...
首页> 外文期刊>AJRI: American Journal of Reproductive Immunology >Decidual NK Cell-Derived Conditioned Medium (dNK-CM) Mediates VEGF-C Secretion in Extravillous Cytotrophoblasts
【24h】

Decidual NK Cell-Derived Conditioned Medium (dNK-CM) Mediates VEGF-C Secretion in Extravillous Cytotrophoblasts

机译:蜕膜NK细胞衍生条件培养基(dNK-CM)介导绒毛滋养细胞中VEGF-C的分泌。

获取原文
获取原文并翻译 | 示例
           

摘要

The regulatory mechanisms involved in VEGF-C secretion by trophoblasts during placentation are poorly understood. We investigated whether or not decidual natural killer cell conditioned medium (dNK-CM) stimulated VEGF-C secretion in the extravillous cytotrophoblast (EVT) cell line HTR8/SVneo. Method of Study The effects of dNK-CM and recombinant IFN-γ on VEGF-C induction by HTR8/SVneo were studied in the absence or presence of IFN-γ or its receptor blocking antibodies, p38 inhibitor (SB202190), JAK inhibitor (JAK inhibitor-1, JI-1), and on STAT1 knockdown HTR8/SVneo. VEGF-C was quantified by ELISA. FACS was used to investigate the phosphorylations of Tyr701 or Ser727 of STAT1 on stimulated HTR8/SVneo. Results dNK-CM facilitated VEGF-C secretion by HTR8/SVneo. IFN-γ and IFN-γR1 or IFN-γR2 blocking antibodies reduced both dNK-CM- and IFN-γ-induced VEGF-C secretion. Phosphorylations on Tyr701 or Ser727 of STAT1 were elevated upon stimulation. Secretion of VEGF-C was reduced by treatment with SB202190, JI-1, or STAT1 knockdown by siRNA. Conclusion VEGF-C production by trophoblasts is regulated by soluble factors secreted by dNK through p38 and JAK-STAT1 pathways.
机译:人们对胎盘滋养细胞中滋养细胞分泌VEGF-C的调控机制了解甚少。我们调查了蜕膜性自然杀伤细胞条件培养基(dNK-CM)是否刺激了绒毛滋养层细胞(EVT)细胞HTR8 / SVneo中的VEGF-C分泌。研究方法在不存在或存在IFN-γ或其受体阻断抗体,p38抑制剂(SB202190),JAK抑制剂(JAK)的情况下,研究了dNK-CM和重组IFN-γ对HTR8 / SVneo诱导VEGF-C诱导的影响。抑制剂1(JI-1)和STAT1敲低的HTR8 / SVneo。通过ELISA定量VEGF-C。 FACS用于研究刺激的HTR8 / SVneo上STAT1的Tyr701或Ser727的磷酸化。结果dNK-CM促进HTR8 / SVneo分泌VEGF-C。 IFN-γ和IFN-γR1或IFN-γR2阻断抗体减少了dNK-CM-和IFN-γ诱导的VEGF-C分泌。刺激后STAT1的Tyr701或Ser727上的磷酸化升高。通过用siRNA进行SB202190,JI-1或STAT1敲低处理,可减少VEGF-C的分泌。结论滋养细胞产生的VEGF-C受dNK通过p38和JAK-STAT1途径分泌的可溶性因子的调控。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号