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Published in: Reproductive Biology and Endocrinology 1/2015

Open Access 01-12-2015 | Research

In vitro decidualisation of canine uterine stromal cells

Authors: Ewa Kautz, Paula de Carvalho Papa, Iris M. Reichler, Aykut Gram, Alois Boos, Mariusz P. Kowalewski

Published in: Reproductive Biology and Endocrinology | Issue 1/2015

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Abstract

Background

The uterine response to the presence of embryos is poorly understood in the domestic dog (Canis familiaris). The intimate embryo-maternal cross-talk, which begins following the hatching of blastocysts and embryo attachment leads to strong structural and functional remodelling of the uterus. A part of this process is decidualisation, comprising morphological and biochemical changes that result in formation of maternal stroma-derived decidual cells. These are an integral part of the canine placenta materna, which together with the maternal vascular endothelium are the only cells of the canine endotheliochorial placenta able to resist trophoblast invasion. These cells are also the only ones within the canine placenta expressing the progesterone receptor (PGR). Understanding the decidualisation process thus appears essential for understanding canine reproductive physiology.

Methods

Here, we investigated the capability of canine uterine stromal cells to decidualise in vitro, thereby serving as a canine model of decidualisation. A dbcAMP-mediated approach was chosen during a time course of 24 - 72 h. Tissue material from six (n = 6) healthy, dioestric bitches was used (approximately 2 weeks after ovulation). Cells were characterized by differential staining, nearly 100 % of which were vimentin-positive. Scanning and transmission electron microscope analyses were applied, and morphological changes were recorded with a live cell imaging microscope. Expression of several decidualisation markers was investigated.

Results

The in vitro cultured stromal cells acquired characteristics of decidual cells when incubated with 0.5 mM dbcAMP for 72 h. Their shape changed from elongated to rounded, while ultrastructural analysis revealed higher numbers of mitochondria and secretory follicles, and an increased proliferation rate. Elevated expression levels of IGF1, IGF2, PRLR and ERα were observed in decidualised cells; PRL and ERβ remained mostly below the detection limit, while PGR remained unaffected. The expression of smooth muscle α actin (αSMA), another decidualisation marker, was strongly induced. Among prostaglandin system members, levels of COX2 (PTGS2) and of PGE2-synthase (PTGES) were upregulated. Expression of the PGE2 receptors, PTGER2 and PTGER4, was clearly detectable.

