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S100A8, S100A9, and S100A12: Expression and Regulation During the Estrous Cycle in Pigs

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한국동물생명공학회(구 한국수정란이식학회) (Journal of Animal Reproduction & Biotechnology)
초록

S100As are calcium-binding proteins with two EF-hand calcium-binding motifs. In several studies, S100A proteins are described to play important roles in pro-inflammatory responses including damage-associated molecular pattern (DAMP) signaling and in the establishment of pregnancy. However, the role of S100As have not been determined in the uterine endometrium during the estrous cycle in pigs. Thus, this study was performed to investigate expression and regulation of S100A8, S100A9, and S100A12 in the uterine endometrial tissues during the estrous cycle in pigs. Real-time RT-PCR analysis showed that S100A8, S100A9, and S100A12 mRNAs were expressed in the uterine endometrium during the estrous cycle with higher levels on days 15 and 18 of the estrous cycle than other days of cycle. To investigate the effects of steroid hormones, estradiol (E2) and progesterone (P4), on expression of S100A8, S100A9, and S100A12 mRNAs, endometrial tissue explants from immature pigs were treated with steroid hormones. Levels of S100A8, S100A9, and S100A12 were increased by the treatment of P4, and the increased levels of S100A8, S100A9, and S100A12 by P4 were not inhibited by the treatment of progesterone receptor antagonist, RU486. However, levels of S100A8, S100A9, and S100A12 were decreased by treatment of MEK inhibitor, U0126. These results exhibited that S100As were expressed in the uterine endometrium during the estrous cycle in a cyclic stage-specific manner, and their expression was affected by P4. These suggest that S100As may play an important role in endometrial function during the proestrous period of the estrous cycle in pigs. [Supported by the Next Generation Biogreen 21 program (#PJ01119103), Rural Development Administration, and by Korea Research Foundation (#2015R1D1A1A01058356)]

저자
  • Hwanhee Jang(Division of Biological Science and Technology, Yonsei University, Wonju, 26493 Republic of Korea)
  • Inkyu Yu(Division of Biological Science and Technology, Yonsei University, Wonju, 26493 Republic of Korea)
  • Jisoo Han(Division of Biological Science and Technology, Yonsei University, Wonju, 26493 Republic of Korea)
  • Minjeong Kim(Division of Biological Science and Technology, Yonsei University, Wonju, 26493 Republic of Korea)
  • Soogil Chae(Division of Biological Science and Technology, Yonsei University, Wonju, 26493 Republic of Korea)
  • Suhyung Lee(Division of Biological Science and Technology, Yonsei University, Wonju, 26493 Republic of Korea)
  • Hakhyun Ka(Division of Biological Science and Technology, Yonsei University, Wonju, 26493 Republic of Korea)