SECRETORY PRODUCTION OF BIOACTIVE RECOMBINANT HUMAN GRANULOCYTE-MACROPHAGE COLONY-STIMULATING FACTOR BY A BACULOVIRUS EXPRESSION SYSTEM

Citation
Lc. Au et al., SECRETORY PRODUCTION OF BIOACTIVE RECOMBINANT HUMAN GRANULOCYTE-MACROPHAGE COLONY-STIMULATING FACTOR BY A BACULOVIRUS EXPRESSION SYSTEM, Journal of biotechnology, 51(2), 1996, pp. 107-113
Citations number
19
Categorie Soggetti
Biothechnology & Applied Migrobiology
Journal title
ISSN journal
01681656
Volume
51
Issue
2
Year of publication
1996
Pages
107 - 113
Database
ISI
SICI code
0168-1656(1996)51:2<107:SPOBRH>2.0.ZU;2-G
Abstract
The proliferation and differentiation of hematopoietic cells are stimu lated by a group of glycoproteins called colony stimulating factors (C SFs). Previously, we found that the human hepatoma cell line HA22T/VGH secreted a high level of human granulocyte-macrophage colony-stimulat ing factor (hGM-CSF). The cDNA of hGM-CSF, including the signal peptid e sequence, was amplified from the total RNA of HA22T/VGH by a reverse -transcription polymerase chain reaction and was cloned into the pUC18 vector. After confirming the nucleotide sequence, the cDNA was insert ed into a pVL1393 baculovirus transfer vector. The recombinant baculov irus carrying hGM-CSF cDNA was generated by co-transfecting the hGM-CS F recombinant transfer vector and BaculoGold(TM) baculovirus DNA into the Sf9 insect cells. The expected hGM-CSF transcript was detected in the recombinant virus-infected Sf9 cells. The conditioned media of the infected cells were analyzed by a slot-blot immunoassay. The results indicate that the infected insect cells produced and secreted hGM-CSF. According to colony forming assay, a maximum titer of 2.1 x 10(6) U m l(-1) of hGM-CSF in the medium was obtained on the third day after inf ection.