Halling A
Department of Anatomy, University of Lund, Sweden.
J Steroid Biochem Mol Biol. 1993 Mar;44(3):227-37. doi: 10.1016/0960-0760(93)90083-9.
Proteins released during incubation in vitro of oviductal and uterine tissues from 8-week-old female NMRI mice treated neonatally with diethylstilbestrol (DES) or vehicle were studied. The objective was to study if neonatal DES treatment altered the patterns of proteins released from the oviduct and uterus, as earlier studies had shown a detrimental effect of the oviductal environment in DES exposed females on early embryo development. In separate experiments nonlabeled and 35S-labeled proteins released from oviductal/uterine tissues during organ incubations were characterized with 1 and 2D gel electrophoresis. The incubation media of both oviducts and uteri from DES females had increased levels of a serum derived nonlabeled protein, identified as apolipoprotein A1. The amount of this protein in the incubation medium was not influenced by previous ovariectomy but increased by in vivo treatment with estradiol, in both ovariectomized controls and DES treated females. Three other unlabeled proteins were consistently found in higher amounts in the incubation media from DES exposed oviduct/uterine tissue, than in incubates of control tissue. In tissue incubates of oviducts from DES females, three synthesized proteins (35 kDa-pl 6.2, 112 and 143 kDa) were released in lower amounts and two in higher amounts (53 kDa-pl 6.6 and 53 kDa-pl 6.8) than in controls. In uterus from DES treated females one labeled protein was released in increased amounts (80 kDa-pl 6.7) and one in decreased amounts (43 kDa-pl 6.6), when compared with controls. In estrogen induced uterine luminal fluid from 8-week-old DES treated females the levels of four proteins (26, 42, 53 and 97 kDa) were increased and two (24 and 32 kDa) were decreased. These results show permanent alterations in levels of secreted proteins in both the oviduct and uterus of adult but neonatally DES treated females, which could be of importance for their poor reproductive performance.
研究了新生期用己烯雌酚(DES)或赋形剂处理的8周龄雌性NMRI小鼠输卵管和子宫组织在体外孵育期间释放的蛋白质。目的是研究新生期DES处理是否改变了输卵管和子宫释放蛋白质的模式,因为早期研究表明,DES暴露雌性的输卵管环境对早期胚胎发育有不利影响。在单独的实验中,用一维和二维凝胶电泳对器官孵育期间从输卵管/子宫组织释放的未标记和35S标记蛋白质进行了表征。DES雌性小鼠输卵管和子宫的孵育培养基中,一种血清来源的未标记蛋白质(鉴定为载脂蛋白A1)水平升高。该蛋白质在孵育培养基中的含量不受先前卵巢切除术的影响,但在去卵巢对照组和DES处理的雌性小鼠中,通过体内雌二醇处理会增加。在DES暴露的输卵管/子宫组织的孵育培养基中,始终发现另外三种未标记蛋白质的含量高于对照组织的孵育物。在DES雌性小鼠的输卵管组织孵育物中,与对照相比,三种合成蛋白质(35 kDa-pI 6.2、112和143 kDa)释放量较低,两种释放量较高(53 kDa-pI 6.6和53 kDa-pI 6.8)。与对照相比,DES处理的雌性小鼠子宫中一种标记蛋白质的释放量增加(80 kDa-pI 6.7),一种减少(43 kDa-pI 6.6)。在8周龄DES处理的雌性小鼠雌激素诱导的子宫腔液中,四种蛋白质(26、42、53和97 kDa)的水平升高,两种(24和32 kDa)降低。这些结果表明,成年但新生期接受DES处理的雌性小鼠的输卵管和子宫中分泌蛋白质水平发生了永久性改变,这可能对它们较差的生殖性能具有重要意义。