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Effect of high concentrations of glucose on differentiation of rat trophoblast cells in vitro.

Bibliographic reference Hinck, Laurence ; Thissen, Jean-Paul ; Pampfer, S. ; De Hertogh, René. Effect of high concentrations of glucose on differentiation of rat trophoblast cells in vitro.. In: Diabetologia, Vol. 46, no. 2, p. 276-83 (2003)
Permanent URL http://hdl.handle.net/2078.1/22021
  1. Gardner RL, Papaioannou VE, Barton S-C (1973) Origin of the ectoplacental cone and secondary giant cells in mouse blastocysts reconstituted from isolated trophoblast and inner cell mass. J Embryol Exp Morph 30:561–572
  2. Barlow Peter W., Sherman Michael I., Cytological studies on the organization of DNA in giant trophoblast nuclei of the mouse and the rat, 10.1007/bf00331800
  3. Bower D. Jane, Chromosome organisation in polyploid mouse trophoblast nuclei, 10.1007/bf00293845
  4. Ilgren E.B., Control of trophoblastic growth, 10.1016/s0143-4004(83)80010-1
  5. Carney E. W., Prideaux V., Lye S. J., Rossant J., Progressive expression of trophoblast-specific genes during formation of mouse trophoblast giant cells in vitro, 10.1002/mrd.1080340403
  6. Strickland Sidney, Richards William G., Invasion of the trophoblasts, 10.1016/0092-8674(92)90503-5
  7. Desoye G, Shafrir E (1996) The human placenta in diabetic pregnancy. Diabetes Rev 4:70–89
  8. Gewolb I. H., Merdian W., Warshaw J. B., Enders A. C., Fine Structural Abnormalities of the Placenta in Diabetic Rats, 10.2337/diab.35.11.1254
  9. Leunda-Casi Amaya, de Hertogh Ren�, Pampfer Serge, Control of trophectoderm differentiation by inner cell mass-derived fibroblast growth factor-4 in mouse blastocysts and corrective effect of fgf-4 on high glucose-induced trophoblast disruption, 10.1002/mrd.1059
  10. Caluwaerts S., Pijnenborg R., Luyten C., Van Assche F. A., Growth characteristics of diabetic rat ectoplacental cones in vivo and in vitro, 10.1007/s001250051473
  11. Pampfer S., Wuu Y. D., Vanderheyden I., Hertogh R. De, In vitro study of the carry-over effect associated with early diabetic embryopathy in the rat, 10.1007/s001250050188
  12. Pampfer S, De Hertogh R (1996) Preimplantation embryopathy associated with maternal diabetes. Diabetes Rev 4:90–113
  13. Peters TJ, Chapman BM, Soares MJ (1998) Trophoblast differentiation: an in vitro model for trophoblast giant cell development. In: Tuan RS, Lo CW (eds) Methods in molecular biology, 137. Humana Press, Totowa, pp 301–311
  14. Hamlin G P, Lu X J, Roby K F, Soares M J, Recapitulation of the pathway for trophoblast giant cell differentiation in vitro: stage-specific expression of members of the prolactin gene family., 10.1210/endo.134.6.8194465
  15. Dai G, Imagawa W, Liu B, Szpirer C, Levan G, Kwok S C, Soares M J, Rcho-1 trophoblast cell placental lactogens: complementary deoxyribonucleic acids, heterologous expression, and biological activities., 10.1210/endo.137.11.8895376
  16. FARIA TERESA N., SOARES MICHAEL J., Trophoblast Cell Differentiation: Establishment, Characterization, and Modulation of a Rat Trophoblast Cell Line Expressing Members of the Placental Prolactin Family*, 10.1210/endo-129-6-2895