Conclusion

An in vitro decidualisation model with canine uterine stromal cells was successfully established, allowing future, more detailed studies to be undertaken on the underlying molecular and endocrine mechanisms of canine decidualisation.
Appendix
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Literature
1.
go back to reference Gellersen B, Brosens IA, Brosens JJ. Decidualization of the human endometrium: mechanisms, functions, and clinical perspectives. Semin Reprod Med. 2007;25(6):445–53.PubMedCrossRef Gellersen B, Brosens IA, Brosens JJ. Decidualization of the human endometrium: mechanisms, functions, and clinical perspectives. Semin Reprod Med. 2007;25(6):445–53.PubMedCrossRef
2.
4.
go back to reference Frolova A, Flessner L, Chi M, Kim ST, Foyouzi-Yousefi N, Moley KH. Facilitative glucose transporter type 1 is differentially regulated by progesterone and estrogen in murine and human endometrial stromal cells. Endocrinology. 2009;150(3):1512–20.PubMedCentralPubMedCrossRef Frolova A, Flessner L, Chi M, Kim ST, Foyouzi-Yousefi N, Moley KH. Facilitative glucose transporter type 1 is differentially regulated by progesterone and estrogen in murine and human endometrial stromal cells. Endocrinology. 2009;150(3):1512–20.PubMedCentralPubMedCrossRef
5.
go back to reference Sharkey AM, Smith SK. The endometrium as a cause of implantation failure. Best Pract Res Clin Obstet Gynaecol. 2003;17(2):289–307.PubMedCrossRef Sharkey AM, Smith SK. The endometrium as a cause of implantation failure. Best Pract Res Clin Obstet Gynaecol. 2003;17(2):289–307.PubMedCrossRef
6.
go back to reference Jauniaux E, Jurkovic D. Placenta accreta: pathogenesis of a 20th century iatrogenic uterine disease. Placenta. 2012;33(4):244–51.PubMedCrossRef Jauniaux E, Jurkovic D. Placenta accreta: pathogenesis of a 20th century iatrogenic uterine disease. Placenta. 2012;33(4):244–51.PubMedCrossRef
7.
go back to reference Al-Bassam MA, Thomson RG, O’Donnell L. Involution abnormalities in the postpartum uterus of the bitch. Veter pathol. 1981;18(2):208–18. Al-Bassam MA, Thomson RG, O’Donnell L. Involution abnormalities in the postpartum uterus of the bitch. Veter pathol. 1981;18(2):208–18.
8.
go back to reference Nishiyama T, Tsumagari S, Ito M, Kimura J, Watanabe G, Taya K, et al. Immunohistochemical study of steroidogenic enzymes in the ovary and placenta during pregnancy in the dog. Anat Histol Embryol. 1999;28(2):125–9.PubMedCrossRef Nishiyama T, Tsumagari S, Ito M, Kimura J, Watanabe G, Taya K, et al. Immunohistochemical study of steroidogenic enzymes in the ovary and placenta during pregnancy in the dog. Anat Histol Embryol. 1999;28(2):125–9.PubMedCrossRef
9.
go back to reference Hoffmann B, Hoveler R, Nohr B, Hasan SH. Investigations on hormonal changes around parturition in the dog and the occurrence of pregnancy-specific non conjugated oestrogens. Exp Clin Endocrinol. 1994;102(3):185–9.PubMedCrossRef Hoffmann B, Hoveler R, Nohr B, Hasan SH. Investigations on hormonal changes around parturition in the dog and the occurrence of pregnancy-specific non conjugated oestrogens. Exp Clin Endocrinol. 1994;102(3):185–9.PubMedCrossRef
10.
go back to reference Concannon PW, McCann JP, Temple M. Biology and endocrinology of ovulation, pregnancy and parturition in the dog. J Reprod Fertil Suppl. 1989;39:3–25.PubMed Concannon PW, McCann JP, Temple M. Biology and endocrinology of ovulation, pregnancy and parturition in the dog. J Reprod Fertil Suppl. 1989;39:3–25.PubMed
11.
go back to reference Hoffmann B, Hoveler R, Hasan SH, Failing K. Ovarian and pituitary function in dogs after hysterectomy. J Reprod Fertil. 1992;96(2):837–45.PubMedCrossRef Hoffmann B, Hoveler R, Hasan SH, Failing K. Ovarian and pituitary function in dogs after hysterectomy. J Reprod Fertil. 1992;96(2):837–45.PubMedCrossRef
12.
