Ultrastructural alterations in human decidua in miscarriages compared to normal pregnancy decidua

References

• Dietl J, Ruck P, Horny HP, Handgretinger R, Marzusch K, Ruck M, et al. The decidua of early human pregnancy: immunohistochemistry and function of immunocompetent cells. Gynecol Obstet Invest. 1992; 33(4)197–204
   PubMed Web of Science ®Google Scholar
• Demir R, Kayisli UA, Celik-Ozenci C, Korgun ET, Demir-Weusten AY, Arici A. Structural differentiation of human uterine luminal and glandular epithelium during early pregnancy: an ultrastructural and immunohistochemical study. Placenta. 2002; 23(8–9)672–84
   PubMed Web of Science ®Google Scholar
• Mikhailov VM. Life cycle of decidual cells. Int Rev Cytol. 2003; 227: 1–63
   PubMedGoogle Scholar
• Can A, Tekelioglu M, Biberoglu K. Structure of premenstrual endometrium in HMG + HCG induced anovulatory women. Eur J Obstet Gynecol Reprod Biol. 1991; 42(2)119–29
   PubMed Web of Science ®Google Scholar
• Wewer UM, Faber M, Liotta LA, Albrechtsen R. Immunochemical and ultrastructural assessment of the nature of the pericellular basement membrane of human decidual cells. Lab Invest. 1985; 53(6)624–33
   PubMed Web of Science ®Google Scholar
• Parr MB, Tung HN, Parr EL. The ultrastructure of the rat primary decidual zone. Am J Anat. 1986; 176(4)423–36
   PubMedGoogle Scholar
• Wynn RM. Ultrastructural development of the human decidua. Am J Obstet Gynecol. 1974; 118(5)652–70
   PubMed Web of Science ®Google Scholar
• Pakurar AS, Bigbee JW. Digital histology. Wiley-Liss, New Jersey 2004
   Google Scholar
• Tabanelli S, Tang B, Gurpide E. In vitro decidualization of human endometrial stromal cells. J Steroid Biochem Mol Biol. 1992; 42(3–4)337–44
   PubMed Web of Science ®Google Scholar
• Edwards GE. Conception in the human female. Academic Press, London 1980
   Google Scholar
• Tekelioglu-Uysal M, Edwards RG, Kisnisci HA. Ultrastructural relationships between decidua, trophoblast and lymphocytes at the beginning of human pregnancy. J Reprod Fertil. 1975; 42(3)431–8
   PubMedGoogle Scholar
• Herr JC, Heidger PM, Jr, Scott JR, Anderson JW, Curet LB, Mossman HW. Decidual cells in the human ovary at term. I. Incidence, gross anatomy and ultrastructural features of merocrine secretion. Am J Anat. 1978; 152(1)7–27
   PubMedGoogle Scholar
• Bulmer JN. Histopathological changes in decidua in human spontaneous abortion. Am J Reprod Immunol Microbiol. 1987; 14(4)144–6
   PubMedGoogle Scholar
• King A, Wooding P, Gardner L, Loke YW. Expression of perforin, granzyme A and TIA-1 by human uterine CD56+ NK cells implies they are activated and capable of effector functions. Hum Reprod. 1993; 8(12)2061–7
   PubMed Web of Science ®Google Scholar
• King A, Loke YW. On the nature and function of human uterine granular lymphocytes. Immunol Today. 1991; 12(12)432–5
   PubMedGoogle Scholar
• Scott JR, DiSaia PJ, Hammond CB, Spellacy WN. Danforth's obstetrics and gynecology7th edn. JB Lippincott Co, Philadelphia 1994
   Google Scholar
• Li TC, Iqbal T, Anstie B, Gillham J, Amer S, Wood K, et al. An analysis of the pattern of pregnancy loss in women with recurrent miscarriage. Fertil Steril. 2002; 78(5)1100–6
   PubMed Web of Science ®Google Scholar
• Vassiliadou N, Bulmer JN. Characterization of endometrial T lymphocyte subpopulations in spontaneous early pregnancy loss. Hum Reprod. 1998; 13(1)44–7
   PubMed Web of Science ®Google Scholar
• Vassiliadou N, Bulmer JN. Functional studies of human decidua in spontaneous early pregnancy loss: effect of soluble factors and purified CD56+ lymphocytes on killing of natural killer- and lymphokine-activated killer-sensitive targets. Biol Reprod. 1998; 58(4)982–7
   PubMed Web of Science ®Google Scholar
• Beer AE, Kwak JY, Ruiz JE. Immunophenotypic profiles of peripheral blood lymphocytes in women with recurrent pregnancy losses and in infertile women with multiple failed in vitro fertilization cycles. Am J Reprod Immunol. 1996; 35(4)376–82
   PubMed Web of Science ®Google Scholar
• Dosiou C, Giudice L. Natural killer cells in pregnancy and recurrent pregnancy loss: endocrine and immunologic perspectives. Endocrine Rev. 2003; 26(1)44–62
   Web of Science ®Google Scholar
• Psychoyos A. Uterine receptivity for nidation. Ann NY Acad Sci. 1986; 476: 36–42
   PubMed Web of Science ®Google Scholar
• Cinar O, Semiz O, Can A. A microscopic survey on the efficiency of well-known routine chemical fixatives on cryosections. Acta Histochem. 2006; 108(6)487–96