  17. Soares M.J., Chapman B.M., Rasmussen C.A., Dai G., Kamei T., Orwig K.E., Differentiation of trophoblast endocrine cells, 10.1016/s0143-4004(96)90051-x
  18. Moley K.H., Chi M.M.-Y., Knudson C.M., Korsmeyer S.J., Mueckler M.M., Hyperglycemia induces apoptosis in pre-implantation embryos through cell death effector pathways, 10.1038/4013
  19. Pampfer S, Vanderheyden I, McCracken JE, Vesela J, De Hertogh R (1997) Increased cell death in rat blastocysts exposed to maternal diabetes in utero and to high glucose or tumor necrosis factor-α in vitro. Development 124:4827–4836
  20. Pampfer S., Apoptosis in Rodent Peri-implantation Embryos: Differential Susceptibility of Inner Cell Mass and Trophectoderm Cell Lineages— A Review, 10.1053/plac.1999.0519
  21. Weiss U., Cervar M., Puerstner P., Schmut O., Haas J., Mauschitz R., Arikan G., Desoye G., Hyperglycaemia in vitro alters the proliferation and mitochondrial activity of the choriocarcinoma cell lines BeWo, JAR and JEG-3 as models for human first-trimester trophoblast, 10.1007/s001250051601
  22. Zybina EV (1970) Charasteristics of polyploidization of trophoblast cells. Tsitologiia 12:1081–1094
  23. Hoffman Loren H., Wooding F. B. P., Giant and binucleate trophoblast cells of mammals, 10.1002/jez.1402660607
  24. Zybina Eugenia V., Zybina Tatiana G., Polytene Chromosomes in Mammalian Cells, International Review of Cytology (1996) ISBN:9780123645692 p.53-119, 10.1016/s0074-7696(08)62220-2
  25. Varmuza S, Prideaux V, Kothary R, Rossant J (1988) Polytene chromosomes in mouse trophoblast giant cells. Development 102:127–134
  26. MacAuley A., Cross J. C., Werb Z., Reprogramming the Cell Cycle for Endoreduplication in Rodent Trophoblast Cells, 10.1091/mbc.9.4.795
  27. Hattori N., Davies T. C., Anson-Cartwright L., Cross J. C., Periodic Expression of the Cyclin-dependent Kinase Inhibitor p57Kip2 in Trophoblast Giant Cells Defines a G2-like Gap Phase of the Endocycle, 10.1091/mbc.11.3.1037
  28. Padmanabhan R, al-Zuhair A (1990) Ultrastructural studies on the placentae of streptozotocin induced maternal diabetes in the rat. Z Mikrusk Anat Forsch 104:212–230
  29. Prager R., Abramovici A., Liban E., Laron Z., Histopathological changes in the placenta of streptozotocin induced diabetic rats, 10.1007/bf00421419
  30. Robinson J., Canavan J. P., El Haj A. J., Goldspink D. F., Maternal Diabetes in Rats: I. Effects on Placental Growth and Protein Turnover, 10.2337/diab.37.12.1665
  31. Husain Shahid M., Frost Rachel, Mughal Zulf M., Effect of diabetes mellitus on rat placenta cellularity, 10.1016/s0378-3782(00)00119-5
  32. Diamant Y.Z., Metzger B.E., Freinkel N., Shafrir E., Placental lipid and glycogen content in human and experimental diabetes mellitus, 10.1016/0002-9378(82)90385-4
  33. Gewolb Ira H, Barrett Carolyn, Warshaw Joseph B, Placental Growth and Glycogen Metabolism in Streptozotocin Diabetic Rats, 10.1203/00006450-198307000-00014
  34. Peters T. J., Albieri Andrea, Bevilacqua Estela, Chapman Belinda M., Crane L. H., Hamlin G. P., Seiki Motoharu, Soares M. J., Differentiation-dependent expression of gelatinase B/matrix metalloproteinase-9 in trophoblast cells, 10.1007/s004410051235
  35. Alexander CM, Hansell EJ, Behrendtsen O et al. (1996) Expression and function of matrix metalloproteinases and their inhibitors at the maternal-embryonic boundary during mouse embryo implantation. Development 122:1723–1736
