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BOR - Papers in Press, published online ahead of print January 19, 2005.
Biol Reprod 2005, 10.1095/biolreprod.104.032953
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BIOLOGY OF REPRODUCTION 72, 1169–1176 (2005)
DOI: 10.1095/biolreprod.104.032953
© 2005 by the Society for the Study of Reproduction, Inc.

Cooperative Expression of Monocyte Chemoattractant Protein 1 Within the Bovine Corpus Luteum: Evidence of Immune Cell-Endothelial Cell Interactions in a Coculture System1

Amy R. Liptak 3, Brian T. Sullivan 3, Luiz E. Henkes 4, Missaka P.B. Wijayagunawardane 5, Akio Miyamoto 6, John S. Davis 7, Bo R. Rueda 4, and David H. Townson 2 3

Department of Animal and Nutritional Sciences,3 University of New Hampshire, Durham, New Hampshire 03824 Vincent Center for Reproductive Biology,4 Massachusetts General Hospital/Harvard Medical School, Boston, Massachusetts 02114 Department of Animal Science,5 University of Peradeniya, Peradeniya 20400, Sri Lanka Department of Agricultural and Life Science,6 Obihiro University of Agriculture and Veterinary Medicine, Obihiro 080-8555, Japan Department of Obstetrics and Gynecology,7 University Nebraska Medical Center and Veterans Affairs Medical Center, Omaha, Nebraska 68198

Endothelial cells (EC) of the bovine corpus luteum (CL) are a known source of proinflammatory mediators, including monocyte chemoattractant protein 1 (CCL2) and endothelin 1 (EDN1). Here, a coculture system was devised to determine if immune cells and PGF2{alpha} together affect CCL2 and EDN1 secretion by EC. Luteal EC were cultured either alone or together with peripheral blood mononuclear cells (PBMC), and treated without or with PGF2{alpha} for 48 h (n = 6 experiments). Coculture of EC with PBMC increased CCL2 secretion an average of 5-fold higher compared with either cell type alone (P < 0.05). Basal secretion of EDN1 by EC was substantial (~2 ng/ml), but was not affected by coculture with PBMC (P > 0.05). EC cocultured with concanavalin A-activated PBMC (ActPBMC) increased CCL2 secretion an average of 12-fold higher compared with controls (P < 0.05), but again, EDN1 secretion was unchanged (P > 0.05). Interestingly, PGF2{alpha} did not alter either CCL2 or EDN1 secretion, regardless of culture conditions (P > 0.05). In a second series of experiments (n = 3 experiments), mixed luteal cells (MLC) were cultured alone or with PBMC as described above. Secretion of CCL2 and EDN1 was not affected by coculture or by PGF2{alpha} (P > 0.05), but MLC produced less progesterone in the presence of ActPBMC (P < 0.05). Collectively, these results suggest that immune cells and EC can interact cooperatively to increase CCL2 secretion in the CL, but this interaction does not affect EDN1 secretion nor is it influenced by PGF2{alpha}. Additionally, activated immune cells appear to produce a factor that impairs progesterone production by luteal steroidogenic cells.

corpus luteum, corpus luteum function, cytokines, immunology, progesterone


1 This is scientific contribution 2238 from the New Hampshire Agricultural Experiment Station. The work was supported by USDA grant 2002-35203-12257, NIH HD35934, and the VA.

2 Correspondence: David Townson, 509 Kendall Hall, Durham, NH 03824-3590 FAX: 603 862 3758; dave.townson{at}unh.edu




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