go back to reference Thatcher WW, Bartol FF, Knickerbocker JJ, Curl JS, Wolfenson D, Bazer FW, et al. Maternal recognition of pregnancy in cattle. J Dairy Sci. 1984;67(11):2797–811.PubMedCrossRef Thatcher WW, Bartol FF, Knickerbocker JJ, Curl JS, Wolfenson D, Bazer FW, et al. Maternal recognition of pregnancy in cattle. J Dairy Sci. 1984;67(11):2797–811.PubMedCrossRef
13.
go back to reference Bazer FW, Thatcher WW, Hansen PJ, Mirando MA, Ott TL, Plante C. Physiological mechanisms of pregnancy recognition in ruminants. J Reprod Fertil Suppl. 1991;43:39–47.PubMed Bazer FW, Thatcher WW, Hansen PJ, Mirando MA, Ott TL, Plante C. Physiological mechanisms of pregnancy recognition in ruminants. J Reprod Fertil Suppl. 1991;43:39–47.PubMed
14.
go back to reference Perry JS, Heap RB, Amoroso EC. Steroid hormone production by pig blastocysts. Nature. 1973;245(54):45–7.PubMedCrossRef Perry JS, Heap RB, Amoroso EC. Steroid hormone production by pig blastocysts. Nature. 1973;245(54):45–7.PubMedCrossRef
15.
go back to reference Kautz E, Gram A, Aslan S, Ay SS, Selcuk M, Kanca H, et al. Expression of genes involved in the embryo-maternal interaction in the early-pregnant canine uterus. Reproduction. 2014;147(5):703–17.PubMedCrossRef Kautz E, Gram A, Aslan S, Ay SS, Selcuk M, Kanca H, et al. Expression of genes involved in the embryo-maternal interaction in the early-pregnant canine uterus. Reproduction. 2014;147(5):703–17.PubMedCrossRef
16.
go back to reference Frasor J, Gaspar CA, Donnelly KM, Gibori G, Fazleabas AT. Expression of prolactin and its receptor in the baboon uterus during the menstrual cycle and pregnancy. J Clin Endocrinol Metab. 1999;84(9):3344–50.PubMed Frasor J, Gaspar CA, Donnelly KM, Gibori G, Fazleabas AT. Expression of prolactin and its receptor in the baboon uterus during the menstrual cycle and pregnancy. J Clin Endocrinol Metab. 1999;84(9):3344–50.PubMed
17.
go back to reference Goffin V, Binart N, Touraine P, Kelly PA. Prolactin: the new biology of an old hormone. Annu Rev Physiol. 2002;64:47–67.PubMedCrossRef Goffin V, Binart N, Touraine P, Kelly PA. Prolactin: the new biology of an old hormone. Annu Rev Physiol. 2002;64:47–67.PubMedCrossRef
18.
go back to reference Amoroso EC. Placentation. In: Parkers AS, editor. Marshall’s physiology of reproduction. London: Longmans Green; 1952. p. 127–316. Amoroso EC. Placentation. In: Parkers AS, editor. Marshall’s physiology of reproduction. London: Longmans Green; 1952. p. 127–316.
19.
go back to reference Kehrer A. Chorionic development and structure of the placenta zonaria in the cat, dog and fox (author’s transl). Z Anat Entwicklungsgesch. 1973;143:25–42.PubMedCrossRef Kehrer A. Chorionic development and structure of the placenta zonaria in the cat, dog and fox (author’s transl). Z Anat Entwicklungsgesch. 1973;143:25–42.PubMedCrossRef
20.
go back to reference Kowalewski MP, Beceriklisoy HB, Pfarrer C, Aslan S, Kindahl H, Kucukaslan I, et al. Canine placenta: a source of prepartal prostaglandins during normal and antiprogestin-induced parturition. Reproduction. 2010;139(3):655–64.PubMedCrossRef Kowalewski MP, Beceriklisoy HB, Pfarrer C, Aslan S, Kindahl H, Kucukaslan I, et al. Canine placenta: a source of prepartal prostaglandins during normal and antiprogestin-induced parturition. Reproduction. 2010;139(3):655–64.PubMedCrossRef
21.
go back to reference Vermeirsch H, Simoens P, Lauwers H. Immunohistochemical detection of the estrogen receptor-alpha and progesterone receptor in the canine pregnant uterus and placental labyrinth. Anat Rec. 2000;260(1):42–50.PubMedCrossRef Vermeirsch H, Simoens P, Lauwers H. Immunohistochemical detection of the estrogen receptor-alpha and progesterone receptor in the canine pregnant uterus and placental labyrinth. Anat Rec. 2000;260(1):42–50.PubMedCrossRef
22.
