Interleukin (IL)11 mediates protein secretion and modification in human extravillous trophoblasts

被引:29
作者
Sonderegger, Stefan [1 ]
Yap, Joanne [1 ]
Menkhorst, Ellen [1 ]
Weston, Gareth [2 ]
Stanton, Peter G. [1 ]
Dimitriadis, Evdokia [1 ]
机构
[1] Prince Henrys Inst Med Res, Clayton, Vic 3168, Australia
[2] Monash Univ, Monash IVF, Clayton, Vic 3168, Australia
基金
英国医学研究理事会;
关键词
interleukin 11 (IL11); glucose-regulated protein 78 (GRP78); protein disulfide isomerase family A; member 3 (PDIA3); STAT3; proteomic; extravillous trophoblast (EVT); LEUKEMIA INHIBITORY FACTOR; ENDOPLASMIC-RETICULUM; DISULFIDE-ISOMERASE; CELLS; ERP57; PREGNANCY; PHOSPHORYLATION; PLACENTATION; PREECLAMPSIA; IMPLANTATION;
D O I
10.1093/humrep/der259
中图分类号
R71 [妇产科学];
学科分类号
100211 ;
摘要
BACKGROUND: Human trophoblast invasion and differentiation are essential for a successful pregnancy outcome. Dysregulation of these processes can lead to placental pathologies such as pre-eclampsia. The molecular mechanisms; however, are poorly understood. Interleukin (IL)11-a cytokine that regulates endometrial epithelial cell adhesion, trophoblast motility and invasion during implantation-may be involved in some of these processes. METHODS AND RESULTS: The effect of IL11 on protein expression was investigated in trophoblastic HTR8/SVneo cells and primary extravillous trophoblasts (EVTs) purified from first-trimester placentas. Two-dimension (2D)-differential in-gel electrophoresis analyses revealed that 731 spots were significantly differentially regulated by IL11 in HTR8/SVneo cells: seven spots were analyzed by liquid chromatography-tandem mass spectrometry and 14 unique proteins identified. Protein disulfide isomerase family A, member 3 (PDIA3; endoplasmic reticulum p57) and glucose-regulated protein 78 (GRP78) were further validated to be regulated by IL11 in HTR8/SVneo and primary EVT. One dimension western blot analysis confirmed that PDIA3 was down-regulated in EVT. 2D western blot analysis revealed that GRP78 was post-translationally modified following IL11 treatment. Moreover, IL11 stimulated the secretion of GRP78 in EVT. CONCLUSIONS: Data suggest that IL11, possibly via signal transducers and activators of transcription 3 signaling pathway, regulates PDIA3 protein expression and modification/secretion of GRP78. This is the first study to identify PDIA3 and GRP78 as IL11 targets in invasive trophoblasts and identifies a possible mechanism by which IL11 regulates trophoblast function.
引用
收藏
页码:2841 / 2849
页数:9
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