Literature DB >> 8439617

Localization of leukocyte subsets in the rat ovary during the periovulatory period.

M Brännström1, G Mayrhofer, S A Robertson.   

Abstract

The ovulatory process has been compared with inflammation because several classical inflammatory mediators appear to participate in this process. One component of the inflammatory reaction is the migration of leukocytes to the site of inflammation and the subsequent activation of these cells. We have reported recently that perfusion of leukocytes into the rat ovary in vitro enhances the number of LH-induced ovulations, which suggests an active role of leukocytes in ovulation. In the present study we characterize immunohistochemically the distribution of macrophages, T lymphocytes, and granulocytes in the ovaries of untreated immature rats and of eCG-hCG-primed rats killed prior to hCG injection, at ovulation, and at 33-36 h post-ovulation. Macrophages, identified with monoclonal antibodies ED1 and ED2, were the major leukocyte population and were found primarily in the medullary region surrounding the blood vessels. The density of the cells in this region increased continuously during development to sexual maturity and until after ovulation. Macrophages were also present in the thecal layer of the preovulatory follicles, and the numbers of these cells increased about 5-fold in this area in ovulating follicles (12 h after hCG) compared to preovulatory follicles (before hCG). A portion of macrophages in both areas expressed major histocompatibility complex (MHC) class II antigens (OX6+); these cells were present mostly in the medullary region, with no apparent change in density during the periovulatory period. Neutrophilic granulocytes comprised a lesser proportion of the total leukocyte population in the medullary region but were abundant in the thecal layer. The density of neutrophils increased 3-fold in the medullary region and 8-fold in the thecal region in ovulatory compared to preovulatory follicles. T lymphocytes (OX52+) were evenly distributed at relatively low density in the medulla and the stroma of the cortex. Most T lymphocytes expressed the CD8 antigen (OX8+) and hence were of the MHC class I-restricted phenotype. Few T lymphocytes were present in the thecal layer. In summary, macrophages, neutrophilic granulocytes, and T lymphocytes are present in the ovary at ovulation. There is a selective increase in the numbers of macrophages and neutrophilic granulocytes in the medullary region and in the thecal layer as the ovulatory period progresses, indicating that these cells may actively be involved in the tissue remodeling occurring at ovulation.

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Year:  1993        PMID: 8439617     DOI: 10.1095/biolreprod48.2.277

Source DB:  PubMed          Journal:  Biol Reprod        ISSN: 0006-3363            Impact factor:   4.285


  40 in total

1.  Occurrence of immunoreactivity for adipocyte-type fatty acid binding protein in degenerating granulosa cells in atretic antral follicles of mouse ovary.

Authors:  Mohammad Reza Nourani; Yuji Owada; Noriko Kitanaka; Hiroyuki Sakagami; Hisae Hoshi; Hiroo Iwasa; Friedrich Spener; Hisatake Kondo
Journal:  J Mol Histol       Date:  2006-04-28       Impact factor: 2.611

2.  Female mice with loss-of-function ITCH display an altered reproductive phenotype.

Authors:  Angela R Stermer; Jessica L Myers; Caitlin J Murphy; Kristin R Di Bona; Lydia Matesic; John H Richburg
Journal:  Exp Biol Med (Maywood)       Date:  2015-10-28

3.  Periovulatory leukocyte infiltration in the rat ovary.

Authors:  Oliver R Oakley; HeyYoung Kim; Ismail El-Amouri; Po-Ching Patrick Lin; Jongki Cho; Mohammad Bani-Ahmad; Chemyong Ko
Journal:  Endocrinology       Date:  2010-06-30       Impact factor: 4.736

4.  Unique temporal and spatial expression patterns of IL-33 in ovaries during ovulation and estrous cycle are associated with ovarian tissue homeostasis.

Authors:  Colin I Carlock; Jean Wu; Cindy Zhou; Kiana Tatum; Henry P Adams; Filemon Tan; Yahuan Lou
Journal:  J Immunol       Date:  2014-05-23       Impact factor: 5.422

Review 5.  Ovulation: Parallels With Inflammatory Processes.

Authors:  Diane M Duffy; CheMyong Ko; Misung Jo; Mats Brannstrom; Thomas E Curry
Journal:  Endocr Rev       Date:  2019-04-01       Impact factor: 19.871

6.  Pituitary-ovary-spleen axis in ovulation.

Authors:  Oliver R Oakley; Michele L Frazer; CheMyong Ko
Journal:  Trends Endocrinol Metab       Date:  2011-05-18       Impact factor: 12.015

7.  Reactive oxygen species are indispensable in ovulation.

Authors:  Ketty Shkolnik; Ari Tadmor; Shifra Ben-Dor; Nava Nevo; Dalia Galiani; Nava Dekel
Journal:  Proc Natl Acad Sci U S A       Date:  2011-01-10       Impact factor: 11.205

8.  Chemokine Ligand 20: A Signal for Leukocyte Recruitment During Human Ovulation?

Authors:  Linah Al-Alem; Muraly Puttabyatappa; Kathy Rosewell; Mats Brännström; James Akin; Jeffrey Boldt; Ken Muse; Thomas E Curry
Journal:  Endocrinology       Date:  2015-06-30       Impact factor: 4.736

9.  Macrophages regulate corpus luteum development during embryo implantation in mice.

Authors:  Alison S Care; Kerrilyn R Diener; Melinda J Jasper; Hannah M Brown; Wendy V Ingman; Sarah A Robertson
Journal:  J Clin Invest       Date:  2013-07-08       Impact factor: 14.808

10.  Potential roles of a special CD8 alpha alpha+ cell population and CC chemokine thymus-expressed chemokine in ovulation related inflammation.

Authors:  Cindy Zhou; Jean Wu; Jason Borillo; Lisa Torres; John McMahon; Ya-Huan Lou
Journal:  J Immunol       Date:  2009-01-01       Impact factor: 5.422

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