Fractalkine Regulates HEC-1A/JEG-3 Interaction by Influencing the Expression of Implantation-Related Genes in an In Vitro Co-Culture Model

Embryo implantation is a complex process regulated by a network of biological molecules. Recently, it has been described that fractalkine (CX3CL1, FKN) might have an important role in the feto–maternal interaction during gestation since the trophoblast cells express fractalkine receptor (CX3CR1) and...

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Main Authors: Ramóna Pap, Gergely Montskó, Gergely Jánosa, Katalin Sipos, Gábor L. Kovács, Edina Pandur
Format: Article
Language:English
Published: MDPI AG 2020-04-01
Series:International Journal of Molecular Sciences
Subjects:
Online Access:https://www.mdpi.com/1422-0067/21/9/3175
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author Ramóna Pap
Gergely Montskó
Gergely Jánosa
Katalin Sipos
Gábor L. Kovács
Edina Pandur
author_facet Ramóna Pap
Gergely Montskó
Gergely Jánosa
Katalin Sipos
Gábor L. Kovács
Edina Pandur
author_sort Ramóna Pap
collection DOAJ
description Embryo implantation is a complex process regulated by a network of biological molecules. Recently, it has been described that fractalkine (CX3CL1, FKN) might have an important role in the feto–maternal interaction during gestation since the trophoblast cells express fractalkine receptor (CX3CR1) and the endometrium cells secrete fractalkine. CX3CR1 controls three major signalling pathways, PLC-PKC pathway, PI3K/AKT/NFκB pathway and Ras-mitogen-activated protein kinases (MAPK) pathways regulating proliferation, growth, migration and apoptosis. In this study, we focused on the molecular mechanisms of FKN treatment influencing the expression of implantation-related genes in trophoblast cells (JEG-3) both in mono-and in co-culture models. Our results reveal that FKN acted in a concentration and time dependent manner on JEG-3 cells. FKN seemed to operate as a positive regulator of implantation via changing the action of progesterone receptor (PR), activin receptor and bone morphogenetic protein receptor (BMPR). FKN modified also the expression of matrix metalloproteinase 2 and 9 controlling invasion. The presence of HEC-1A endometrial cells in the co-culture contributed to the effect of fractalkine on JEG-3 cells regulating implantation. The results suggest that FKN may contribute to the successful attachment and implantation of embryo.
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spelling doaj.art-2485e6f8be6d4da494617b7ce828e5212023-11-19T23:08:38ZengMDPI AGInternational Journal of Molecular Sciences1661-65961422-00672020-04-01219317510.3390/ijms21093175Fractalkine Regulates HEC-1A/JEG-3 Interaction by Influencing the Expression of Implantation-Related Genes in an In Vitro Co-Culture ModelRamóna Pap0Gergely Montskó1Gergely Jánosa2Katalin Sipos3Gábor L. Kovács4Edina Pandur5Department of Pharmaceutical Biology, Faculty of Pharmacy, University of Pécs, H-7624 Pécs, HungarySzentágothai Research Centre, University of Pécs, H-7624 Pécs, HungaryDepartment of Pharmaceutical Biology, Faculty of Pharmacy, University of Pécs, H-7624 Pécs, HungaryDepartment of Pharmaceutical Biology, Faculty of Pharmacy, University of Pécs, H-7624 Pécs, HungarySzentágothai Research Centre, University of Pécs, H-7624 Pécs, HungaryDepartment of Pharmaceutical Biology, Faculty of Pharmacy, University of Pécs, H-7624 Pécs, HungaryEmbryo implantation is a complex process regulated by a network of biological molecules. Recently, it has been described that fractalkine (CX3CL1, FKN) might have an important role in the feto–maternal interaction during gestation since the trophoblast cells express fractalkine receptor (CX3CR1) and the endometrium cells secrete fractalkine. CX3CR1 controls three major signalling pathways, PLC-PKC pathway, PI3K/AKT/NFκB pathway and Ras-mitogen-activated protein kinases (MAPK) pathways regulating proliferation, growth, migration and apoptosis. In this study, we focused on the molecular mechanisms of FKN treatment influencing the expression of implantation-related genes in trophoblast cells (JEG-3) both in mono-and in co-culture models. Our results reveal that FKN acted in a concentration and time dependent manner on JEG-3 cells. FKN seemed to operate as a positive regulator of implantation via changing the action of progesterone receptor (PR), activin receptor and bone morphogenetic protein receptor (BMPR). FKN modified also the expression of matrix metalloproteinase 2 and 9 controlling invasion. The presence of HEC-1A endometrial cells in the co-culture contributed to the effect of fractalkine on JEG-3 cells regulating implantation. The results suggest that FKN may contribute to the successful attachment and implantation of embryo.https://www.mdpi.com/1422-0067/21/9/3175fractalkineimplantationendometriumtrophoblastbilaminar co-culture
spellingShingle Ramóna Pap
Gergely Montskó
Gergely Jánosa
Katalin Sipos
Gábor L. Kovács
Edina Pandur
Fractalkine Regulates HEC-1A/JEG-3 Interaction by Influencing the Expression of Implantation-Related Genes in an In Vitro Co-Culture Model
International Journal of Molecular Sciences
fractalkine
implantation
endometrium
trophoblast
bilaminar co-culture
title Fractalkine Regulates HEC-1A/JEG-3 Interaction by Influencing the Expression of Implantation-Related Genes in an In Vitro Co-Culture Model
title_full Fractalkine Regulates HEC-1A/JEG-3 Interaction by Influencing the Expression of Implantation-Related Genes in an In Vitro Co-Culture Model
title_fullStr Fractalkine Regulates HEC-1A/JEG-3 Interaction by Influencing the Expression of Implantation-Related Genes in an In Vitro Co-Culture Model
title_full_unstemmed Fractalkine Regulates HEC-1A/JEG-3 Interaction by Influencing the Expression of Implantation-Related Genes in an In Vitro Co-Culture Model
title_short Fractalkine Regulates HEC-1A/JEG-3 Interaction by Influencing the Expression of Implantation-Related Genes in an In Vitro Co-Culture Model
title_sort fractalkine regulates hec 1a jeg 3 interaction by influencing the expression of implantation related genes in an in vitro co culture model
topic fractalkine
implantation
endometrium
trophoblast
bilaminar co-culture
url https://www.mdpi.com/1422-0067/21/9/3175
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