A genomic and proteomic investigation of the impact of preimplantation factor on human decidual cells

被引:65
作者
Paidas, Michael J. [1 ]
Krikun, Graciela [2 ]
Huang, S. Joseph [2 ]
Jones, Richard [3 ]
Romano, Michael [1 ]
Annunziato, Jack [1 ]
Barnea, Eytan R. [4 ,5 ]
机构
[1] Yale Univ, Sch Med, Dept Obstet Gynecol & Reprod Sci, Yale Women & Childrens Ctr Blood Disorders, New Haven, CT 06520 USA
[2] Yale Univ, Sch Med, Dept Obstet Gynecol & Reprod Sci, Reprod Biol Unit, New Haven, CT 06520 USA
[3] NextGen Sci Inc, Ann Arbor, MI USA
[4] Soc Invest Early Pregnancy, Cherry Hill, NJ USA
[5] Univ Med & Dent New Jersey, Robert Wood Johnson Med Sch, Dept Obstet Gynecol & Reprod, Camden, NJ 08103 USA
关键词
decidual cells; genomics; implantation; preimplantation factor; proteomics; FACTOR PIF; INFLAMMATORY CYTOKINES; HUMAN-PREGNANCY; EXPRESSION; EMBRYO; TOLERANCE; IMMUNOSUPPRESSION; MENSTRUATION; LYMPHOCYTES; HEMOSTASIS;
D O I
10.1016/j.ajog.2010.03.024
中图分类号
R71 [妇产科学];
学科分类号
100211 ;
摘要
OBJECTIVE: Preimplantation factor (PIF) is a novel, 15 amino acid peptide, secreted by viable embryos. This study aims to elucidate PIF's effects in human endometrial stromal cells (HESC) decidualized by estrogen and progestin, which mimics the preimplantation milieu, and in first-trimester decidua cultures (FTDC). STUDY DESIGN: HESC or FTDC were incubated with 100 nmol/L synthetic PIF or vehicle control. Global gene expression was analyzed using microarray and pathway analysis. Proteins were analyzed using quantitative mass spectrometry, and PIF binding by protein array. RESULTS: Gene and proteomic analysis demonstrate that PIF affects immune, adhesion, and apoptotic pathways. Significant up-regulation in HESC (fold change) include: nuclear factor-k-beta activation via interleukin-1 receptor-associated kinase binding protein 1 (53); Toll-like receptor 5 (9); FK506 binding protein 15, 133kDa protein (2.3); and Down syndrome cell adhesion molecule like 1 (16). B-cell lymphoma protein 2 was down-regulated in HESC(21.1) and FTDC(27.1). Protein array demonstrates PIF interaction with intracellular targets insulin-degrading enzyme and beta-K+ channels. CONCLUSION: PIF displays essential multitargeted effects, of regulating immunity, promoting embryo-decidual adhesion, and regulating adaptive apoptotic processes.
引用
收藏
页码:459.e1 / 459.e8
页数:8
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