic pressure. In contrast, Bcl-2 overexpression in 14C6-bcl-2 cells could delay the apoptosis induced by 522 mOsm kg−1 by inhibiting caspase-3 activation. Bcl-2 overexpression could also improve the cellular membrane integrity of 14C6-bcl-2 cells. When subjected to hyperosmotic pressure, the specific antibody productivity of SH2-0.32-Δbcl-2 cells and 14C6-bcl-2 cells was increased in a similar extent. As a result, the final antibody concentration achieved in 14C6-bcl-2 cells at 522 mOsm kg−1 was 2.5-fold higher than that at 294 mOsm kg−1. At 580 mOsm kg−1, acute hyperosmotic pressure induced the rapid loss of viability in both SH2-0.32-Δbcl-2 and 14C6-bcl-2 cells through necrosis rather than through apoptosis. Taken together, Bcl-2 overexpression and optimized hyperosmotic pressure could improve the antibody production of rCHO cells.