RSS-Feed abonnieren
DOI: 10.1055/s-2008-1042408
© J. A. Barth Verlag in Georg Thieme Verlag KG Stuttgart · New York
Placental Steroids in Cattle: Hormones, Placental Growth Factors or By-products of Trophoblast Giant Cell Differentiation?
Publikationsverlauf
received 05.12.2007
first decision 20.12.2007
accepted 15.01.2008
Publikationsdatum:
25. März 2008 (online)
Abstract
The bovine placenta produces large amounts of steroids, mainly estrone (E1) and progesterone (P4). Specific features of bovine placental steroidogenesis are 1) the expression of all enzymes needed for the production of estrogens from cholesterol in the trophoblast 2) an only marginal and temporal contribution to peripheral maternal P4 levels restricted to a period between approx. days 150–240 of gestation 3) the predominance of sulfoconjugated over free E1 and 4) a complementary setting of steroidogenic enzymes in the two morphologically discriminable trophoblast cell types, the uninucleated trophoblast cells (UTC) and the trophoblast giant cells (TGC). In cattle so far no definite information is available on the specific biological roles of placental estrogens and P4. However, the detection of estrogen receptors and progesterone receptors in the placentomes suggests a role primarily as local regulators of caruncular growth, differentiation and functions. Inconsistent with a function as a caruncular growth factor is the strong evidence that in cattle placental estrogens enter the maternal compartment almost completely as estrone sulfate (E1S), which is not active at classical nuclear receptors. On the other hand, E1S may be converted locally to free active estrogens via the action of steroid sulfatase (StS), which has been detected in specific parts of the bovine caruncular epithelium. Alternatively or in addition, StS expression in the caruncular epithelium may serve the utilization of sulfated neutral steroid precursors (e.g. pregnenolone sulfate or cholesterol sulfate) supplied with maternal blood, thus providing free substrates for further metabolization in the adjacent trophoblast. The down-regulation of P450scc and P450c17 and the up-regulation of 3ß-HSD and aromatase during the differentiation of TGC from UTC in parallel with the up-regulation of ERß and estrogen sulfotransferase in maturing TGC suggests a function of placental estrogens primarily as auto- or intracrine regulators during this process and assigns to conjugated placental estrogens a role as inactivated by-products of TGC differentiation intended for excretion. Collectively, despite some evidence from recent studies for putative roles of placental steroids in cattle their exact functions in the bovine species remain still undefined.
Key words
cattle - placenta - steroidogenic enzymes - steroid receptors
References
- 1 Arai KY, Tanaka Y, Taniyama H, Tsunoda N, Nambo Y, Nagamine N, Watanabe G, Taya K. Expression of inhibins, activins, insulin-like growth factor-I and steroidogenic enzymes in the equine placenta. Domest Anim Endocrinol. 2006; 31 19-34
- 2 Ben-David E, Shemesh M. Ultrastructural localization of cytochrome P-450scc in the bovine placentome using protein A-gold technique. Biol Reprod. 1990; 42 131-138
- 3 Ben-Zimra M, Koler M, Melamed-Book N, Arensburg J, Payne AH, Orly J. Uterine and placental expression of steroidogenic genes during rodent pregnancy. Mol Cell Endocrinol. 2002; 187 223-231
- 4 Brown JM, Adams JB, Beattie CW. Production and characterization of a monoclonal antibody to bovine estrogen sulfotransferase. Hybridoma. 1987; 6 413-422
- 5 Bukovsky A, Caudle MR, Cekanova M, Fernando RI, Wimalasena J, Foster JS, Henley DC, Elder RF. Placental expression of estrogen receptor beta and its hormone binding variant -comparison with estrogen receptor alpha and a role for estrogen receptors in asymmetric division and differentiation of estrogen-dependent cells. Reprod Biol Endocrinol. 2003; 15 1:36
- 6 Chapman E, Best MD, Hanson SR, Wong CH. Sulfotransferases: structure, mechanism, biological activity, inhibition, and synthetic utility. Angew Chem Int Ed Engl. 2004; 43 3526-3548
- 7 Conley AJ, Bird IM. The role of cytochrome P450 17alpha-hydroxylase and 3beta-hydroxysteroid dehydrogenase in the integration of gonadal and adrenal steroidogenesis via the delta5 and delta4 pathways of steroidogenesis in mammals. Biol Reprod. 1997; 56 789-799
- 8 Conley AJ, Ford SP. Effect of prostaglandin F2 alpha-induced luteolysis on in vivo and in vitro progesterone production by individual placentomes of cows. J Anim Sci. 1987; 65 500-507
