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Normal human endometrium in cell culture
Authors:D Kirk  R J B King  Judy Heyes  Linda Peachey  P J Hirsch  R W T Taylor
Institution:(1) Department of Hormone Biochemistry, Lincoln's Inn Fields, WC2A 3PX London;(2) Department of Pathology, Imperial Cancer Research Fund, Lincoln's Inn Fields, WC2A 3PX London;(3) Hope Hospital, Eccles Old Road, M6 8HD Salford;(4) Department of Obstetrics and Gynaecology, St. Thomas' Hospital, SE1 7EH London
Abstract:Summary Separation of human endometrium into its epithelial and stromal components has been achieved through collagenase digestion and has permitted a study of these two cell populations under specific experimental culture conditions. The stromal cell populations showed a progesterone response, were easily handled in culture, and displayed a limited in vitro life span typical of human diploid fibroblasts. In contrast, epithelium only survived in shortterm primary culture and showed no clear hormone response. High-density epithelial cultures remained viable for longer periods in culture. Comparisons between resurfacing endometrial epithelial cells in vivo and epithelial cells migrating from explants in vitro suggested that this initial epithelial migration in vitro was the counterpart of the repair response in vivo. We are much in debt to Dr. R. C. Hallowes (Department of Pathology, Imperial Cancer Research Fund) for his guidance and encouragement throughout the course of this work. We also gratefully acknowledge Dr. P. N. Riddle (Time-Lapse Cinematography Unit, Imperial Cancer Research Fund) for carrying out the time-lapse cinematography; Mrs. Lyn Rolph (Stereoscan Unit, Bedford College, University of London) for assisting with the SEM; and Mr. G. D. Leach for his competent help with the photography.
Keywords:cell culture  human endometrium  epithelium  stroma
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