4.5 Article

Pregnancy-associated genes contribute to antiluteolytic mechanisms in ovine corpus luteum

期刊

PHYSIOLOGICAL GENOMICS
卷 45, 期 22, 页码 1095-1108

出版社

AMER PHYSIOLOGICAL SOC
DOI: 10.1152/physiolgenomics.00082.2013

关键词

interferon; corpus luteum; progesterone; luteolysis; pregnancy

资金

  1. Agriculture and Food Research Initiative Competitive Grant [2011-67015-20067]
  2. National Needs Fellowship Grant [2010-38420-20397]
  3. National Center for Research Resources [5P20RR-016469, RR-018788-08]
  4. National Institute for General Medical Science (NIGMS) [8P20GM-103471, GM-103471-09]

向作者/读者索取更多资源

The hypothesis that ovine luteal gene expression differs due to pregnancy status and day of estrous cycle was tested. RNA was isolated from corpora lutea (CL) on days 12 and 14 of the estrous cycle (NP) or pregnancy (P) and analyzed with the Affymetrix bovine microarray. RNA also was isolated from luteal cells on day 10 of estrous cycle that were cultured for 24 h with luteolytic hormones (OXT and PGF) and secretory products of the conceptus (IFNT and PGE2). Differential gene expression (>1.5-fold, P < 0.05) was confirmed using semiquantitative real-time PCR. Serum progesterone concentrations decreased from day 12 to day 15 in NP ewes (P < 0.05) reflecting luteolysis and remained >1.7 ng/ml in P ewes reflecting rescue of the CL. Early luteolysis (days 12-14) was associated with differential expression of 683 genes in the CL, including upregulation of SERPINE1 and THBS1. Pregnancy on day 12 (55 genes) and 14 (734 genes) also was associated with differential expression of genes in the CL, many of which were ISGs (i.e., ISG15, MX1) that were induced when culturing luteal cells with IFNT, but not PGE2. Finally, many genes, such as PTX3, IL6, VEGF, and LHR, were stabilized during pregnancy and downregulated during the estrous cycle and in response to culture of luteal cells with luteolytic hormones. In conclusion, pregnancy circumvents luteolytic pathways and activates or stabilizes genes associated with interferon, chemokine, cell adhesion, cytoskeletal, and angiogenic pathways in the CL.

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