Secretion of biologically active human granulocyte colony-stimulating factor (G-CSF) in milk of transgenic mice

被引:3
|
作者
Dvoryanchikov, GA [1 ]
Serova, IA
Andreeva, LE
Dias, LPB
Azevedo, S
Serov, OL
机构
[1] Univ Fed Rio de Janeiro, Inst Biophys Carlos Chagas Filho, BR-21949900 Rio De Janeiro, Brazil
[2] Russian Acad Sci, Inst Cytol & Genet, Novosibirsk 630090, Russia
[3] Russian Acad Sci, Inst Mol Genet, Novosibirsk 630090, Russia
[4] Univ Fed Rio de Janeiro, Hosp Clemento Fraga Filho, Cellular Bank, BR-21949900 Rio De Janeiro, Brazil
关键词
D O I
10.1007/s11177-005-0204-8
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Two constructs were devised, containing the full-length gene of the human granulocyte colony-stimulating factor (G-CSF) fused with the 5' and 3' flanking promoter sequences of bovine alpha-S-1-casein gene (CSN1S1). Both constructs contained a 1518-bp fragment that included exons 18 and 19 and 320 bp of the 3' flanking region of bovine gene CSN1S1, but differed in size of the 5' flanking sequences, which were of 721 bp, and exon 1 in construct pGCm1 and 2001 bp and exon 1 and intron 1 in construct pGCm2. With both constructs, transgenic mice were produced. The transgene expression was assessed using RT-PCR and immunochemically from the production of human G-CSF in milk of lactating females. Secretion of human G-CSF into the milk varied in a wide range, from 0.8 mu g/ml to over 1 mg/ml, in mice with construct pGCm1 and was low (up to 60 mu g/ml) or absent in mice with construct pGCm2. G-CSF glycosylation was incomplete in mice with transgene pGCm1 and complete in mice with pGCm2. G-CSF of transgenic mouse milk was shown to stimulate the formation and growth of granulocyte-containing colonies in human umbilical blood cell culture and be close or identical in physiological activity to the natural human G-CSF.
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页码:1088 / 1094
页数:7
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