PMID- 23445935 OWN - NLM STAT- MEDLINE DCOM- 20130813 LR - 20211021 IS - 1471-2393 (Electronic) IS - 1471-2393 (Linking) VI - 13 Suppl 1 IP - Suppl 1 DP - 2013 TI - Maternal circulating leukocytes display early chemotactic responsiveness during late gestation. PG - S8 LID - 10.1186/1471-2393-13-S1-S8 [doi] AB - BACKGROUND: Parturition has been widely described as an immunological response; however, it is unknown how this is triggered. We hypothesized that an early event in parturition is an increased responsiveness of peripheral leukocytes to chemotactic stimuli expressed by reproductive tissues, and this precedes expression of tissue chemotactic activity, uterine activation and the systemic progesterone/estradiol shift. METHODS: Tissues and blood were collected from pregnant Long-Evans rats on gestational days (GD) 17, 20 and 22 (term gestation). We employed a validated Boyden chamber assay, flow cytometry, quantitative real time-polymerase chain reaction, and enzyme-linked immunosorbent assays. RESULTS: We found that GD20 maternal peripheral leukocytes migrated more than those from GD17 when these were tested with GD22 uterus and cervix extracts. Leukocytes on GD20 also displayed a significant increase in chemokine (C-C motif) ligand 2 (Ccl2) gene expression and this correlated with an increase in peripheral granulocyte proportions and a decrease in B cell and monocyte proportions. Tissue chemotactic activity and specific chemokines (CCL2, chemokine (C-X-C motif) ligand 1/CXCL1, and CXCL10) were mostly unchanged from GD17 to GD20 and increased only on GD22. CXCL10 peaked on GD20 in cervical tissues. As expected, prostaglandin F2alpha receptor and oxytocin receptor gene expression increased dramatically between GD20 and 22. Progesterone concentrations fell and estradiol-17beta concentrations increased in peripheral serum, cervical and uterine tissue extracts between GD20 and 22. CONCLUSION: Maternal circulating leukocytes display early chemotactic responsiveness, which leads to their infiltration into the uterus where they may participate in the process of parturition. FAU - Gomez-Lopez, Nardhy AU - Gomez-Lopez N AD - Department of Obstetrics and Gynecology, Pediatrics and Physiology, University of Alberta, Edmonton T6G 2S2, Canada. FAU - Tanaka, Satomi AU - Tanaka S FAU - Zaeem, Zoya AU - Zaeem Z FAU - Metz, Gerlinde A AU - Metz GA FAU - Olson, David M AU - Olson DM LA - eng PT - Journal Article PT - Research Support, Non-U.S. Gov't DEP - 20130131 PL - England TA - BMC Pregnancy Childbirth JT - BMC pregnancy and childbirth JID - 100967799 RN - 0 (Chemokines) RN - 0 (Receptors, Oxytocin) RN - 0 (Receptors, Prostaglandin) RN - 4G7DS2Q64Y (Progesterone) RN - 4TI98Z838E (Estradiol) SB - IM MH - Animals MH - Cervix Uteri/cytology/*metabolism MH - Chemokines/analysis/genetics/*metabolism MH - Chemotaxis, Leukocyte/immunology/*physiology MH - Enzyme-Linked Immunosorbent Assay MH - Estradiol/analysis MH - Female MH - Gene Expression MH - Leukocytes/*metabolism MH - Parturition/blood/immunology/*metabolism MH - Pregnancy MH - Pregnancy, Animal/*blood/immunology/metabolism MH - Progesterone/analysis MH - Rats MH - Rats, Long-Evans MH - Receptors, Oxytocin/blood/genetics MH - Receptors, Prostaglandin/blood/genetics PMC - PMC3561147 EDAT- 2013/03/06 06:00 MHDA- 2013/08/14 06:00 PMCR- 2013/01/31 CRDT- 2013/03/01 06:00 PHST- 2013/03/01 06:00 [entrez] PHST- 2013/03/06 06:00 [pubmed] PHST- 2013/08/14 06:00 [medline] PHST- 2013/01/31 00:00 [pmc-release] AID - 1471-2393-13-S1-S8 [pii] AID - 10.1186/1471-2393-13-S1-S8 [doi] PST - ppublish SO - BMC Pregnancy Childbirth. 2013;13 Suppl 1(Suppl 1):S8. doi: 10.1186/1471-2393-13-S1-S8. Epub 2013 Jan 31.