Biol Reprod Track the topics, authors and articles important to you
HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
 QUICK SEARCH:   [advanced]


     


This Article
Right arrow Full Text (PDF)
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Right arrow Citation Map
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Right arrow reprints & permissions
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Perez, M. C.
Right arrow Articles by Lyttle, C. R.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Perez, M. C.
Right arrow Articles by Lyttle, C. R.
Agricola
Right arrow Articles by Perez, M. C.
Right arrow Articles by Lyttle, C. R.

Biology of Reproduction, Vol 54, 249-254, Copyright © 1996 by Society for the Study of Reproduction


ARTICLES

Role of eosinophils in uterine responses to estrogen

MC Perez, EE Furth, PD Matzumura and CR Lyttle
Department of Obstetrics and Gynecology, University of Pennsylvania School of Medicine, Philadelphia 19104, USA.

Administration of estradiol (E2) to ovariectomized mice results in a dramatic increase in uterine growth and an influx of eosinophilic leukocytes. This influx is mediated by stimulation of an E2-dependent eosinophilic chemotactic factor in the uterus (ECF-U). The role of this eosinophil infiltration in uterus is presently unknown but could involve early growth and/or remodeling processes. In an attempt to better define eosinophil function in uterine tissue, we produced ovariectomized mice severely depleted of circulating eosinophils by administration of a purified rat IgG monoclonal antibody against interleukin-5 (IL-5). Seven days later, animals were submitted to estradiol treatment. Experimental groups included mice treated with saline alone, saline followed by E2, IgG followed by E2, and anti-IL-5 followed by E2. Pretreatment with IL-5 antibodies led to no significant alteration in E2-induced increase in uterine wet weight. However, histological evaluation demonstrated a clear and almost complete blockade of E2-stimulated influx of eosinophils in anti-IL-5 treated animals. In addition, IL-5 antibody administration significantly reduced E2-induced increase in peroxidase activity. Dramatic reduction of eosinophils did not affect E2 stimulation of ECF-U activity by stromal cells or complement C3 synthesis by the epithelial cells. Thus, it appears that differences in E2 responses in eosinophil-deficient mice are not directly associated with presence or absence of eosinophils. Taken together, these data suggest that eosinophils most likely do not contribute to early growth in the E2-stimulated uterus. A possible role in other events such as remodeling remains to be elucidated.


This article has been cited by other articles:


Home page
Physiol. GenomicsHome page
K. C. Fertuck, J. E. Eckel, C. Gennings, and T. R. Zacharewski
Identification of temporal patterns of gene expression in the uteri of immature, ovariectomized mice following exposure to ethynylestradiol
Physiol Genomics, October 17, 2003; 15(2): 127 - 141.
[Abstract] [Full Text] [PDF]


Home page
Mol. Endocrinol.Home page
S. C. Hewitt, B. J. Deroo, K. Hansen, J. Collins, S. Grissom, C. A. Afshari, and K. S. Korach
Estrogen Receptor-Dependent Genomic Responses in the Uterus Mirror the Biphasic Physiological Response to Estrogen
Mol. Endocrinol., October 1, 2003; 17(10): 2070 - 2083.
[Abstract] [Full Text] [PDF]


Home page
J AndrolHome page
H. Chen, P. H. Chow, S. K. Cheng, A. L. M. Cheung, L. Y. L. Cheng, and W.-S. O
Male Genital Tract Antioxidant Enzymes: Their Source, Function in the Female, and Ability to Preserve Sperm DNA Integrity in the Golden Hamster
J Androl, September 1, 2003; 24(5): 704 - 711.
[Abstract] [Full Text] [PDF]


Home page
Exp. Biol. Med.Home page
W. J. Hendry III, D. M. Sheehan, S. A. Khan, and J. V. May
Developing a Laboratory Animal Model for Perinatal Endocrine Disruption: The Hamster Chronicles
Experimental Biology and Medicine, October 1, 2002; 227(9): 709 - 723.
[Abstract] [Full Text] [PDF]


Home page
Exp. Biol. Med.Home page
D. Cracchiolo, J. W. Swick, L. McKiernan, E. Sloan, S. Raina, C. Sloan, and D. L. Wendell
Estrogen-Dependent Growth of a Rat Pituitary Tumor Involves, But Does Not Require, a High Level of Vascular Endothelial Growth Factor
Experimental Biology and Medicine, July 1, 2002; 227(7): 492 - 499.
[Abstract] [Full Text] [PDF]


Home page
EndocrinologyHome page
V. Gouon-Evans and J. W. Pollard
Eotaxin Is Required for Eosinophil Homing into the Stroma of the Pubertal and Cycling Uterus
Endocrinology, October 1, 2001; 142(10): 4515 - 4521.
[Abstract] [Full Text] [PDF]


Home page
EndocrinologyHome page
P. J. Burton, Z. S. Krozowski, and B. J. Waddell
Immunolocalization of 11{beta}-Hydroxysteroid Dehydrogenase Types 1 and 2 in Rat Uterus: Variation Across the Estrous Cycle and Regulation by Estrogen and Progesterone
Endocrinology, January 1, 1998; 139(1): 376 - 382.
[Abstract] [Full Text] [PDF]


Home page
J. Pharmacol. Exp. Ther.Home page
M. I. Rudolph, M. d. l. A. García, M. Sepulveda, E. Brandan, K. Reinicke, S. Nicovani, and L. Villan
Ethodin: Pharmacological Evidence of the Interaction between Smooth Muscle and Mast Cells in the Myometrium
J. Pharmacol. Exp. Ther., July 1, 1997; 282(1): 256 - 261.
[Abstract] [Full Text]




HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
Copyright © 1996 by the Society for the Study of Reproduction.