Czech J. Anim. Sci., 2019, 64(7):317-323 | DOI: 10.17221/21/2019-CJAS

Effect of early pregnancy on the expression of progesterone receptor and progesterone-induced blocking factor 1 in ovine liverOriginal Paper

Leying Zhang, Chen Zhuang, Zimo Zhao, Ning Li, Jiachen Bai, Ling Yang*
Department of Animal Science, College of Life Sciences and Food Engineering, Hebei University of Engineering, Handan, P.R. China

Liver plays important roles in the innate and adaptive immunity, and contributes to the maternal immune adjustments during pregnancy. Progesterone (P4) has key effects on immunomodulation of the maternal uterus during pregnancy. In this study, livers were obtained at day 16 of the estrous cycle and at days 13, 16 and 25 of pregnancy (n = 6 for each group) in ewes. The effects of early pregnancy on the expression of P4 receptor (PGR) and progesterone-induced blocking factor 1 (PIBF1) were analysed through RT-qPCR assay, Western blot and immunohistochemistry analysis. Our results showed that the isoforms of PGR with molecular weights of approximately 60 kDa (PGR60) and 89 kDa (PGR89) were strongly expressed in the livers from pregnant ewes (P < 0.05), but there was no expression of the isoform of PIBF1 with a molecular weight of approximately 55 kDa (PIBF55) on day 13 of pregnancy. The PGR protein was mainly limited to the endothelial cells of the proper hepatic arteries and portal veins, and hepatic cells. In conclusion, the PGR89 and PGR60 were up-regulated, and PIBF55 was down-regulated on day 13 of pregnancy, which may be involved in maternal hepatic immunoregulation during early pregnancy in sheep.

Keywords: ewe; immunoregulation; isoform; progesterone

Published: July 31, 2019  Show citation

ACS AIP APA ASA Harvard Chicago Chicago Notes IEEE ISO690 MLA NLM Turabian Vancouver
Zhang L, Zhuang C, Zhao Z, Li N, Bai J, Yang L. Effect of early pregnancy on the expression of progesterone receptor and progesterone-induced blocking factor 1 in ovine liver. Czech J. Anim. Sci. 2019;64(7):317-323. doi: 10.17221/21/2019-CJAS.
Download citation

