2002, Number 4
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Perinatol Reprod Hum 2002; 16 (4)
El líquido peritoneal de mujeres con endometriosis promueve la adhesión celular. Modelo in vitro
Hernández-Guerrero C, Vadillo OF, Jiménez-Zamudio L, Tlapanco-Barba R, González-Jiménez M, Ramos-Pérez C, Julio de la Jara-Díaz
Language: Spanish
References: 27
Page: 163-171
PDF size: 266.53 Kb.
ABSTRACT
Objective; To evaluate adhesion cellular capacity of the peritoneal fluid from women with endometriosis.
Material and methods: Seventy percent ethanol and ice were used to denudated amniotic membrane epithelia cells, from human chorioamnios membranes obtained by delivery at term. Wish (amniotic derivate epithelial cell line) cells were used to assignment cellular adhesion; cells were target with 100 mCi/mmol thymidine (
3H) pulse. Around 3 x10
5 target cells were added to a 10 mm amnion explants diameter by 60 minutes, at optimal culture cell conditions, measuring cell adhesion every 10 minutes.
Results: Cell adhesion in an
in vitro model was determined by beta-radioactive measures at the explants. Basal cellular adhesion start at the first ten minutes until sixty minutes, that shows around 5% media cellular adhesion at every kinetic step. Cells incubated whit peritoneal fluid (PF) from endometriosis womwn, shows cellular adhesion increment at all kinetic steps (ANOVA F =30.0; IC 95%, p ‹ 0.05)
versus value showed by control womwn LP, or fetal bovine sera used at the same protein concentration.
Conclusions: Work present here describes an
in vitro model to evaluate cell adhesion; and shows different capacity between LP from endometriosis sterile and fertile women to promotes cell adhesion.
REFERENCES
Prentice A. Endometriosis. Brit Med J 2001; 323: 93-5.
Dizerega GS, Barber DL, Hodgen GD. Endometriosis: Role of ovarian steroids in initiation, maintenance and suppression. Fertil Steril 1980; 33: 649-53.
Sharpe-Timms K. Endometrial anomalies in women with endometriosis. Ann NY Acad Sci 2001; 943: 131-47.
Ramey JW, Archer DF. Peritoneal fluid: its relevance to the development of endometriosis. Fertil Steril 1993; 60: 1-14.
Blumenkrantz MK, Gallagher N, Bashore RA, Tenchkoff H. Retrograde menstruation in women undergoing chronic peritoneal dialysis. Obstet Gynecol 1981; 57: 667-70.
Halme J, Hammond MG, Hulka JF, Raj SG. retrograde menstruation in healthy women and in patients with endiometriosis. Obstet Gynecol 1984; 64: 151-4.
Zamah NM, Dodson MG, Stephens LC, Buttram VC, Besch PK, Kaufman RH. Transplantation of normal and ectopic human endometrial tissue into athymic mice. Am J Obstet Gynecol 1984; 149: 591-7.
Merrill JA. Endometrial induction of endometriosis across Millipore filters. AM J Obstet Gynecol 1966; 94: 780-9.
Hernández-Guerrero C, Ortega-Vadillo F, Tlapanco-Barba R, Arriaga-Pizano L, Cérbulo-Vázquez A, González-Jiménez M. Alteración de la respuesta inmunológica sistémica en asociación con endometriosis, empleando un modelo de estudio animal. Ginec Obstet Mex 2002; 70: 171-81.
Nasir R, Braun DP, House R, Gebel H, Rotman C, Dmowski P. Basal and stimulated secretion of cytokines by peritoneal macrophages in women with endometriosis. Fertil Steril 1996; 65: 925-9.
Oosterlynck DJ, Cornillie FJ, Ware M. Women with endometriosis show a defect in natural killer activity resulting in a decreased cytotoxicity to autologous endometrium. Fertil Steril 1991; 56: 45-51.
Vigano P, Vercellini P, DiBlasio AM, Colombo A. Deficient antiendometrium lymphocyte-mediated cytotoxicity in patients with endometriosis. Fertil Steril 1991; 56: 894-8.
Oosterlynck DJ, Lacquet FA, Waer M, Koninckx PR. Lymphokine activated killer activity in women with endometriosis. Obstet Gynecol 1994; 37: 185-90.
Erick R. Integrins. J Clin Invest 1991; 87: 1-5.
Nisolle M, Casanas-Roux F, Donnez J. Coexpression of cytokeratin and vimentin in eutopic endometrium and andometriosis througthout the menstrual cycle: evaluation by computerized method. Fertil Steril 1995; 64: 69-75.
Viale G, Gambacorta M, Dell´Orto P, Coggi G. Coexpression of cytokeratins and vimentin in common epithelial tumors of the ovary: an immunocytochemical study of 83 cases. Virchows Arch 1997; 413: 91-101.
Nakopoulou L, Minaretzia D, Tsionou C, Mastrominas, M. Value of immunohistochemical demonstration of several ephitelial markers in hyperplasia and neoplasic endometrium. Gynecol Oncol 1990; 37: 346-53.
Matthews J, Redfern C, Hirst B, Thomas E. Characterization of human purified epithelial and stromal cells from endometrium and endometriotic tissue culture. Fertil Steril 1992; 57: 990-8.
Nissolle M, Donnez J, Casas-Roux R. Expression of steroid receptors, vimentin and cytokeratin in endometiotic tissue. In: H. Minaguchi (ed.). Endometriosis today. kyoto Japan: The Pathenon Publishing Group; 1996.
Parry S, Strauss JF III. Premature rupture of the fetal membranes. New Eng J Med 2000; 338: 663-70.
van der Linden JQ, de Gopeij, FP, Erkens, DA. Expression of cadherins and integrins in human endometrium throughout the menstrual cycle. Fertil Steril 1995; 63: 1210-6.
Mazzeo D, Vigano P, Di Blasio AM, Sinigaglia F, Vignali M, Panina-Bordignon P. interleukin-12 and its free p40 subunit regulate immune recognition of endometrial cells: potential role in endometriosis. J Clin Endocrinol Metab 1998; 83: 911-6.
Keenan JA, Chen TT, Chadwell NL, Torry DS, Caudle MR. IL-1β, TNF-α, and IL-2 in peritoneal fluid and macrophage-conditioned media of women with endometriosis. Am J Reprod Immunol 1995; 34: 381-5.
Ota H, Igarashi S, Hatazawa J, tanaka T. Endometriosis and free radicals. Gynecol Obstet Invest 1999; 481: 29-35.
Iwabe T, Harada T, Tsudo T. Tumor necrosis factor alpha promotes proliferation of endometriotic stromal cells by inducing interleukin-8 gene and protein expression. J Clin Endocrinol Metab 2000; 852: 824-9.
Sillem M, Prifti S, Monga B, Arslic T, Runnebaum B. Integrin mediated adhesion of uterine endometrial cells form endometriosis patients to extracellular matrix proteins is enhanced by tumor necrosis factor alpha (TNF-α) and interleukin-1 (IL-1). Reprod Biol 1999; 872: 123-7.
García-Velasco JA, Arici A, Zreik T, Naftolin F, or G. Macrophage derived growth factors modulate Fas-ligand expression in cultured endometrial stromal cell: a role in endometriosis. Mol Hum Reprod 1999; 57: 642-50.