Joyce Margaret M, White Frankie J, Burghardt Robert C, Muñiz Jesus J, Spencer Thomas E, Bazer Fuller W, Johnson Greg A
Center for Animal Biotechnology and Genomics, Department of Veterinary Integrative Biosciences, Texas A&M University, College Station, Texas 77843-4458, USA.
Endocrinology. 2005 Feb;146(2):675-84. doi: 10.1210/en.2004-1224. Epub 2004 Nov 4.
Interferon-stimulated gene 15 (ISG15) is a ubiquitin homolog expressed in uteri of ruminants in response to interferon (IFN)-tau and is also induced during pregnancy in the uteri of mice, pigs, humans, and baboons. This study examined expression of ISG15 and its conjugation to target proteins in the ovine uterus beyond the period of IFNtau secretion by the conceptus. Although steady-state levels of ISG15 mRNA decreased after d 25 of pregnancy, ISG15 persisted in endometrium through d 120. In situ hybridization and immunocytochemistry localized ISG15 across the entire uterine wall through d 25, after which expression was restricted to endometrial stroma along the maternal-placental interface. Western blots revealed ISG15 and ISG15-conjugated proteins in endometrium. Treatment of ovariectomized sheep with progesterone and IFNtau increased both free and conjugated ISG15. These results are the first to show in vivo regulation of ISG15 function (i.e. conjugation to target proteins) by a type I IFN in the uterus of any species and that ISG15 is expressed at contacts between the placenta and uterus when trophectoderm no longer produces IFNtau. Interestingly, mRNA for the type II IFNgamma was present in the endometrial stromal compartment on d 15-50, which may stimulate the synthesis of ISG15 through later pregnancy. We hypothesize that ISG15 is not merely a consequence of an antiviral state induced by trophoblast IFNtau but represents a critical component of the microenvironment at the uterine-placental interface during the progressive events of conceptus development, implantation, and placentation in sheep and perhaps other mammalian species.
干扰素刺激基因15(ISG15)是一种泛素同源物,在反刍动物子宫中受干扰素(IFN)-τ刺激而表达,在小鼠、猪、人类和狒狒的子宫妊娠期间也会被诱导。本研究检测了在胚胎分泌IFN-τ的时期之后,ISG15在绵羊子宫中的表达及其与靶蛋白的缀合情况。尽管妊娠第25天后ISG15 mRNA的稳态水平下降,但ISG15在子宫内膜中持续存在至第120天。原位杂交和免疫细胞化学显示,直到第25天ISG15在整个子宫壁上均有表达,之后其表达局限于沿母胎胎盘界面的子宫内膜基质。蛋白质免疫印迹显示子宫内膜中有ISG15及其缀合蛋白。用孕酮和IFN-τ处理去卵巢绵羊会增加游离型和缀合型ISG15。这些结果首次表明,在任何物种的子宫中,I型干扰素可在体内调节ISG15的功能(即与靶蛋白的缀合),并且当滋养外胚层不再产生IFN-τ时,ISG15在胎盘与子宫的接触部位表达。有趣的是,在第15至50天,II型干扰素γ的mRNA存在于子宫内膜基质区室中,这可能在妊娠后期刺激ISG15的合成。我们推测,ISG15不仅仅是滋养层IFN-τ诱导的抗病毒状态的结果,而是绵羊以及可能其他哺乳动物物种在胚胎发育、着床和胎盘形成的渐进过程中,子宫胎盘界面微环境的关键组成部分。