[HTML][HTML] The chemokine receptor CXCR4 and its ligand CXCL12 are activated during implantation and placentation in sheep
Reproductive Biology and Endocrinology, 2011•Springer
Background The progression of implantation and placentation in ruminants is complex and
is regulated by interplay between sex steroids and local signaling molecules, many of which
have immune function. Chemokines and their receptors are pivotal factors in implantation
and vascularization of the placenta. Based on known critical roles for chemokine receptor 4
(CXCR4) during early pregnancy in other species, we hypothesized that CXCR4 and its
ligand CXCL12 would increase in the endometrium and conceptus in response to …
is regulated by interplay between sex steroids and local signaling molecules, many of which
have immune function. Chemokines and their receptors are pivotal factors in implantation
and vascularization of the placenta. Based on known critical roles for chemokine receptor 4
(CXCR4) during early pregnancy in other species, we hypothesized that CXCR4 and its
ligand CXCL12 would increase in the endometrium and conceptus in response to …
Background
The progression of implantation and placentation in ruminants is complex and is regulated by interplay between sex steroids and local signaling molecules, many of which have immune function. Chemokines and their receptors are pivotal factors in implantation and vascularization of the placenta. Based on known critical roles for chemokine receptor 4 (CXCR4) during early pregnancy in other species, we hypothesized that CXCR4 and its ligand CXCL12 would increase in the endometrium and conceptus in response to implantation in ewes. The objectives of the current study were to determine if CXCL12 and CXCR4 were upregulated in: endometrium from pregnant compared to non-pregnant ewes and in, conceptuses, cotyledons, caruncles and intercaruncular tissue.
Methods
Tissues were collected from sheep on Days 12, 13, 14, and 15 of either the estrous cycle or pregnancy and from pregnant ewes on Days 35 and 50. Blood samples from jugular and uterine vein were also collected on all days. Conceptuses were collected from mature ewes on Days 13, 15, 16, 17, 21 and 30 of gestation. Real time PCR was used to determine relative mRNA concentrations for CXCL12 and CXCR4 and Western blot analysis was employed to confirm protein concentration.
Results
Differences described are P < 0.05. In the endometrium, CXCR4 mRNA and protein was greater on Day 15 of pregnancy compared to the estrous cycle. CXCL12 and CXCR4 mRNA in conceptuses was greater on Days 21 and 30 compared to earlier days. CXCL12 mRNA was greater in cotyledons on Day 35 compared to Day 50. On Day 35 of gestation, CXCR4 was greater compared to Day 50 in caruncle and intercaruncular tissue. White blood cells obtained from jugular and uterine vein collection had the greatest mRNA concentration of CXCL12 on Day 35 of pregnancy.
Conclusions
A comprehensive analysis of CXCL12 and CXCR4 expression in fetal and maternal tissues during early pregnancy is reported with noteworthy differences occurring during implantation and placentation in sheep. We interpreted these data to mean that the CXCL12/CXCR4 pathway is activated during implantation and placentation in sheep and is likely playing a role in the communication between trophoblast cells and the maternal endometrium.
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