Paria B C, Das S K, Huet-Hudson Y M, Dey S K
Department of Obstetrics-Gynecology, Ralph L. Smith Research Center, University of Kansas Medical Center, Kansas City 66160-7338.
Biol Reprod. 1994 Mar;50(3):481-91. doi: 10.1095/biolreprod50.3.481.
Temporal and cell-type specific distribution of transforming growth factor alpha (TGF alpha) precursor (proTGF alpha) was examined in the mouse uterus during the periimplantation period, and after steroid hormone treatments of ovariectomized adult mice by immunohistochemistry using antibodies that recognize the precursor forms of the growth factor. These studies were complemented by immunoblot analysis of proTGF alpha in separated uterine cell-type preparations. The specificity of the antibodies used in these studies was confirmed by use of pancreas or lactating mammary glands from transgenic mice in which mutated proTGF alpha, lacking recognition sites for proteolytic cleavages, was targeted for expression under a tissue-specific enhancer/promoter. Analysis of histochemical studies revealed accumulation of immunoreactive proTGF alpha primarily in luminal and glandular epithelial cells on Day 1 of pregnancy or pseudopregnancy followed by little or no accumulation on Days 2 and 3. However, immunoreactive proTGF alpha started to reappear in the luminal epithelium on the morning of Day 4 and became more prominent in the afternoon. In pregnant mice, immunostaining persisted in these cells at the implantation sites during the time of attachment reaction (2130 h on Day 4), but disappeared by morning of Day 5. Immunostaining appeared to be situated at the apical border of the luminal epithelium. No positive immunostaining could be detected in the nonreceptive uterus on Day 5 or 6 of pseudopregnancy. Consistent with the immunohistochemistry results, Western blot analysis detected two species of precursor proteins (14.5 and 17 kDa) in isolated luminal epithelial cell-enriched preparations on Day 4, but not on Day 5, of pseudopregnancy. The results suggest that proTGF alpha accumulates in the luminal epithelium of the receptive uterus prior to implantation. The effects of ovarian steroids on uterine accumulation of proTGF alpha were examined in ovariectomized adult mice by immunohistochemistry and immunoblotting. Whereas an injection of estradiol-17 beta (E2) or progesterone (P4) had little or a modest effect on epithelial accumulation of proTGF alpha, P4 priming for several days resulted in distinct accumulation of proTGF alpha in epithelial cells. The superimposition of an E2 treatment on P4 priming showed a biphasic response, with an initial gradual loss of immunostaining through 12 h followed by a return by 24 h of E2 treatment. The combined hormone treatment schedule employed here is similar to the situation of inducing implantation with E2 in P4-primed delayed implanting mice. The results suggest a paracrine/"juxtacrine" role for this growth factor in implantation.
在围植入期的小鼠子宫中,以及在对成年去卵巢小鼠进行类固醇激素处理后,使用识别生长因子前体形式的抗体,通过免疫组织化学检测转化生长因子α(TGFα)前体(proTGFα)的时间和细胞类型特异性分布。这些研究通过对分离的子宫细胞类型制剂中的proTGFα进行免疫印迹分析得到补充。在这些研究中使用的抗体的特异性通过使用来自转基因小鼠的胰腺或泌乳乳腺得到证实,在转基因小鼠中,缺乏蛋白水解切割识别位点的突变proTGFα在组织特异性增强子/启动子的控制下表达。组织化学研究分析显示,在妊娠或假妊娠第1天,免疫反应性proTGFα主要在腔上皮和腺上皮细胞中积累,而在第2天和第3天积累很少或没有积累。然而,免疫反应性proTGFα在第4天上午开始重新出现在腔上皮中,并在下午变得更加明显。在妊娠小鼠中,在附着反应时(第4天21:30),植入部位的这些细胞中免疫染色持续存在,但在第5天上午消失。免疫染色似乎位于腔上皮的顶端边界。在假妊娠第5天或第6天的未接受子宫中未检测到阳性免疫染色。与免疫组织化学结果一致,免疫印迹分析在假妊娠第4天的分离的富含腔上皮细胞的制剂中检测到两种前体蛋白(14.5和17 kDa),但在第5天未检测到。结果表明,proTGFα在植入前在接受子宫的腔上皮中积累。通过免疫组织化学和免疫印迹分析研究了卵巢类固醇对子宫proTGFα积累的影响。注射雌二醇-17β(E2)或孕酮(P4)对proTGFα的上皮积累影响很小或有适度影响,而P4预处理几天导致proTGFα在上皮细胞中明显积累。在P4预处理基础上叠加E2处理显示出双相反应,最初在12小时内免疫染色逐渐消失,随后在E2处理24小时后恢复。这里采用的联合激素处理方案类似于在P4预处理的延迟植入小鼠中用E2诱导植入的情况。结果表明这种生长因子在植入中具有旁分泌/“邻分泌”作用。