go back to reference Gram A, Boos A, Kowalewski MP. Uterine and placental expression of canine oxytocin receptor during pregnancy and normal and induced parturition. Reprod Domest Anim. 2014;49(Suppl (2), 2):41–9.PubMedCrossRef Gram A, Boos A, Kowalewski MP. Uterine and placental expression of canine oxytocin receptor during pregnancy and normal and induced parturition. Reprod Domest Anim. 2014;49(Suppl (2), 2):41–9.PubMedCrossRef
23.
go back to reference Brar AK, Frank GR, Kessler CA, Cedars MI, Handwerger S. Progesterone-dependent decidualization of the human endometrium is mediated by cAMP. Endocrine. 1997;6(3):301–7.PubMedCrossRef Brar AK, Frank GR, Kessler CA, Cedars MI, Handwerger S. Progesterone-dependent decidualization of the human endometrium is mediated by cAMP. Endocrine. 1997;6(3):301–7.PubMedCrossRef
24.
go back to reference Gellersen B, Brosens J. Cyclic AMP and progesterone receptor cross-talk in human endometrium: a decidualizing affair. J Endocrinol. 2003;178(3):357–72.PubMedCrossRef Gellersen B, Brosens J. Cyclic AMP and progesterone receptor cross-talk in human endometrium: a decidualizing affair. J Endocrinol. 2003;178(3):357–72.PubMedCrossRef
25.
go back to reference Kim JJ, Fazleabas AT. Uterine receptivity and implantation: the regulation and action of insulin-like growth factor binding protein-1 (IGFBP-1), HOXA10 and forkhead transcription factor-1 (FOXO-1) in the baboon endometrium. Reprod Biol Endocrin. 2004;2:34.CrossRef Kim JJ, Fazleabas AT. Uterine receptivity and implantation: the regulation and action of insulin-like growth factor binding protein-1 (IGFBP-1), HOXA10 and forkhead transcription factor-1 (FOXO-1) in the baboon endometrium. Reprod Biol Endocrin. 2004;2:34.CrossRef
26.
go back to reference Tamura I, Asada H, Maekawa R, Tanabe M, Lee L, Taketani T, et al. Induction of IGFBP-1 expression by cAMP is associated with histone acetylation status of the promoter region in human endometrial stromal cells. Endocrinology. 2012;153(11):5612–21.PubMedCrossRef Tamura I, Asada H, Maekawa R, Tanabe M, Lee L, Taketani T, et al. Induction of IGFBP-1 expression by cAMP is associated with histone acetylation status of the promoter region in human endometrial stromal cells. Endocrinology. 2012;153(11):5612–21.PubMedCrossRef
27.
go back to reference Kowalewski MP, Fox B, Gram A, Boos A, Reichler I. Prostaglandin E2 functions as a luteotrophic factor in the dog. Reproduction. 2013;145(3):213–26.PubMedCrossRef Kowalewski MP, Fox B, Gram A, Boos A, Reichler I. Prostaglandin E2 functions as a luteotrophic factor in the dog. Reproduction. 2013;145(3):213–26.PubMedCrossRef
28.
go back to reference Kowalewski MP, Schuler G, Taubert A, Engel E, Hoffmann B. Expression of cyclooxygenase 1 and 2 in the canine corpus luteum during diestrus. Theriogenology. 2006;66(6–7):1423–30.PubMedCrossRef Kowalewski MP, Schuler G, Taubert A, Engel E, Hoffmann B. Expression of cyclooxygenase 1 and 2 in the canine corpus luteum during diestrus. Theriogenology. 2006;66(6–7):1423–30.PubMedCrossRef
29.
go back to reference Kowalewski MP, Mason JI, Howie AF, Morley SD, Schuler G, Hoffmann B. Characterization of the canine 3beta-hydroxysteroid dehydrogenase and its expression in the corpus luteum during diestrus. J Steroid Biochem Mol Biol. 2006;101(4–5):254–62.PubMedCrossRef Kowalewski MP, Mason JI, Howie AF, Morley SD, Schuler G, Hoffmann B. Characterization of the canine 3beta-hydroxysteroid dehydrogenase and its expression in the corpus luteum during diestrus. J Steroid Biochem Mol Biol. 2006;101(4–5):254–62.PubMedCrossRef
30.
go back to reference Wild P. Electron microscopy of viruses and virus-cell interactions. Method Cell Biol. 2008;88:497–524.CrossRef Wild P. Electron microscopy of viruses and virus-cell interactions. Method Cell Biol. 2008;88:497–524.CrossRef
31.