   PubMed Web of Science ®Google Scholar
• Garris DR, Garris BL. Cytomorphometric analysis and surface ultrastructure of developing decidua. Tissue Cell. 2003; 35(4)233–42
   PubMed Web of Science ®Google Scholar
• Hempstock J, Cindrova-Davies T, Jauniaux E, Burton GJ. Endometrial glands as a source of nutrients, growth factors and cytokines during the first trimester of human pregnancy: a morphological and immunohistochemical study. Reprod Biol Endocrinol. 2004; 2: 58
   PubMedGoogle Scholar
• Kisalus LL, Nunley WC, Herr JC. Protein synthesis and secretion in human decidua of early pregnancy. Biol Reprod. 1987; 36(3)785–98
   PubMed Web of Science ®Google Scholar
• Ritson A, Bulmer JN. Endometrial granulocytes in human decidua react with a natural-killer (NK) cell marker, NKH1. Immunology. 1987; 62(2)329–31
   PubMed Web of Science ®Google Scholar
• Starkey PM, Sargent IL, Redman CW. Cell populations in human early pregnancy decidua: characterization and isolation of large granular lymphocytes by flow cytometry. Immunology. 1988; 65(1)129–34
   PubMed Web of Science ®Google Scholar
• King A, Birkby C, Loke YW. Early human decidual cells exhibit NK activity against the K562 cell line but not against first trimester trophoblast. Cell Immunol. 1989; 118(2)337–44
   PubMed Web of Science ®Google Scholar
• Pace D, Morrison L, Bulmer JN. Proliferative activity in endometrial stromal granulocytes throughout menstrual cycle and early pregnancy. J Clin Pathol. 1989; 42(1)35–9
   PubMed Web of Science ®Google Scholar
• Kodama T, Hara T, Okamoto E, Kusunoki Y, Ohama K. Characteristic changes of large granular lymphocytes that strongly express CD56 in endometrium during the menstrual cycle and early pregnancy. Hum Reprod. 1998; 13(4)1036–43
   PubMed Web of Science ®Google Scholar
• Bulmer J, Morrison L, Longfellow M, Ritson A, Pace D. Granulated lymphocytes in human endometrium: histochemical and immunohistochemical studies. Hum Reprod. 1991; 6: 791–8
   PubMed Web of Science ®Google Scholar
• Starkey PM, Clover LM, Rees MC. Variation during the menstrual cycle of immune cell populations in human endometrium. Eur J Obstet Gynecol Reprod Biol. 1991; 39(3)203–7
   PubMed Web of Science ®Google Scholar
• Vassiliadou N, Bulmer JN. Quantitative analysis of T lymphocyte subsets in pregnant and nonpregnant human endometrium. Biol Reprod. 1996; 55(5)1017–22
   PubMed Web of Science ®Google Scholar
• Verma S, King A, Loke YW. Expression of killer cell inhibitory receptors on human uterine natural killer cells. Eur J Immunol. 1997; 27(4)979–83
   PubMed Web of Science ®Google Scholar
• Yamamoto T, Takahashi Y, Kase N, Mori H. Decidual natural killer cells in recurrent spontaneous abortion with normal chromosomal content. Am J Reprod Immunol. 1999; 41(5)337–42
   PubMed Web of Science ®Google Scholar
• Yamamoto T, Takahashi Y, Kase N, Mori H. Role of decidual natural killer (NK) cells in patients with missed abortion: differences between cases with normal and abnormal chromosome. Clin Exp Immunol. 1999; 116(3)449–52
   PubMed Web of Science ®Google Scholar
• Vassiliadou N, Bulmer JN. Immunohistochemical evidence for increased numbers of ‘classic’ CD57+ natural killer cells in the endometrium of women suffering spontaneous early pregnancy loss. Hum Reprod. 1996; 11(7)1569–74
   PubMed Web of Science ®Google Scholar
• Lachapelle MH, Miron P, Hemmings R, Roy DC. Endometrial T, B, and NK cells in patients with recurrent spontaneous abortion. Altered profile and pregnancy outcome. J Immunol. 1996; 156(10)4027–34
   PubMed Web of Science ®Google Scholar
• Dosiou C, Giudice LC. Natural killer cells in pregnancy and recurrent pregnancy loss: endocrine and immunologic perspectives. Endocr Rev. 2005; 26(1)44–62
   PubMed Web of Science ®Google Scholar
• Shimada S, Kato EH, Morikawa M, Iwabuchi K, Nishida R, Kishi R, et al. No difference in natural killer or natural killer T-cell population, but aberrant T-helper cell population in the endometrium of women with repeated miscarriage. Hum Reprod. 2004; 19(4)1018–24
   PubMed Web of Science ®Google Scholar
• Shimada S, Nishida R, Takeda M, Iwabuchi K, Kishi R, Onoe K, et al. Natural killer, natural killer T, helper and cytotoxic T cells in the decidua from sporadic miscarriage. Am J Reprod Immunol. 2006; 56(3)193–200
   PubMed Web of Science ®Google Scholar