Oxygen regulates ILC3 antigen presentation potential and pregnancy-related hormone actions

Abstract Early pregnancy is marked by placentation and embryogenesis, which take place under physiological low oxygen concentrations. This oxygen condition is crucial for many aspects of placentation, trophoblast function, vascularization and immune function. Recently, a new family of innate lymphoi...

Full description

Bibliographic Details
Main Authors: Rebekka Einenkel, Jens Ehrhardt, Marek Zygmunt, Damián Oscar Muzzio
Format: Article
Language:English
Published: BMC 2022-07-01
Series:Reproductive Biology and Endocrinology
Subjects:
Online Access:https://doi.org/10.1186/s12958-022-00979-2
_version_ 1828375162372751360
author Rebekka Einenkel
Jens Ehrhardt
Marek Zygmunt
Damián Oscar Muzzio
author_facet Rebekka Einenkel
Jens Ehrhardt
Marek Zygmunt
Damián Oscar Muzzio
author_sort Rebekka Einenkel
collection DOAJ
description Abstract Early pregnancy is marked by placentation and embryogenesis, which take place under physiological low oxygen concentrations. This oxygen condition is crucial for many aspects of placentation, trophoblast function, vascularization and immune function. Recently, a new family of innate lymphoid cells has been found to be expressed at the fetomaternal interface. Among these, type 3 innate lymphoid cells (ILC3) are important antigen presenting cells in the context of MHC-II. The expression of MHC-II on ILC3s during pregnancy is reduced. We tested the hypothesis that low oxygen concentrations reduce the potential of ILC3s to present antigens promoting fetal tolerance. Using an in vitro approach, NCR+ ILC3s generated from cord blood stem cell precursors were incubated under different O2 concentrations in the presence or absence of the pregnancy-related hormones hCG and TGF-β1. The expression of MHC-II, accessory molecules and an activation marker were assessed by flow cytometry. We observed that 1% O2 reduced the expression of the MHC-II molecule HLA-DR as compared to 21% O2 and modulated the relative effects of hCG and TGF-β1. Our data indicate that low oxygen concentrations reduce the antigen presentation potential of NCR+ ILC3s and suggest that it may promote fetal tolerance during the first trimester of pregnancy.
first_indexed 2024-04-14T07:43:53Z
format Article
id doaj.art-fed720e7aae14c29976414f943c14823
institution Directory Open Access Journal
issn 1477-7827
language English
last_indexed 2024-04-14T07:43:53Z
publishDate 2022-07-01
publisher BMC
record_format Article
series Reproductive Biology and Endocrinology
spelling doaj.art-fed720e7aae14c29976414f943c148232022-12-22T02:05:25ZengBMCReproductive Biology and Endocrinology1477-78272022-07-012011910.1186/s12958-022-00979-2Oxygen regulates ILC3 antigen presentation potential and pregnancy-related hormone actionsRebekka Einenkel0Jens Ehrhardt1Marek Zygmunt2Damián Oscar Muzzio3Department of Obstetrics and Gynecology, University Medicine GreifswaldDepartment of Obstetrics and Gynecology, University Medicine GreifswaldDepartment of Obstetrics and Gynecology, University Medicine GreifswaldDepartment of Obstetrics and Gynecology, University Medicine GreifswaldAbstract Early pregnancy is marked by placentation and embryogenesis, which take place under physiological low oxygen concentrations. This oxygen condition is crucial for many aspects of placentation, trophoblast function, vascularization and immune function. Recently, a new family of innate lymphoid cells has been found to be expressed at the fetomaternal interface. Among these, type 3 innate lymphoid cells (ILC3) are important antigen presenting cells in the context of MHC-II. The expression of MHC-II on ILC3s during pregnancy is reduced. We tested the hypothesis that low oxygen concentrations reduce the potential of ILC3s to present antigens promoting fetal tolerance. Using an in vitro approach, NCR+ ILC3s generated from cord blood stem cell precursors were incubated under different O2 concentrations in the presence or absence of the pregnancy-related hormones hCG and TGF-β1. The expression of MHC-II, accessory molecules and an activation marker were assessed by flow cytometry. We observed that 1% O2 reduced the expression of the MHC-II molecule HLA-DR as compared to 21% O2 and modulated the relative effects of hCG and TGF-β1. Our data indicate that low oxygen concentrations reduce the antigen presentation potential of NCR+ ILC3s and suggest that it may promote fetal tolerance during the first trimester of pregnancy.https://doi.org/10.1186/s12958-022-00979-2Innate lymphoid cellsOxygenhCGTGF-β1PregnancyTolerance
spellingShingle Rebekka Einenkel
Jens Ehrhardt
Marek Zygmunt
Damián Oscar Muzzio
Oxygen regulates ILC3 antigen presentation potential and pregnancy-related hormone actions
Reproductive Biology and Endocrinology
Innate lymphoid cells
Oxygen
hCG
TGF-β1
Pregnancy
Tolerance
title Oxygen regulates ILC3 antigen presentation potential and pregnancy-related hormone actions
title_full Oxygen regulates ILC3 antigen presentation potential and pregnancy-related hormone actions
title_fullStr Oxygen regulates ILC3 antigen presentation potential and pregnancy-related hormone actions
title_full_unstemmed Oxygen regulates ILC3 antigen presentation potential and pregnancy-related hormone actions
title_short Oxygen regulates ILC3 antigen presentation potential and pregnancy-related hormone actions
title_sort oxygen regulates ilc3 antigen presentation potential and pregnancy related hormone actions
topic Innate lymphoid cells
Oxygen
hCG
TGF-β1
Pregnancy
Tolerance
url https://doi.org/10.1186/s12958-022-00979-2
work_keys_str_mv AT rebekkaeinenkel oxygenregulatesilc3antigenpresentationpotentialandpregnancyrelatedhormoneactions
AT jensehrhardt oxygenregulatesilc3antigenpresentationpotentialandpregnancyrelatedhormoneactions
AT marekzygmunt oxygenregulatesilc3antigenpresentationpotentialandpregnancyrelatedhormoneactions
AT damianoscarmuzzio oxygenregulatesilc3antigenpresentationpotentialandpregnancyrelatedhormoneactions