Granulocyte-macrophage colony-stimulating factor (GM-CSF) targets myeloid leukocytes in the uterus during the post-mating inflammatory response in mice

Citation
Sa. Robertson et al., Granulocyte-macrophage colony-stimulating factor (GM-CSF) targets myeloid leukocytes in the uterus during the post-mating inflammatory response in mice, J REPRO IMM, 46(2), 2000, pp. 131-154
Citations number
44
Categorie Soggetti
Immunology
Journal title
JOURNAL OF REPRODUCTIVE IMMUNOLOGY
ISSN journal
01650378 → ACNP
Volume
46
Issue
2
Year of publication
2000
Pages
131 - 154
Database
ISI
SICI code
0165-0378(200003)46:2<131:GCF(TM>2.0.ZU;2-U
Abstract
Factors in seminal plasma elicit a surge of GM-CSF expression in uterine ep ithelial cells after mating in mice. This study investigates the nature of the endometrial cell populations targeted by epithelial GM-CSF. In quantita tive RT-PCR studies, expression of the alpha-subunit of the GM-CSF receptor (GM-CSF-R) parallelled GM-CSF expression, being maximal during the 48 h pe riod after mating and declining thereafter. Expression of mRNA encoding bet a-common chain (AIC2B) also increased after mating and remained high until the time of embryo implantation on day 4 of pregnancy. Cells expressing GM- CSF receptors were identified in sections of uterus on the day after mating using I-125-GM-CSF, and were located predominantly in the endometrial stro ma subjacent to the luminal epithelium, co-localising with abundant populat ions of myeloid leukocytes. Cells expressing GM-CSF receptor were identifie d as macrophages, granulocytes and putative dendritic cells by flow cytomet ric analysis using lineage and receptor subunit specific antibodies. Recomb inant GM-CSF injected into the uterine lumen of ovariectomised mice was fou nd to elicit a dose-dependant accumulation of macrophages and granulocytes in the endometrium, in a pattern of distribution comparable to that seen in uteri after natural mating. Together, these data indicate a role for epith elial cell-derived GM-CSF in mediating the recruitment and potentially in m odifying the behaviour of uterine leukocytes during the post-mating inflamm atory response in mice. (C) 2000 Elsevier Science Ireland Ltd. All rights r eserved.