go back to reference Kowalewski MP, Michel E, Gram A, Boos A, Guscetti F, Hoffmann B, et al. Luteal and placental function in the bitch: spatio-temporal changes in prolactin receptor (PRLr) expression at dioestrus, pregnancy and normal and induced parturition. Reprod Biol Endocrin. 2011;9:109.CrossRef Kowalewski MP, Michel E, Gram A, Boos A, Guscetti F, Hoffmann B, et al. Luteal and placental function in the bitch: spatio-temporal changes in prolactin receptor (PRLr) expression at dioestrus, pregnancy and normal and induced parturition. Reprod Biol Endocrin. 2011;9:109.CrossRef
32.
go back to reference Kowalewski MP, Meyer A, Hoffmann B, Aslan S, Boos A. Expression and functional implications of peroxisome proliferator-activated receptor gamma (PPARgamma) in canine reproductive tissues during normal pregnancy and parturition and at antiprogestin induced abortion. Theriogenology. 2011;75(5):877–86.PubMedCrossRef Kowalewski MP, Meyer A, Hoffmann B, Aslan S, Boos A. Expression and functional implications of peroxisome proliferator-activated receptor gamma (PPARgamma) in canine reproductive tissues during normal pregnancy and parturition and at antiprogestin induced abortion. Theriogenology. 2011;75(5):877–86.PubMedCrossRef
33.
go back to reference Gram A, Buechler U, Boos A, Hoffmann B, Kowalewski MP. Biosynthesis and degradation of canine placental prostaglandins: prepartum changes in expression and function of prostaglandin F2alpha-synthase (PGFS, AKR1C3) and 15-hydroxyprostaglandin dehydrogenase (HPGD). Biol Reprod. 2013;89(1):2.PubMedCrossRef Gram A, Buechler U, Boos A, Hoffmann B, Kowalewski MP. Biosynthesis and degradation of canine placental prostaglandins: prepartum changes in expression and function of prostaglandin F2alpha-synthase (PGFS, AKR1C3) and 15-hydroxyprostaglandin dehydrogenase (HPGD). Biol Reprod. 2013;89(1):2.PubMedCrossRef
34.
go back to reference Gram A, Fox B, Buchler U, Boos A, Hoffmann B, Kowalewski MP. Canine placental prostaglandin E2 synthase: expression, localization, and biological functions in providing substrates for prepartum PGF2alpha synthesis. Biol Reprod. 2014;91(6):154.PubMedCrossRef Gram A, Fox B, Buchler U, Boos A, Hoffmann B, Kowalewski MP. Canine placental prostaglandin E2 synthase: expression, localization, and biological functions in providing substrates for prepartum PGF2alpha synthesis. Biol Reprod. 2014;91(6):154.PubMedCrossRef
35.
go back to reference Alam SM, Konno T, Dai G, Lu L, Wang D, Dunmore JH, et al. A uterine decidual cell cytokine ensures pregnancy-dependent adaptations to a physiological stressor. Development. 2007;134(2):407–15.PubMedCrossRef Alam SM, Konno T, Dai G, Lu L, Wang D, Dunmore JH, et al. A uterine decidual cell cytokine ensures pregnancy-dependent adaptations to a physiological stressor. Development. 2007;134(2):407–15.PubMedCrossRef
36.
go back to reference Dudley DJ, Trautman MS, Araneo BA, Edwin SS, Mitchell MD. Decidual cell biosynthesis of interleukin-6: regulation by inflammatory cytokines. J Clin Endocrinol Metab. 1992;74(4):884–9.PubMedCrossRef Dudley DJ, Trautman MS, Araneo BA, Edwin SS, Mitchell MD. Decidual cell biosynthesis of interleukin-6: regulation by inflammatory cytokines. J Clin Endocrinol Metab. 1992;74(4):884–9.PubMedCrossRef
37.
go back to reference Golander A, Hurley T, Barrett J, Hizi A, Handwerger S. Prolactin synthesis by human chorion-decidual tissue: a possible source of prolactin in the amniotic fluid. Science. 1978;202(4365):311–3.PubMedCrossRef Golander A, Hurley T, Barrett J, Hizi A, Handwerger S. Prolactin synthesis by human chorion-decidual tissue: a possible source of prolactin in the amniotic fluid. Science. 1978;202(4365):311–3.PubMedCrossRef
38.
go back to reference Ganeff C, Chatel G, Munaut C, Frankenne F, Foidart JM, Winkler R. The IGF system in in-vitro human decidualization. Mol Hum Reprod. 2009;15(1):27–38.PubMedCrossRef Ganeff C, Chatel G, Munaut C, Frankenne F, Foidart JM, Winkler R. The IGF system in in-vitro human decidualization. Mol Hum Reprod. 2009;15(1):27–38.PubMedCrossRef
39.
