EPITHELIAL-CELLS FROM HUMAN FALLOPIAN-TUBE IN CULTURE

被引:25
作者
HENRIKSEN, T
TANBO, T
ABYHOLM, T
OPPEDAL, BR
CLAUSSEN, OP
HOVIG, T
机构
[1] Department of Obstetrics and Gynaecology, Aker Hospital
[2] Department of Obstetrics and Gynaecology
[3] Institute of Pathology, National Hospital
关键词
Epithelial cells; Fallopian tube; In-vitro fertilization;
D O I
10.1093/oxfordjournals.humrep.a137034
中图分类号
R71 [妇产科学];
学科分类号
100211 ;
摘要
The epithelial cells lining the inner surface of the Fallopian tube influence the reproductive process by both their ciliary and secretory activities. The aim of the present work was to establish a method to culture these cells as a model for more specific studies of their properties. Minor slices of the mucosal ridges were cut and minced extensively using a fine scissor. The resulting pieces were washed once, resuspended in RPMI 1640 with 20% fetal calf serum and seeded in plastic dishes. After 2 days, the medium was replaced with RPMI 1640 containing human albumin, insulin and transferrin. Seven to 10 days later, the cell number had increased 5-8 times in 70% of the cultures. The identity of the cells was assessed after 1-3 weeks in culture. Of the cells, 98% stained positive for the antibody to epithelial cell-specific protein cytokeratin. Electron microscopic studies of the cultures showed epithelial characteristics including cilia, microvUli and intercellular junctions in the form of desmosomes. The cells could be kept in culture for 6-8 weeks. In conclusion, a method to culture epithelial cells from the human Fallopian tube is described. The cells have been identified and they can be kept in culture for 6-8 weeks in quantities sufficient for experimental use. © 1990 Oxford University Press.
引用
收藏
页码:25 / 31
页数:7
相关论文
共 13 条
  • [1] Brandtzaeg P., Rognum T.O., Evaluation of tissue preparation methods and paired immunofluorescence staining for immuno- cytochemistry of lymphomas, Histochem. J., 15, (1983)
  • [2] Brandtzaeg P., Dale I., Fagerhol M.K., Distribution of a formalin-resistant myelomonocyte antigen (LI) in human tissues.I. Comparison with other leucocyte markers by paired immunofluorescence and immunoenzyme staining, Am. J. Pathol., 87, (1987)
  • [3] Chung S.D., Alavi N., Livingston D., Hiller S., Taub M., Characterization of primary rabbit kidney cultures that express proximal tubule functions in a hormonally defined medium, J. Cell Biol., 95, pp. 118-126, (1982)
  • [4] Gandolfi F., Moor R.M., Stimulation of early embryonic development in sheep by co-culture with oviduct epithelial cells, J. Reprod. Fertil., 81, pp. 23-28, (1987)
  • [5] Hammer M., Larsson-Con V., Menstrual cycle enlargement of occlusive tubes after postmenopausal treatment with natural estrogen, Acta Obstet. Gynecol. Scand., 57, pp. 189-196, (1978)
  • [6] Holthofer H., Miettinen A., Letho V.P., Lethonen E., Virtanen I., Expression of vimentin and cytokeratin types of intermediate filament proteins in developing and adult human kidneys, Lab. Invest., 50, pp. 552-559, (1984)
  • [7] Huitfeldt H.S., Brandtzaeg P., Various keratin antibodies produce immunohistochemical staining of human myocardium and myometrium, Histochemistry, 83, pp. 381-389, (1985)
  • [8] Jansen P.S.R., Endocrine response in the fallopian tube, Endocr. Rev., 5, pp. 525-551, (1984)
  • [9] Lippes J., Enders R.G., Pragay D.A., Bartilomew W.R., The collection and analysis of human fallopian tubal fluid, Contraception, 5, (1972)
  • [10] Lippes J., Krasner J., Alfonso L.A., Dacalos E.D., Lucero R., Human oviductal fluid proteins, Fertil. Steril., 36, (1981)