-
9 Conley AJ, Mason JI. Endocrine function of the placenta. In: Thorburn GD, Harding R (eds).
Textbook of Fetal Physiology . Oxford: Oxford University Press 1994: 16-29 - 10 Cronier L, Guibourdenche J, Niger C, Malassine A. Oestradiol stimulates morphological and functional differentiation of human villous cytotrophoblast. Placenta. 1999; 20 669-676
- 11 Day AM. Cloprostenol for termination of pregnancy in cattle. B) The induction of abortion. N Z Vet J. 1977; 25 139-144
- 12 Diczfalusy E. Endocrine functions of the human fetoplacental unit. Federation Proceedings. 1964; 23 791-798
- 13 Eley RM, Thatcher WW, Bazer FW. Hormonal and physical changes associated with bovine conceptus development. J Reprod Fertil. 1979; 55 181-190
- 14 Elias PM, Williams ML, Maloney ME, Bonifas JA, Brown BE, Grayson S, Epstein Jr EH. Stratum corneum lipids in disorders of cornification. Steroid sulfatase and cholesterol sulfate in normal desquamation and the pathogenesis of recessive X-linked ichthyosis. J Clin Invest. 1984; 74 1414-1421
- 15 Elias PM, Crumrine D, Rassner U, Hachem JP, Menon GK, Man W, Choy MH, Leypoldt L, Feingold KR, Williams ML. Basis for abnormal desquamation and permeability barrier dysfunction in RXLI. J Invest Dermatol. 2004; 122 314-319
- 16 Estergreen VL, Frost OL, Gomes WR, Erb RE, Bullard JF. Effect of ovariectomy on pregnancy maintenance and parturition in dairy cows. J Dairy Sci. 1967; 50 1293-1295
- 17 Evans G, Wagner WC. In vitro oestrogen synthesis by bovine placenta during pregnancy and induced parturition. Acta Endocrinol (Copenh). 1981; 98 119-125
- 18 Greven H, Kowalewski MP, Hoffmann B, Geyer J, Rex-Haffner M, Ugele B, Schuler G. Bovine placental steroid sulphatase: Molecular cloning and expression pattern in placentomes during gestation and at parturition. Placenta. 2007; 28 889-897
- 19 Hall JM, MacDonnell DP. Coregulators in nuclear estrogen receptor action: from concept to therapeutic targeting. Mol Interv. 2005; 5 343-357
- 20 Hähnel R, Twaddle E, Ratajczak T. The specificity of the estrogen receptor of human uterus. J Steroid Biochem. 1973; 4 21-31
- 21 Hansen PJ. Regulation of uterine immune function by progesterone – lessons from the sheep. J Reprod Immunol. 1998; 40 63-79
- 22 Hoedemaker M, Weston PG, Wagner WC. Influence of cortisol and different steroidogenic pathways on estrogen synthesis by the bovine placenta. Am J Vet Res. 1990; 51 1012-1015
