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BOR - Papers in Press, published online ahead of print November 27, 2002.
Biol Reprod 2002, 10.1095/biolreprod.102.009639
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BIOLOGY OF REPRODUCTION 68, 1491–1495 (2003)
DOI: 10.1095/biolreprod.102.009639
© 2003 by the Society for the Study of Reproduction, Inc.


Gamete Biology

Chemokine Receptor Expression in Human Endometrium1

Naciye Mulayim5, Steven F. Palter3,5, Umit A. Kayisli5,6, Levent Senturk4,5, and Aydin Arici2,5

Department of Obstetrics and Gynecology, Division of Reproductive Endocrinology,5 Yale University School of Medicine, New Haven, Connecticut 06520 Department of Histology and Embryology,6 Akdeniz University School of Medicine, 07070 Antalya, Turkey

Chemokines play a role in endometrial physiology and pathology and may affect endometrial receptivity and menstrual shedding. Chemokines exert their effect by binding to their relevant receptors, the expression levels of which may modulate their action. In the present study, we examined the expression of chemokine receptors CXCR1 and CXCR2 (receptors for interleukin-8) and CCR5 (receptor for RANTES [regulated-on-activation, normal-T-cell-expressed and -secreted], macrophage inflammatory protein [MIP]-1{alpha}, and MIP-1ß) in human endometrium. Human endometria (n = 35) were grouped according to the menstrual cycle phase and examined by immunohistochemistry for CXCR1, CXCR2, and CCR5. In both epithelial and stromal cells, CXCR1 and CXCR2 immunoreactivity was detected. Staining was most prominent at the apical and basal aspects of epithelial cells. Intense CCR5 immunostaining was observed in epithelial and stromal compartments throughout the menstrual cycle. Epithelial and stromal staining for CXCR1 reached a peak at the midsecretory phase, during which it was significantly higher than the level of staining during the proliferative phase (P < 0.05). Immunostaining for CXCR2 and CCR5 showed no significant variation across the menstrual cycle. Expression of interleukin-8 and RANTES in endometrium, together with the presence of their receptors, suggests that autocrine and paracrine interactions involving these chemokines may participate in endometrial physiology.

1 Part of this work is from the Ph.D. thesis of U.A.K

2 Correspondence: Aydin Arici, Department of Obstetrics and Gynecology, Division of Reproductive Endocrinology, Yale University School of Medicine, New Haven, CT 06520. FAX: 203 785 7134; aydin.arici{at}yale.edu

3 Current address: Reproductive Medicine and Surgery Center, Plainview, NY 11803

4 Current address: Istanbul University Cerrahpasa School of Medicine Department of Obstetrics and Gynecology, Division of Reproductive Endocrinology Cerrahpasa, Istanbul, Turkey




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