Dunlap Kathrin A, Erikson David W, Burghardt Robert C, White Frank J, Reed Kristey M, Farmer Jennifer L, Spencer Thomas E, Magness Ronald R, Bazer Fuller W, Bayless Kayla J, Johnson Greg A
Department of Veterinary Integrative Biosciences, College of Veterinary Medicine and Biomedical Sciences, Texas A&M University, College Station, Texas 77843, USA.
Biol Reprod. 2008 Nov;79(5):983-90. doi: 10.1095/biolreprod.108.071068. Epub 2008 Jul 30.
Secreted phosphoprotein one (SPP1, osteopontin) may regulate conceptus implantation and placentation. We investigated effects of progesterone (P(4)) and the conceptus on expression and localization of SPP1 in the ovine uterus. Steady-state levels of SPP1 mRNA in the endometrium of unilaterally pregnant ewes did not differ significantly between nongravid and gravid horns within their respective days of pregnancy; however, levels did increase as pregnancy progressed. SPP1 mRNA was detectable in the glandular epithelium (GE) of both nongravid and gravid horns via in situ hybridization. SPP1 protein was localized to the apical surface of the luminal epithelium of both nongravid and gravid uterine horns. Gravid horns exhibited extensive stromal SPP1 on Days 40 through 120, whereas SPP1 was markedly lower in the stroma of nongravid uterine horns through Day 80 of pregnancy. By Day 120, stromal expression of SPP1 between nongravid and gravid horns was similar. Long-term P(4) treatment of ovariectomized ewes induced SPP1 in the uterine stroma and GE. A bioactive 45-kDa SPP1 fragment was purified from uterine secretions and promoted ovine trophectoderm cell attachment in vitro. Interestingly, increased stromal cell expression of SPP1 was positively associated with vascularization as assessed by von Willebrand factor staining. Finally, ovine uterine artery endothelial cells produced SPP1 during outgrowth into three-dimensional collagen matrices in an in vitro model system that recapitulates angiogenesis. Collectively, P(4) induces and the conceptus further stimulates SPP1 in uterine GE and stroma, where SPP1 likely influences histotrophic and hematotrophic support of conceptus development.
分泌磷蛋白1(SPP1,骨桥蛋白)可能调节孕体着床和胎盘形成。我们研究了孕酮(P4)和孕体对绵羊子宫中SPP1表达和定位的影响。单侧妊娠母羊子宫内膜中SPP1 mRNA的稳态水平在妊娠相应天数的非妊娠角和妊娠角之间无显著差异;然而,随着妊娠进展,其水平确实升高。通过原位杂交在非妊娠角和妊娠角的腺上皮(GE)中均可检测到SPP1 mRNA。SPP1蛋白定位于非妊娠和妊娠子宫角腔上皮的顶端表面。在妊娠第40天至120天,妊娠角的基质中SPP1广泛表达,而在妊娠第80天之前,非妊娠子宫角基质中的SPP1明显较低。到妊娠第120天,非妊娠角和妊娠角之间基质中SPP1的表达相似。对去卵巢母羊进行长期P4处理可诱导子宫基质和GE中SPP1的表达。从子宫分泌物中纯化出一种具有生物活性的45 kDa SPP1片段,其在体外可促进绵羊滋养外胚层细胞附着。有趣的是,通过血管性血友病因子染色评估,基质细胞中SPP1表达的增加与血管生成呈正相关。最后,在一个模拟血管生成的体外模型系统中,绵羊子宫动脉内皮细胞在生长到三维胶原基质的过程中产生SPP1。总之,P4诱导并由孕体进一步刺激子宫GE和基质中的SPP1,其中SPP1可能影响孕体发育的组织营养和血液营养支持。