-
23 Hoffmann B.
Bestimmung von Steroidhormonen beim weiblichen Rind; Entwicklung von Messverfahren und physiologische Daten . Habilitationsschrift TU München-Weihenstephan 1972 - 24 Hoffmann B. Untersuchungen zur Steroidhormonsynthese in der Plazenta des Rindes. Wien tierärztl Mschr. 1983; 70 224-228
- 25 Hoffmann B, Wagner WC, Gimenez T. Free and conjugated steroids in maternal and fetal plasma in the cow near term. Biol Reprod. 1976; 15 126-133
- 26 Hoffmann B, Wagner WC, Hixon JE, Bahr J. Observations concerning the functional status of the corpus luteum and the placenta around parturition in the cow. Anim Reprod Sci. 1979; 2 253-266
- 27 Hoffmann B, Höveler 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; 102 185-189
- 28 Hoffmann B, Goes de Pinho T, Schuler G. Determination of free and conjugated oestrogens in peripheral blood plasma, feces and urine of cattle throughout pregnancy. Exp Clin Endocrinol Diabetes. 1997; 105 296-303
- 29 Hoffmann B, Falter K, Vielemeier A, Failing K, Schuler G. Investigations on the activity of bovine placental oestrogen sulfotransferase and –sulfatase from midgestation to parturition. Exp Clin Endocrinol Diabetes. 2001; 109 294-301
- 30 Hoffmann B, Schuler G. The bovine placenta; a source and target of steroid hormones: observations during the second half of gestation. Domest Anim Endocrinol. 2002; 23 309-320
- 31 Janowski T, Zdunczyk S, Podhalicz-Dziegielewska M, Rasz A, Chmielewski A. Effect of oestrogen antagonist (tamoxifen) on steroid hormone levels, maturation process of placentomes and course of late pregnancy in cows. Reprod Domest Anim. 1996; 31 379-384
- 32 Janowski T, Zdunczyk S, Malecki-Tepicht J, Baranski W, Ras A. Mammary secretion of oestrogens in the cow. Domest Anim Endocrinol. 2002; 23 125-137
- 33 Janszen BPM, Bevers MM, Tol HTM Van, Dieleman SJ, Weijden GC van der, Taverne MAM. Oestrogen sulphatase activity in endometrium and foetal membranes of late gestational and parturient cows. Anim Reprod Sci. 1995; 37 251-256
- 34 Johnson WH, Manns JG, Adams WM, Mapletoft RJ. Termination of pregnancy with cloprostenol and dexamethasone in intact or ovariectomized cows. Can Vet J. 1981; 22 288-290
- 35 Klisch K, Hecht W, Pfarrer C, Schuler G, Hoffmann B, Leiser R. DNA content and ploidy level of bovine placentomal trophoblast giant cells. Placenta. 1999a; 20 451-458
- 36 Klisch K, Pfarrer C, Schuler G, Hoffmann B, Leiser R. Tripolar acytokinetic mitosis and formation of feto-maternal syncytia in the bovine placentome: different modes of the generation of multinuclear cells. Anat Embryol (Berl). 1999b; 200 229-237
- 37 Kuiper GG, Carlsson B, Grandien K, Enmark E, Haggblad J, Nilsson S, Gustafsson JA. Comparison of the ligand binding specificity and transcript tissue distribution of estrogen receptors alpha and beta. Endocrinology. 1997; 138 863-870
- 38 Kuss E. The fetoplacental unit of primates. Exp Clin Endocrinol. 1994; 102 135-165
- 39 Leiser R, Kaufmann P. Placental structure, in a comparative aspect. Exp Clin Endocrinol. 1994; 102 122-134
- 40 Mattioli M, Gaiani R, Bono G, Chiesa F. Estrone to estrone sulfate conversion and viceversa in bovine placentome. Arch Vet Ital. 1984; 35 22-26
- 41 Meyer HHD. Luteal versus placental progesterone: the situation in the cow, pig and bitch. Exp Clin Endocrinol. 1994; 102 190-192
- 42 Nash AR, Glenn WK, Moore SS, Kerr J, Thompson AR, Thompson EO. Oestrogen sulfotransferase: molecular cloning and sequencing of cDNA for the bovine placental enzyme. Aust J Biol Sci. 1988; 41 507-516