References

  1. Bogdan A., Polgar B., Szekeres-Bartho J. (2014): Progesterone induced blocking factor isoforms in normal and failed murine pregnancies. American Journal of Reproductive Immunology, 71, 131-136. Go to original source... Go to PubMed...
  2. Bonney E.A. (2017): Alternative theories: Pregnancy and immune tolerance. Journal of Reproductive Immunology, 123, 65-71. Go to original source... Go to PubMed...
  3. Condon J.C., Hardy D.B., Kovaric K., Mendelson C.R. (2006): Up-regulation of the progesterone receptor (PR)-C isoform in laboring myometrium by activation of nuclear factorkappaB may contribute to the onset of labor through inhibition of PR function. Molecular Endocrinology, 20, 764-775. Go to original source... Go to PubMed...
  4. Doherty D.G. (2016): Immunity, tolerance and autoimmunity in the liver: A comprehensive review. Journal of Autoimmunity, 66, 60-75. Go to original source... Go to PubMed...
  5. Gonzalez-Arenas A., Valadez-Cosmes P., Jimenez-Arellano C., Lopez-Sanchez M., Camacho-Arroyo I. (2014): Progesterone-induced blocking factor is hormonally regulated in human astrocytoma cells, and increases their growth through the IL-4R/JAK1/STAT6 pathway. Journal of Steroid Biochemistry and Molecular Biology, 144, 463-470. Go to original source... Go to PubMed...
  6. Kmiec Z. (2001): Cooperation of liver cells in health and portal veins, and hepatic cells (Figure 3). The staining disease. Advances in Anatomy Embryology and Cell Biolintensity for the PGR was higher in the livers from day 13 of pregnancy than that from day 16 of the estrous cycle, days 16 and 25 of pregnancy (Figure 3). The portal veins and hepatic arteries merge upon ogy, 161, 1-151.
  7. Kowalik M.K., Slonina D., Rekawiecki R., Kotwica J. (2013): Expression of progesterone receptor membrane component (PGRMC) 1 and 2, serpine mRNA binding protein 1 (SERBP1) and nuclear progesterone receptor (PGR) in the bovine endometrium during the estrous cycle and the first trimester of pregnancy. Reproductive Biology, 13, 15-23. Go to original source... Go to PubMed...
  8. Lachmann M., Gelbmann D., Kalman E., Polgar B., Buschle M., Von Gabain A., Szekeres-Bartho J., Nagy E. (2004): PIBF (progesterone induced blocking factor) is overexpressed in highly proliferating cells and associated with the centrosome. International Journal of Cancer, 112, 51-60. Go to original source... Go to PubMed...
  9. Livak K.J., Schmittgen T.D. (2001): Analysis of relative gene expression data using real-time quantitative PCR and the 2-ΔΔCt method. Methods, 25, 402-408. Go to original source... Go to PubMed...
  10. Lonard D.M., O'Malley B.W. (2012): Nuclear receptor coregulators: Modulators of pathology and therapeutic targets. Nature Reviews Endocrinology, 8, 598-604. Go to original source... Go to PubMed...
  11. Mi Y., Lin A., Fiete D., Steirer L., Baenziger J.U. (2014): Modulation of mannose and asialoglycoprotein receptor expression determines glycoprotein hormone half-life at during early pregnancy in ruminants. Journal of Dairy Science, 99, 5941-5950.
  12. Szekeres-Bartho J., Falkay G., Torok A., Pacsa A.S. (1985a): The mechanism of the inhibitory effect of progesterone on lymphocyte cytotoxicity: II. Relationship between cytotoxicity and the cyclooxygenase pathway of arachidonic acid metabolism. American Journal of Reproductive Immunology and Microbiology, 9, 19-22. Go to original source... Go to PubMed...
  13. Szekeres-Bartho J., Kilar F., Falkay G., Csernus V., Torok A., Pacsa A.S. (1985b): The mechanism of the inhibitory effect of progesterone on lymphocyte cytotoxicity: I. Progesterone-treated lymphocytes release a substance inhibiting cytotoxicity and prostaglandin synthesis. American Journal of Reproductive Immunology and Microbiology, 9, 15-18. Go to original source... Go to PubMed...
  14. Szekeres-Bartho J., Wegmann T.G. (1996): A progesteronecritical points in the reproductive cycle. Journal of Biologi- dependent immunomodulatory protein alters the Th1/Th2 cal Chemistry, 289, 12157-12167. Go to original source... Go to PubMed...
  15. Micks E., Raglan G.B., Schulkin J. (2015): Bridging progestogens in pregnancy and pregnancy prevention. Endocrine Connections, 4, R81-R92. Go to original source... Go to PubMed...
  16. Parker G.A., Picut C.A. (2012): Immune functioning in non lymphoid organs: The liver. Toxicologic Pathology, 40, 237-247. Go to original source... Go to PubMed...
  17. Polgar B., Kispal G., Lachmann M., Paar C., Nagy E., Csere P., Miko E., Szereday L., Varga P., Szekeres-Bartho J. (2003): Molecular cloning and immunologic characterization of a novel cDNA coding for progesterone-induced blocking factor. Journal of Immunology, 171, 5956-5963. Go to original source... Go to PubMed...
  18. Raghupathy R., Al-Mutawa E., Al-Azemi M., Makhseed M., Azizieh F., Szekeres-Bartho J. (2009): Progesterone-induced blocking factor (PIBF) modulates cytokine production by lymphocytes from women with recurrent miscarriage or preterm delivery. Journal of Reproductive Immunology, 80, 91-99. Go to original source... Go to PubMed...
  19. Simmen R.C., Simmen F.A. (2002): Progesterone receptors and Sp/Krüppel-like family members in the uterine endometrium. Frontiers in Bioscience, 7, d1556-d1565. Go to original source... Go to PubMed...
  20. Slonina D., Kowalik M.K., Kotwica J. (2012): Expression of progesterone receptor membrane component 1, serpine mRNA binding protein 1 and nuclear progesterone receptor isoforms A and B in the bovine myometrium during the estrous cycle and early pregnancy. Journal of Reproduction and Development, 58, 288-294. Go to original source... Go to PubMed...
  21. Spencer T.E., Bazer F.W. (1995): Temporal and spatial alterations in uterine estrogen receptor and progesterone receptor gene expression during the estrous cycle and early pregnancy in the ewe. Biology of Reproduction, 53, 1527-1543. Go to original source... Go to PubMed...
  22. Spencer T.E., Forde N., Lonergan P. (2016): The role of progesterone and conceptus-derived factors in uterine biology balance. Journal of Reproductive Immunology, 31, 81-95.
  23. Topletz A.R., Le H.N., Lee N., Chapman J.D., Kelly E.J., Wang J., Isoherranen N. (2013): Hepatic Cyp2d and Cyp26a1 mRNAs and activities are increased during mouse pregnancy. Drug Metabolism and Disposition, 41, 312-319. Go to original source... Go to PubMed...
  24. Yang L., Zhang L.Y., Qiao H.Y., Liu N., Wang Y.X., Li S.J. (2014): Maternal immune regulation by conceptus during early pregnancy in the bovine. Asian Journal of Animal and Veterinary Advances, 9, 610-620. Go to original source...
  25. Yang L., Zang S., Bai Y., Yao X., Zhang L. (2017): Effect of early pregnancy on the expression of progesterone receptor and progesterone-induced blocking factor in ovine lymph node. Theriogenology, 93, 78-83. Go to original source... Go to PubMed...
  26. Yang L., Guo R., Yao X., Yan J., Bai Y., Zhang L. (2018): Expression of progesterone receptor and progesterone-induced blocking factor in the spleen during early pregnancy in ewes. Livestock Science, 209, 14-19. Go to original source...
  27. Zakar T., Mesiano S. (2011): How does progesterone relax the uterus in pregnancy? New England Journal of Medicine, 364, 972-973. Go to original source... Go to PubMed...
  28. Zhang L., Mi H., Yan J., Yan X., Yang L. (2017): Pregnancyassociated changes in expression of progesterone receptor and progesterone-induced blocking factor genes in bone marrow of ewes. Animal Reproduction Science, 186, 77-84. Go to original source... Go to PubMed...
  29. Zhang L., Xue J., Wang Q., Lv W., Mi H., Liu Y., Yang L. (2018): Changes in expression of ISG15, progesterone receptor and progesterone-induced blocking factor in ovine thymus during early pregnancy. Theriogenology, 121, 153-159. Go to original source... Go to PubMed...
  30. Zou Y., Hu M., Bao Q., Chan J.Y., Dai G. (2013): Nrf2 participates in regulating maternal hepatic adaptations to pregnancy. Journal of Cell Science, 126, 1618-1625. Go to original source... Go to PubMed...

This is an open access article distributed under the terms of the Creative Commons Attribution-NonCommercial 4.0 International (CC BY NC 4.0), which permits non-comercial use, distribution, and reproduction in any medium, provided the original publication is properly cited. No use, distribution or reproduction is permitted which does not comply with these terms.