USE OF REGULATED SECRETION IN PROTEIN-PRODUCTION FROM ANIMAL-CELLS - AN EVALUATION WITH THE ATT-20 MODEL CELL-LINE

被引:18
作者
SAMBANIS, A
STEPHANOPOULOS, G
SINSKEY, AJ
LODISH, HF
机构
[1] MIT, DEPT CHEM ENGN, CAMBRIDGE, MA 02139 USA
[2] MIT, CTR BIOTECHNOL PROC ENGN, CAMBRIDGE, MA 02139 USA
[3] MIT, DEPT BIOL, CAMBRIDGE, MA 02139 USA
[4] WHITEHEAD INST BIOMED RES, CAMBRIDGE, MA 02142 USA
关键词
D O I
10.1002/bit.260350804
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Regulated secretion, i.e., the ability of certain specialized animal cells to store secretory proteins intracellularly and release them upon stimulation, may be used to realize production schemes that facilitate downstream processing of protein products. Mouse AtT‐20 cells expressing recombinant human insulin and human growth hormone (hGH) were found to secrete the proteins at relatively low and constant rates when exposed to media with no secretion agonists: basal rates were 1.0–1.6 μU insulin‐reiated peptides and 0.38 ng hGH/105 cells‐h. When induced with 8 brorno‐cyclic AMP (BrcAMP), the cells secreted recombinant proteins at initial rates 3.5–9‐fold higher. A cycling secretion experiment was conducted with the insulin‐producing cells in which the cells were exposed alternately to complete growth medium and to secretion medium with BrcAMP. During the first three cycles, the cells secreted immunoreactive insulin at the foregoing high induced rates when they were exposed to BrcAMP. The cells then started to detach from the culture surface, leading to a reduction of BrcAMP‐induced secretion. Operational modifications that may result in improved system performance are discussed. Copyright © 1990 John Wiley & Sons, Inc.
引用
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页码:771 / 780
页数:10
相关论文
共 19 条
[1]  
BARNES D, 1987, BIOTECHNIQUES, V5, P534
[2]   THE EXOCRINE PROTEIN TRYPSINOGEN IS TARGETED INTO THE SECRETORY GRANULES OF AN ENDOCRINE CELL-LINE - STUDIES BY GENE-TRANSFER [J].
BURGESS, TL ;
CRAIK, CS ;
KELLY, RB .
JOURNAL OF CELL BIOLOGY, 1985, 101 (02) :639-645
[3]  
CHANCE RE, 1981, PEPTIDES SYNTHESIS S
[4]   MOLECULAR SORTING IN THE SECRETORY PATHWAY [J].
CHUNG, KN ;
WALTER, P ;
APONTE, GW ;
MOORE, HPH .
SCIENCE, 1989, 243 (4888) :192-197
[5]  
Darnell J., 1986, MOL CELL BIOL
[6]   BETA-CELL LINES DERIVED FROM TRANSGENIC MICE EXPRESSING A HYBRID INSULIN GENE ONCOGENE [J].
EFRAT, S ;
LINDE, S ;
KOFOD, H ;
SPECTOR, D ;
DELANNOY, M ;
GRANT, S ;
HANAHAN, D ;
BAEKKESKOV, S .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1988, 85 (23) :9037-9041
[7]   LARGE-SCALE PRODUCTION OF MAMMALIAN-CELLS AND THEIR PRODUCTS - ENGINEERING PRINCIPLES AND BARRIERS TO SCALE-UP [J].
GLACKEN, MW ;
FLEISCHAKER, RJ ;
SINSKEY, AJ .
ANNALS OF THE NEW YORK ACADEMY OF SCIENCES, 1983, 413 (DEC) :355-372
[8]   2 DISTINCT INTRACELLULAR PATHWAYS TRANSPORT SECRETORY AND MEMBRANE-GLYCOPROTEINS TO THE SURFACE OF PITUITARY-TUMOR CELLS [J].
GUMBINER, B ;
KELLY, RB .
CELL, 1982, 28 (01) :51-59
[9]  
HOPCROFT DW, 1985, IN VITRO CELL DEV B, V21, P421
[10]   PATHWAYS OF PROTEIN SECRETION IN EUKARYOTES [J].
KELLY, RB .
SCIENCE, 1985, 230 (4721) :25-32