Sialyl Lewis X mediates interleukin-1 beta-induced trophoblast adhesion to endometrial cells during human embryo implantation.


Journal

Biology of reproduction
ISSN: 1529-7268
Titre abrégé: Biol Reprod
Pays: United States
ID NLM: 0207224

Informations de publication

Date de publication:
11 04 2023
Historique:
received: 14 07 2022
revised: 07 11 2022
accepted: 11 01 2023
medline: 18 4 2023
pubmed: 18 1 2023
entrez: 17 1 2023
Statut: ppublish

Résumé

Cell surface carbohydrate antigens sialyl Lewis X (sLeX) and Lewis Y (LeY) are paramount glycoconjugates and are abundantly expressed in the receptive endometrium. Furthermore, among the important biological functions of both antigens is their role in leukocytes adhesion and extravasation. Interleukin-1 beta (IL-1β) is involved in the process of human embryo implantation and placenta development. Here, we used an in vitro model to investigate whether sLeX and LeY are playing a role in the embryo implantation process mediated by IL-1β. Our results are showing that the expression of cell surface sLeX was enhanced in endometrial RL95-2 cells after exposure to IL-1β. RT-qPCR detection indicated that the transcript level of glycosyltransferase gene fucosyltransferase 3 (FUT3) was significantly elevated and that of FUT4/7 and ST3 beta-galactoside alpha-2,3-sialyltransferase 3/4 (ST3GAL3/4) were decreased by treatment with IL-1β. Modulatory role of glycosyltransferase FUT3 on sLeX biosynthesis was determined by FUT3 siRNA transfection in RL95-2 cells. Results showed that the expression level of sLeX was suppressed, but no change was observed in regard to LeY. Moreover, IL-1β promoted the HTR-8/SVneo trophoblast spheroids attachment to the RL95-2 endometrial monolayer, which was partially blocked by anti-sLeX antibody and FUT3 knockdown. Gene expression analysis of the RNA-seq transcriptome data from human secretory endometrium demonstrated a significantly higher level of FUT3 in the mid-secretory phase compared to the early secretory phase, which was correlated with the expression of IL1B. In summary, the inflammatory microenvironment at the fetomaternal interface can regulate the glycosylation pattern of endometrial cells at the time of implantation. SLeX can be significantly induced by IL-1β via increasing FUT3 expression, which facilitates the trophoblast adhesion during embryo implantation.

Identifiants

pubmed: 36648484
pii: 6989701
doi: 10.1093/biolre/ioad007
doi:

Substances chimiques

Fucosyltransferases EC 2.4.1.-
FUT4 protein, human EC 2.4.1.-
Glycosyltransferases EC 2.4.-
Interleukin-1beta 0
Sialyl Lewis X Antigen 0

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

564-574

Informations de copyright

© The Author(s) 2023. Published by Oxford University Press on behalf of Society for the Study of Reproduction. All rights reserved. For permissions, please e-mail: journals.permissions@oup.com.

Auteurs

Zhi Ma (Z)

Department of Obstetrics and Gynecology, University Hospital, Ludwig-Maximilians-Universität Munich, Munich, Germany.

Mirjana Kessler (M)

Department of Obstetrics and Gynecology, University Hospital, Ludwig-Maximilians-Universität Munich, Munich, Germany.

Anca Chelariu-Raicu (A)

Department of Obstetrics and Gynecology, University Hospital, Ludwig-Maximilians-Universität Munich, Munich, Germany.

Markus Sperandio (M)

Biomedical Center (BMC), Institute for Cardiovascular Physiology and Pathophysiology, Walter Brendel Center for Experimental Medicine (WBex), Faculty of Medicine, Ludwig-Maximilians-Universität Munich, Munich, Germany.

Sven Mahner (S)

Department of Obstetrics and Gynecology, University Hospital, Ludwig-Maximilians-Universität Munich, Munich, Germany.

Udo Jeschke (U)

Department of Obstetrics and Gynecology, University Hospital, Ludwig-Maximilians-Universität Munich, Munich, Germany.
Department of Obstetrics and Gynecology, University Hospital Augsburg, Augsburg, Germany.

Viktoria von Schönfeldt (V)

Department of Obstetrics and Gynecology, University Hospital, Ludwig-Maximilians-Universität Munich, Munich, Germany.

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Classifications MeSH