go back to reference Lane B, Oxberry W, Mazella J, Tseng L. Decidualization of human endometrial stromal cells in vitro: effects of progestin and relaxin on the ultrastructure and production of decidual secretory proteins. Hum Reprod. 1994;9(2):259–66.PubMed Lane B, Oxberry W, Mazella J, Tseng L. Decidualization of human endometrial stromal cells in vitro: effects of progestin and relaxin on the ultrastructure and production of decidual secretory proteins. Hum Reprod. 1994;9(2):259–66.PubMed
40.
go back to reference Tang B, Gurpide E. Direct effect of gonadotropins on decidualization of human endometrial stroma cells. J Steroid Biochem Mol Biol. 1993;47(1–6):115–21.PubMedCrossRef Tang B, Gurpide E. Direct effect of gonadotropins on decidualization of human endometrial stroma cells. J Steroid Biochem Mol Biol. 1993;47(1–6):115–21.PubMedCrossRef
41.
go back to reference Anaf V, Simon P, Fayt I, Noel J. Smooth muscles are frequent components of endometriotic lesions. Hum Reprod. 2000;15(4):767–71.PubMedCrossRef Anaf V, Simon P, Fayt I, Noel J. Smooth muscles are frequent components of endometriotic lesions. Hum Reprod. 2000;15(4):767–71.PubMedCrossRef
42.
go back to reference Wang HS, Chard T. IGFs and IGF-binding proteins in the regulation of human ovarian and endometrial function. J Endocrinol. 1999;161(1):1–13.PubMedCrossRef Wang HS, Chard T. IGFs and IGF-binding proteins in the regulation of human ovarian and endometrial function. J Endocrinol. 1999;161(1):1–13.PubMedCrossRef
43.
go back to reference Yu J, Wu J, Bagchi IC, Bagchi MK, Sidell N, Taylor RN. Disruption of gap junctions reduces biomarkers of decidualization and angiogenesis and increases inflammatory mediators in human endometrial stromal cell cultures. Mol Cell Endocrinol. 2011;344(1–2):25–34.PubMedCentralPubMedCrossRef Yu J, Wu J, Bagchi IC, Bagchi MK, Sidell N, Taylor RN. Disruption of gap junctions reduces biomarkers of decidualization and angiogenesis and increases inflammatory mediators in human endometrial stromal cell cultures. Mol Cell Endocrinol. 2011;344(1–2):25–34.PubMedCentralPubMedCrossRef
44.
go back to reference Wathes DC, Reynolds TS, Robinson RS, Stevenson KR. Role of the insulin-like growth factor system in uterine function and placental development in ruminants. J Dairy Sci. 1998;81(6):1778–89.PubMedCrossRef Wathes DC, Reynolds TS, Robinson RS, Stevenson KR. Role of the insulin-like growth factor system in uterine function and placental development in ruminants. J Dairy Sci. 1998;81(6):1778–89.PubMedCrossRef
45.
go back to reference Tseng L, Mazella J. Prolactin and its receptor in human endometrium. Semin Reprod Med. 1999;17(1):23–7.CrossRef Tseng L, Mazella J. Prolactin and its receptor in human endometrium. Semin Reprod Med. 1999;17(1):23–7.CrossRef
46.
go back to reference Prigent-Tessier A, Tessier C, Hirosawa-Takamori M, Boyer C, Ferguson-Gottschall S, Gibori G. Rat decidual prolactin. Identification, molecular cloning, and characterization. J Biol Chem. 1999;274(53):37982–9.PubMedCrossRef Prigent-Tessier A, Tessier C, Hirosawa-Takamori M, Boyer C, Ferguson-Gottschall S, Gibori G. Rat decidual prolactin. Identification, molecular cloning, and characterization. J Biol Chem. 1999;274(53):37982–9.PubMedCrossRef
47.
go back to reference Jabbour HN, Critchley HO, Boddy SC. Expression of functional prolactin receptors in nonpregnant human endometrium: janus kinase-2, signal transducer and activator of transcription-1 (STAT1), and STAT5 proteins are phosphorylated after stimulation with prolactin. J Clin Endocrinol Meta. 1998;83(7):2545–53.CrossRef Jabbour HN, Critchley HO, Boddy SC. Expression of functional prolactin receptors in nonpregnant human endometrium: janus kinase-2, signal transducer and activator of transcription-1 (STAT1), and STAT5 proteins are phosphorylated after stimulation with prolactin. J Clin Endocrinol Meta. 1998;83(7):2545–53.CrossRef
48.
