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RESEARCH |
Department of Animal Sciences, The Ohio State University/Ohio Agricultural Research and Development Center, 1680 Madison Avenue, Wooster, Ohio 44691, USA and 1 Olson Center for Womens Health, Department of Obstetrics and Gynecology, University of Nebraska Medical Center, Omaha, Nebraska 68198, USA and Veterans Affairs Medical Center, Omaha, Nebraska, 68105, USA
Correspondence should be addressed to J L Pate; Email: pate.1{at}osu.edu
Luteal cells express class II major histocompatibility complex (MHC) molecules and can stimulate T lymphocyte proliferation in vitro. However, it is unknown whether luteal cells express the intracellular components necessary to process the peptides presented by class II MHC molecules. The objective of the present study was to examine the expression and regulation of three major class II-associated antigen processing components class II MHC-associated invariant chain (Ii), DM
and DMß in luteal tissue. Corpora lutea were collected early in the estrous cycle, during midcycle and late in the estrous cycle, and at various times following administration of a luteolytic dose of prostaglandin F2
(PGF2
) to the cow. Northern analysis revealed the presence of mRNA encoding each of the class II MHC-associated antigen processing proteins in luteal tissue. Ii mRNA concentrations did not change during the estrous cycle, whereas DM
and DMß mRNA concentrations were highest in midcycle luteal tissue compared with either early or late luteal tissue. Tumor necrosis factor-
(TNF-
) reduced DM
mRNA concentrations in cultured luteal cells in the presence of LH or PGF2
. DM
and DMß mRNA were also present in highly enriched cultures of luteal endothelial (CLENDO) cells, and DM
mRNA concentrations were greater in CLENDO cultures compared with mixed luteal cell cultures. Expression of invariant chain, DM
and DMß genes indicates that cells within the corpus luteum express the minimal requirements to act as functional antigen-presenting cells, and the observation that CLENDO cells are a source of DM
and DMß mRNA indicates that non-immune cells within the corpus luteum may function as antigen-presenting cells.
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