期刊文献+

CD74及MIF表达对子痫前期巨噬细胞-胎盘滋养层相互作用的影响 被引量:1

Effect of CD74 expression on macrophage-placental trophoblast interaction in preeclampsia
原文传递
导出
摘要 子痫前期是一种较为严重的妊娠期并发症,临床上一般以血压升高为主要表现,伴随蛋白尿等症状,严重者可以危及母婴生命。近年来研究表明该病是由许多因素引起,但是确切病因并未十分明确。巨噬细胞-胎盘滋养层之间相互作用的平衡对于正常妊娠的发生有着重要影响,其中CD74及巨噬细胞迁移抑制因子(MIF)的正常表达对于巨噬细胞-滋养细胞之间的相互作用有着重要的意义,也是目前研究重点之一,本文将对CD74及MIF对子痫前期胎盘巨噬细胞-滋养层之间相互作用的影响进行综述,以期进一步探索该病的发病机制。 Preeclampsia is a serious complication of pregnancy, mainly characterized by hypertension and proteinuria and other clinical manifestations. Severe cases can endanger the lives of mothers and infants. In recent years, studies have shown that preeclampsia is caused by a variety of factors, although the specific cause is not very clear. The balance of placental macrophage-trophoblast interactions plays an important role in the development of normal pregnancy. Normal expression of cluster of differentiation 74(CD74) and MIF plays an important role in the interaction between placental macrophages and trophoblast cells, which is one of the focuses of current research. Here we will review the role of CD74 and MIF in placental macrophage-trophoblast interaction in preeclampsia in order to further explore the pathogenesis of this disease.
作者 王亭婷 严瑾 郑英 孔祥 Wang Tingting;Yan Jin;Zheng Ying;Kong Xiang(Department of Obstetrics and Gynecology,Clinical Medical College of Yangzhou University,Yangzhou 225001,China)
出处 《中华临床医师杂志(电子版)》 CAS 2017年第19期2289-2292,共4页 Chinese Journal of Clinicians(Electronic Edition)
关键词 巨噬细胞-滋养层细胞相互作用 CD74 巨噬细胞迁移抑制因子 胎盘形成 子痫前期 Macrophage-trophoblast cell interactions CD74 MIF Placenta formation Preeclampsia
  • 相关文献

参考文献6

二级参考文献94

  • 1Simons D, Grieb G, Hristov M, et al. Hypoxia - induced endothelial secretion of maerophage migration inhibitory fac- tor and role in endothelial progenitor cell recruitment. J Cell Mol Med,2011,15 : 668 - 678.
  • 2Rosado Jde D, Rodriguez-Sosa M. Macrophage migration In- hibitory factor (MIF) : a key player in protozoan infections. Int J Biol Sci,2011,7 : 1239 - 1258.
  • 3Grieb G, Merk M, Bemhagen J, et al. Macrophage migra- tion inhibitory factor (MIF) : a promising biomarker. Drug News Perspeet,2010,23 : 257 - 264.
  • 4Lue H, Thiele M, Franz J, et al. Maerophage migration in- hibitory factor (MIF) promotes cell survival by activation of the Akt pathway and role for CSN5/JAB1 in the control of autocrine MIF activity. Oncogene ,2007,26 : 5046 - 5059.
  • 5Bemhagen J, Krohn R, Lue H, et al. MIF is a noneognate ligand of CXC ehemokine receptors in inflammatory and atherogenic cell recruitment. Nat Med, 2007, 13 : 587 596.
  • 6Schwartz V, Krtittgen A, Weis J, et al. Role for CD74 and CXCR4 in clathrin-dependent endocytosis of the cytokine MIF. Eur J Cell Biol,2012,91 : 435 -449.
  • 7Lue H, Dewor M, Leng L, et al. Activation of the JNK sig- nalling pathway by macrophage migration inhibitory factor (MIF) and dependence on CXCR4 and CD74. Cell Signal, 2011,23 : 135-144.
  • 8Gesser B, Rasmussen M, Raaby L, et al. Dimethylfumarate inhibits MIF-induced proliferation of keratinocytes by inhibi- ting MSK1 and RSK1 activation and by inducing nuclear pc-Jun ( S63 ) and p-p53 ( S15 ) expression. Inflamm Res, 2011,60 : 643 -653.
  • 9Sivaram G, Tiwari SK, Bardia A, et al. Maerophage migra- tion inhibitory factor, Toll-like receptor 4, and CD14 poly- morphisms with altered expression levels in patients with ul- cerative colitis. Hum Immunol,2012,73 : 201 - 205.
  • 10Salminen A, Kaarniranta K. Control of p53 and NF-KB sig- naling by WIP1 and MIF: role in cellular senescence and organismal aging. Cell Signal ,2011,23: 747 - 752.

共引文献201

同被引文献7

引证文献1

二级引证文献12

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部