go back to reference Concannon P, Tsutsui T, Shille V. Embryo development, hormonal requirements and maternal responses during canine pregnancy. J Repdo Fertil Suppl. 2001;57:169–79. Concannon P, Tsutsui T, Shille V. Embryo development, hormonal requirements and maternal responses during canine pregnancy. J Repdo Fertil Suppl. 2001;57:169–79.
49.
go back to reference Concannon PW. Endocrinologic control of normal canine ovarian function. Reprod Domest Anim. 2009;44 Suppl 2:3–15.PubMedCrossRef Concannon PW. Endocrinologic control of normal canine ovarian function. Reprod Domest Anim. 2009;44 Suppl 2:3–15.PubMedCrossRef
50.
go back to reference Handwerger S, Markoff E, Richards R. Regulation of the synthesis and release of decidual prolactin by placental and autocrine/paracrine factors. Placenta. 1991;12(2):121–30.PubMedCrossRef Handwerger S, Markoff E, Richards R. Regulation of the synthesis and release of decidual prolactin by placental and autocrine/paracrine factors. Placenta. 1991;12(2):121–30.PubMedCrossRef
51.
go back to reference Parhar RS, Yagel S, Lala PK. PGE2-mediated immunosuppression by first trimester human decidual cells blocks activation of maternal leukocytes in the decidua with potential anti-trophoblast activity. Cell Immunol. 1989;120(1):61–74.PubMedCrossRef Parhar RS, Yagel S, Lala PK. PGE2-mediated immunosuppression by first trimester human decidual cells blocks activation of maternal leukocytes in the decidua with potential anti-trophoblast activity. Cell Immunol. 1989;120(1):61–74.PubMedCrossRef
52.
go back to reference Ziecik AJ, Waclawik A, Kaczmarek MM, Blitek A, Jalali BM, Andronowska A. Mechanisms for the establishment of pregnancy in the pig. Reprod Domest Anim. 2011;46 Suppl 3:31–41.PubMed Ziecik AJ, Waclawik A, Kaczmarek MM, Blitek A, Jalali BM, Andronowska A. Mechanisms for the establishment of pregnancy in the pig. Reprod Domest Anim. 2011;46 Suppl 3:31–41.PubMed
53.
go back to reference Kowalewski MP, Mutembei HM, Hoffmann B. Canine prostaglandin E2 synthase (PGES) and its receptors (EP2 and EP4): expression in the corpus luteum during dioestrus. Anim Reprod Sci. 2008;109(1–4):319–29.PubMedCrossRef Kowalewski MP, Mutembei HM, Hoffmann B. Canine prostaglandin E2 synthase (PGES) and its receptors (EP2 and EP4): expression in the corpus luteum during dioestrus. Anim Reprod Sci. 2008;109(1–4):319–29.PubMedCrossRef
54.
go back to reference Kowalewski MP, Beceriklisoy HB, Aslan S, Agaoglu AR, Hoffmann B. Time related changes in luteal prostaglandin synthesis and steroidogenic capacity during pregnancy, normal and antiprogestin induced luteolysis in the bitch. Anim Reprod Sci. 2009;116(1–2):129–38.PubMedCrossRef Kowalewski MP, Beceriklisoy HB, Aslan S, Agaoglu AR, Hoffmann B. Time related changes in luteal prostaglandin synthesis and steroidogenic capacity during pregnancy, normal and antiprogestin induced luteolysis in the bitch. Anim Reprod Sci. 2009;116(1–2):129–38.PubMedCrossRef
55.
go back to reference Kowalewski MP, Ihle S, Siemieniuch MJ, Gram A, Boos A, Zdunczyk S, et al. Formation of the early canine CL and the role of prostaglandin E2 (PGE2) in regulation of its function: An in vivo approach. Theriogenology. 2015;83(6):1038–47.PubMedCrossRef Kowalewski MP, Ihle S, Siemieniuch MJ, Gram A, Boos A, Zdunczyk S, et al. Formation of the early canine CL and the role of prostaglandin E2 (PGE2) in regulation of its function: An in vivo approach. Theriogenology. 2015;83(6):1038–47.PubMedCrossRef
Metadata
Title
In vitro decidualisation of canine uterine stromal cells
Authors
Ewa Kautz
Paula de Carvalho Papa
Iris M. Reichler
Aykut Gram
Alois Boos
Mariusz P. Kowalewski
Publication date
01-12-2015
Publisher
BioMed Central
Published in
Reproductive Biology and Endocrinology / Issue 1/2015
Electronic ISSN: 1477-7827
DOI
https://doi.org/10.1186/s12958-015-0066-4

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