Interferon-delta:: The first member of a novel type I interferon family

被引:80
作者
Lefèvre, F
Guillomot, M
D'Andréa, S
Battegay, S
La Bonnardière, C
机构
[1] INRA, Unite Virol & Immunol Mol, F-78352 Jouy En Josas, France
[2] INRA, Unite Biol Cellulaire & Mol, F-78352 Jouy En Josas, France
关键词
type I interferon; trophoblast; pig; interferon-delta; gestation;
D O I
10.1016/S0300-9084(99)80030-3
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
We have recently described a novel type I interferon (IFN) co-expressed with IFN-gamma by the trophectoderm of the pig conceptus between day 12 and day 18 of gestation, a development stage that corresponds to implantation in the uterus. This IFN, now officially named IFN-delta, is recognized as the first member of a novel type I IFN family. This paper reviews the main published data on IFN-delta, together with some new data, showing that IFN-delta, while being a true type I IFN, has some very specific structural and biological properties. Sequences related to IFN-delta coding sequence were found in the genome of man and other ungulates but the only other potentially functional gene was found, so far, in the horse. The pig IFN-delta mature protein, with 149 amino acids, is the smallest of all known type I IFNs. It is unusually rich in cysteines (seven residues), and has a very basic isoelectric point. Recombinant IFN-delta expressed in insect cells is glycosylated and has a high antiviral activity on porcine cells, but not on human cells. It has high antiproliferative activity, which is significantly enhanced in the presence of IFN-gamma. This new IFN was shown to bind on pig cells to the sane type I receptor as IFN-alpha. IFN-delta and IFN-gamma genes are co-regulated in the pig trophectoderm, whose cells on day 14-16 of development simultaneously secrete both IFN proteins. The biological role of porcine IFN-delta in early pregnancy has been found unrelated to the known antiluteolytic effect of trophoblastic IFN-tau in ruminants. (C) Societe francaise de biochimie et biologie moleculaire/Elsevier, Paris.
引用
收藏
页码:779 / 788
页数:10
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