  36. Das Sanjoy K., Yano Shojiro, Wang Jue, Edwards Dylan R., Nagase Hideaki, Dey Sudhansu K., Expression of matrix metalloproteinases and tissue inhibitors of metalloproteinases in the mouse uterus during the peri-implantation period, 10.1002/(sici)1520-6408(1997)21:1<44::aid-dvg5>3.0.co;2-8
  37. Pustovrh Carolina, Jawerbaum Alicia, Sinner Debora, Pesaresi Mario, Baier Mario, Micone Paula, Gimeno Martha, Gonzalez Elida T., Membrane-type matrix metalloproteinase-9 activity in placental tissue from patients with pre-existing and gestational diabetes mellitus, 10.1071/rd00078
  38. Harvey M.B., Leco K.J., Arcellana-Panlilio M.Y., Zhang X., Edwards D.R., Schultz G.A., Endocrinology and paracrinology: Roles of growth factors during peri-implantation development, 10.1093/oxfordjournals.humrep.a136021
  39. Sharma RK (1998) Mouse trophoblastic cell lines: II. Relationship between invasive potential and proteases. In Vivo 12:209–217
  40. Teesalu Tambet, Masson R�gis, Basset Paul, Blasi Francesco, Talarico Daniela, Expression of matrix metalloproteinases during murine chorioallantoic placenta maturation, 10.1002/(sici)1097-0177(199903)214:3<248::aid-aja8>3.0.co;2-n
  41. Waterhouse Paul, Denhardt David T., Khokha Rama, Temporal expression of tissue inhibitors of metalloproteinases in mouse reproductive tissues during gestation, 10.1002/mrd.1080350302
  42. Reis Fernando M., D’Antona Donato, Petraglia Felice, Predictive Value of Hormone Measurements in Maternal and Fetal Complications of Pregnancy, 10.1210/edrv.23.2.0459
  43. Yamaguchi M., Ogren L., Endo H., Soares M. J., Talamantes F., Co-Localization of Placental Lactogen-I, Placental Lactogen-II, and Proliferin in the Mouse Placenta at Midpregnancy1, 10.1095/biolreprod51.6.1188
  44. Selenkow H. A., Varma K., Younger D., White P., Emerson K., Patterns of Serum Immunoreactive Human Placental Lactogen (IR-HPL) and Chorionic Gonadotropin (IR-HCG) in Diabetic Pregnancy, 10.2337/diab.20.10.696
  45. Pedersen JanFog, Søorensen Steen, Mølsted-Pedersen Lars, Serum levels of human placental lactogen, pregnancy-associated plasma protein A and endometrial secretory protein PP14 in first trimester of diabetic pregnancy, 10.1080/j.1600-0412.1998.770204.x
  46. MILLS N, GYVES M, ILAN J, Comparisons of human placental lactogen mRNA levels from placentas of diabetics and normal term, 10.1016/0303-7207(85)90092-9
  47. Soares M. J., Glasser S. R., Placental lactogen production and functional differentiation of rat trophoblast cells in vitro, 10.1530/jrf.0.0790335
  48. Siiteri Pentti K., Stites Daniel P., Immunologic and Endocrine Interrelationships in Pregnancy, 10.1095/biolreprod26.1.1
  49. Thellin Olivier, Coumans Bernard, Zorzi Willy, Igout Ahmed, Heinen Ernst, Tolerance to the foeto-placental ‘graft’: ten ways to support a child for nine months, 10.1016/s0952-7915(00)00170-9
  50. Piccinni M, Role of hormone-controlled Th1- and Th2-type cytokines in successful pregnancy, 10.1016/s0165-5728(00)00299-x
  51. Ben-Zimra M, Koler M, Melamed-Book N, Arensburg J, Payne AH, Orly J (2002) Uterine and placental expression of steroidogenic genes during rodent pregnancy Mol Cell Endocrinol 187:223–231