- 43 Nishiyama T, Tsumagari S, Ito M, Kimura J, Watanabe G, Taya K, Takeishi M. Immunohistochemical study of steroidogenic enzymes in the ovary and placenta during pregnancy in the dog. Anat Histol Embryol. 1999; 28 125-129
- 44 Özalp GR. Lokalisation der 17α-Hydroxylase-C17,20-Lyase (P450c17), 3β-Hydroxysteroiddehydrogenase-Δ4/5 Isomerase (3β-HSD) und Aromatase (P450arom) in der Plazenta beim Rind im Verlauf der Gravidität. , Diss vet med, Giessen, 2005; http://geb.uni-giessen.de/geb/volltexte/2005/2005/
- 45 Pashen RL, Allen WR. The role of the fetal gonads and placenta in steroid production, maintenance of pregnancy and parturition in the mare. J Reprod Fertil. 1979; 27 ((Suppl)) 499-509
- 46 Pepe GJ, Albrecht ED. Regulation of functional differentiation of the placental villous syncytiotrophoblast by estrogen during primate pregnancy. Steroids. 1999; 64 624-627
- 47 Rama S, Petrusz P, Rao AJ. Hormonal regulation of human trophoblast differentiation: a possible role for 17beta-estradiol and GnRH. Mol Cell Endocrinol. 2004; 218 79-94
- 48 Reed MJ, Purohit A, Woo LW, Newman SP, Potter BV. Steroid sulfatase: molecular biology, regulation, and inhibition. Endocr Rev. 2005; 26 171-202
- 49 Reimers TJ, Ullmann MB, Hansel W. Progesterone and prostanoid production by bovine binucleate trophoblastic cells. Biol Reprod. 1985; 33 1227-1236
- 50 Rhee HS, Oh SH, Ko BJ, Han DM, Jeon BH, Park H, Moon HB, Kim WS. Expression of 3beta-hydroxysteroid dehydrogenase and P450 side chain cleavage enzyme in the human uterine endometrium. Exp Mol Med. 2003; 35 160-166
- 51 Salido EC, Yen PH, Barajas L, Shapiro LJ. Steroid sulfatase expression in human placenta: immunocytochemistry and in situ hybridization study. J Clin Endocrinol Metab. 1990; 70 1564-1567
- 52 Santner SJ, Feil PD, Santen RJ. In situ estrogen production via the estrone sulfatase pathway in breast tumors: relative importance versus the aromatase pathway. J Clin Endocrinol Metab. 1984; 59 29-33
- 53 Schlafer DH, Fisher PJ, Davies CJ. The bovine placenta before and after birth: placental development and function in health and disease. Anim Reprod Sci. 2000; 60–61 145-160
- 54 Schuler G, Hartung F, Hoffmann B. Investigations on the use of C-21-steroids as precursors for placental oestrogen synthesis in the cow. Exp Clin Endocrinol. 1994; 102 169-174
- 55 Schuler G, Wirth C, Klisch K, Pfarrer C, Leiser R, Hoffmann B. Immunolocalization of progesterone receptors in bovine placentomes throughout mid and late gestation and at parturition. Biol Reprod. 1999; 61 797-801
- 56 Schuler G, Wirth C, Klisch K, Failing K, Hoffmann B. Characterization of proliferative activity in bovine placentomes between day 150 and parturition by quantitative immunohistochemical detection of Ki67-antigen. Reprod Dom Anim. 2000; 35 157-162
- 57 Schuler G, Wirth C, Teichmann U, Failing K, Leiser R, Thole H, Hoffmann B. Occurrence of estrogen receptor alpha in bovine placentomes throughout mid and late gestation and at parturition. Biol Reprod. 2002; 66 976-982
- 58 Schuler G, Teichmann U, Taubert A, Failing K, Hoffmann B. Estrogen receptor beta (ERbeta) is expressed differently from ERalpha in bovine placentomes. Exp Clin Endocrinol Diabetes. 2005; 113 107-114
- 59 Schuler G, Ozalp GR, Hoffmann B, Harada N, Browne P, Conley AJ. Reciprocal expression of 17alpha-hydroxylase-C17,20-lyase and aromatase cytochrome P450 during bovine trophoblast differentiation: a two-cell system drives placental oestrogen synthesis. Reproduction. 2006; 131 669-679
