4.6 Article

Knockout of caspase-7 gene improves the expression of recombinant protein in CHO cell line through the cell cycle arrest in G2/M phase

Journal

BIOLOGICAL RESEARCH
Volume 55, Issue 1, Pages -

Publisher

SOC BIOLGIA CHILE
DOI: 10.1186/s40659-021-00369-9

Keywords

Caspase-7; Caspase-3; CRISPR; Cas9; Recombinant protein; Cell cycle; Chinese hamster ovary cell line

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Funding

  1. Diagnostic Laboratory Sciences and Technology Research Center, School of Paramedical Sciences, Shiraz University of Medical Sciences, Shiraz, Iran

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This study assessed the effect of caspase-7 deficiency on CHO cell growth, viability, and protein expression. The findings showed that the absence of caspase-7 decreased cell growth and viability, but resulted in enhanced recombinant protein expression due to cell cycle arrest. Additionally, caspase-3 enzymatic activity increased in the absence of caspase-7 in apoptotic situations.
Background Chinese hamster ovary cell line has been used routinely as a bioproduction factory of numerous biopharmaceuticals. So far, various engineering strategies have been recruited to improve the production efficiency of this cell line such as apoptosis engineering. Previously, it is reported that the caspase-7 deficiency in CHO cells reduces the cell proliferation rate. But the effect of this reduction on the CHO cell productivity remained unclear. Hence, in the study at hand the effect of caspase-7 deficiency was assessed on the cell growth, viability and protein expression. In addition, the enzymatic activity of caspase-3 was investigated in the absence of caspase-7. Results Findings showed that in the absence of caspase-7, both cell growth and cell viability were decreased. Cell cycle analysis illustrated that the CHO knockout (CHO-KO) cells experienced a cell cycle arrest in G2/M phase. This cell cycle arrest resulted in a 1.7-fold increase in the expression of luciferase in CHO-KO cells compared to parenteral cells. Furthermore, in the apoptotic situation the enzymatic activity of caspase-3 in CHO-KO cells was approximately 3 times more than CHO-K1 cells. Conclusions These findings represented that; however, caspase-7 deficiency reduces the cell proliferation rate but the resulted cell cycle arrest leads to the enhancement of recombinant protein expression. Moreover, increasing in the caspase-3 enzymatic activity compensates the absence of caspase-7 in the caspase cascade of apoptosis.

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