Paria B C, Das N, Das S K, Zhao X, Dileepan K N, Dey S K
Department of Molecular and Integrative Physiology, Ralph L. Smith Research Center, University of Kansas Medical Center, Kansas City 66160-7338, USA.
Endocrinology. 1998 Sep;139(9):3958-66. doi: 10.1210/endo.139.9.6173.
Cell-cell interactions between the blastocyst trophectoderm and uterine luminal epithelium are essential to the process of implantation. The factors that participate in these interactions or their mechanism of actions are poorly understood. Histamine has long been suspected as one of the factors that is involved in implantation. Histamine is formed from L-histidine by histidine decarboxylase (HDC). We examined the expression and regulation of HDC gene in the mouse uterus during early pregnancy and under steroid hormonal stimulation. Northern blot hybridization detected a 2.6-kb transcript of HDC messenger RNA (mRNA) in uterine poly(A)+ RNA samples. Maximum uterine accumulation of HDC mRNA occurred on days 3 and 4 of pregnancy, followed by marked declines on later days (days 5-8). In ovariectomized mice, uterine mRNA levels were up-regulated by an injection of progesterone (P4) by 6 h, and the levels were maintained through 24 h. In contrast, an injection of estradiol-17beta neither stimulated nor antagonized P4-induced HDC mRNA accumulation. P4-induced up-regulation was considerably abrogated by pretreatment with RU-486, a P4 receptor antagonist, suggesting involvement of P4 receptor. In situ hybridization detected HDC mRNA specifically in uterine epithelial cells but not in other cell types. Again, high epithelial accumulation occurred on day 4 of pregnancy. With the progression of implantation (days 5-8), HDC mRNA levels declined in the luminal epithelium surrounding the implanting blastocysts, as compared with that away from the blastocysts. Immunoreactive histamine and HDC were colocalized with HDC mRNA. Western blotting detected a 54-kDa protein in epithelial cell extracts, which also exhibited HDC activity. Expression of HDC in epithelial cells, preceding implantation on day 4, at lower levels after initiation of implantation on day 5, and its regulation by P4 suggest that this gene plays an important role in implantation.
囊胚滋养外胚层与子宫腔上皮之间的细胞间相互作用对于着床过程至关重要。然而,参与这些相互作用的因素及其作用机制仍知之甚少。长期以来,组胺一直被怀疑是参与着床的因素之一。组胺由组氨酸通过组氨酸脱羧酶(HDC)形成。我们研究了妊娠早期和类固醇激素刺激下小鼠子宫中HDC基因的表达和调控。Northern印迹杂交在子宫poly(A)+ RNA样本中检测到一条2.6 kb的HDC信使RNA(mRNA)转录本。HDC mRNA在子宫中的积累在妊娠第3天和第4天达到峰值,随后在后期(第5 - 8天)显著下降。在去卵巢小鼠中,注射孕酮(P4)6小时后子宫mRNA水平上调,并在24小时内保持稳定。相比之下,注射雌二醇-17β既不刺激也不拮抗P4诱导的HDC mRNA积累。P4受体拮抗剂RU - 486预处理可显著消除P4诱导的上调,表明P4受体参与其中。原位杂交检测到HDC mRNA仅在子宫上皮细胞中特异性表达,而在其他细胞类型中未检测到。同样,在妊娠第4天上皮细胞中HDC mRNA积累较高。随着着床的进展(第5 - 8天),与远离囊胚的区域相比,着床囊胚周围的腔上皮中HDC mRNA水平下降。免疫反应性组胺和HDC与HDC mRNA共定位。蛋白质印迹法在上皮细胞提取物中检测到一种54 kDa的蛋白质,其也表现出HDC活性。HDC在第4天着床前的上皮细胞中表达,在第5天着床开始后表达水平降低,且受P4调控,这表明该基因在着床过程中起重要作用。