- 60 Shemesh M. Production and regulation of progesterone in bovine corpus luteum and placenta in mid and late gestation: a personal review. Reprod Fertil Dev. 1990; 2 129-135
- 61 Shemesh M, Hansel W, Strauss 3rd JF. Calcium-dependent, cyclic nucleotide-independent steroidogenesis in the bovine placenta. Proc Natl Acad Sci USA. 1984; 81 6403-6407
- 62 Shemesh M, Harel-Markowitz E, Gurevich M, Shore LS. Staurosporine stimulates progesterone production by bovine placental cells. Biol Reprod. 1994; 51 146-151
- 63 Short RV. Steroids in the follicular fluid and the corpus luteum of the mare. A ‘two-cell typ’ theory of ovarian steroid synthesis. J Endocrinol. 1962; 24 59-63
- 64 Smith CL, O'Malley BW. Coregulator function: a key to understanding tissue specificity of selective receptor modulators. Endocr Rev. 2004; 25 45-71
- 65 Spencer TE, Johnson GA, Burghardt RC, Bazer FW. Progesterone and placental hormone actions on the uterus: insights from domestic animals. Biol Reprod. 2004; 71 2-10
- 66 Strauss 3rd JF, Martinez F, Kiriakidou M. Placental steroid hormone synthesis: unique features and unanswered questions. Biol Reprod. 1996; 54 303-311
- 67 Tsumagari S, Kamata J, Takagi K, Tanemura K, Yosai A, Takeishi M. Aromatase activity and oestrogen concentrations in bovine cotyledons and caruncles during gestation and parturition. J Reprod Fertil. 1993; 98 631-636
- 68 Tsumagari S, Kamata J, Takagi K, Tanemura K, Yosai A, Takeishi M. 3ß-Hydroxysteroid dehydrogenase activity and gestagen concentrations in bovine cotyledons and caruncles during gestation and parturition. J Reprod Fertil. 1994; 102 35-39
- 69 Ushizawa K, Takahashi T, Hosoe M, Ishiwata H, Kaneyama K, Kizaki K, Hashizume K. Global gene expression analysis and regulation of the principal genes expressed in bovine placenta in relation to the transcription factor AP-2 family. Reprod Biol Endocrinol. 2007; 27 5-17
- 70 Verduzco Gomez A, Miranda L, Murphy B, Quero A. Expression of Steroidogenic Acute Regulatory Protein (StAR) in caruncular and cotyledonary bovine tissues during the first half of the gestation. Biol Reprod. 2007; , Special issue. Abstract book. Society for the Study of Reproduction. 40th Annual Meeting, July 21–July 25, 2007, San Antonio, Texas
- 71 Wildman DE, Chen C, Erez O, Grossman LI, Goodman M, Romero R. Evolution of the mammalian placenta revealed by phylogenetic analysis. Proc Natl Acad Sci USA. 2006; 103 3203-3208
- 72 Woicke J, Schoon HA, Heuwieser W, Schulz LC, Grunert E. Morphological and functional aspects of placental maturing mechanisms in the cow. 1. Light microscopic findings. Zentralbl Veterinärmed A. 1986; 33 660-667
- 73 Wooding FB, Wathes DC. Binucleate cell migration in the bovine placentome. J Reprod Fertil. 1980; 59 425-430
- 74 Zhu BT, Han GZ, Shim JY, Wen Y, Jiang XR. Quantitative structure-activity relationship of various endogenous estrogen metabolites for human estrogen receptor alpha and beta subtypes: Insights into the structural determinants favoring a differential subtype binding. Endocrinology. 2006; 147 4132-4150
Correspondence
Dr. G. Schuler
Clinic for Obstetrics
Gynecology & Andrology of Large and Small Animals
Faculty of Veterinary Medicine
Justus-Liebig-University
35392 Giessen
Germany
Telefon: +64/199/38 71 8
Fax: +64/199/38 70 9
eMail: Gerhard.Schuler@vetmed.uni-giessen.de