NK cell-derived IL-10 is critical for DC-NK cell dialogue at the maternal-fetal interface

Abstract DC-NK cell interactions are thought to influence the development of maternal tolerance and de novo angiogenesis during early gestation. However, it is unclear which mechanism ensures the cooperative dialogue between DC and NK cells at the feto-maternal interface. In this article, we show th...

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Autores principales: Sandra M. Blois, Nancy Freitag, Irene Tirado-González, Shi-Bin Cheng, Markus M. Heimesaat, Stefan Bereswill, Matthias Rose, Melanie L. Conrad, Gabriela Barrientos, Surendra Sharma
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Publicado: Nature Portfolio 2017
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Acceso en línea:https://doaj.org/article/4ec6071fecc54e49b9946a5938c4c326
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spelling oai:doaj.org-article:4ec6071fecc54e49b9946a5938c4c3262021-12-02T15:05:48ZNK cell-derived IL-10 is critical for DC-NK cell dialogue at the maternal-fetal interface10.1038/s41598-017-02333-82045-2322https://doaj.org/article/4ec6071fecc54e49b9946a5938c4c3262017-05-01T00:00:00Zhttps://doi.org/10.1038/s41598-017-02333-8https://doaj.org/toc/2045-2322Abstract DC-NK cell interactions are thought to influence the development of maternal tolerance and de novo angiogenesis during early gestation. However, it is unclear which mechanism ensures the cooperative dialogue between DC and NK cells at the feto-maternal interface. In this article, we show that uterine NK cells are the key source of IL-10 that is required to regulate DC phenotype and pregnancy success. Upon in vivo expansion of DC during early gestation, NK cells expressed increased levels of IL-10. Exogenous administration of IL-10 was sufficient to overcome early pregnancy failure in dams treated to achieve simultaneous DC expansion and NK cell depletion. Remarkably, DC expansion in IL-10−/− dams provoked pregnancy loss, which could be abrogated by the adoptive transfer of IL-10+/+ NK cells and not by IL-10−/− NK cells. Furthermore, the IL-10 expressing NK cells markedly enhanced angiogenic responses and placental development in DC expanded IL-10−/− dams. Thus, the capacity of NK cells to secrete IL-10 plays a unique role facilitating the DC-NK cell dialogue during the establishment of a healthy gestation.Sandra M. BloisNancy FreitagIrene Tirado-GonzálezShi-Bin ChengMarkus M. HeimesaatStefan BereswillMatthias RoseMelanie L. ConradGabriela BarrientosSurendra SharmaNature PortfolioarticleMedicineRScienceQENScientific Reports, Vol 7, Iss 1, Pp 1-9 (2017)
institution DOAJ
collection DOAJ
language EN
topic Medicine
R
Science
Q
spellingShingle Medicine
R
Science
Q
Sandra M. Blois
Nancy Freitag
Irene Tirado-González
Shi-Bin Cheng
Markus M. Heimesaat
Stefan Bereswill
Matthias Rose
Melanie L. Conrad
Gabriela Barrientos
Surendra Sharma
NK cell-derived IL-10 is critical for DC-NK cell dialogue at the maternal-fetal interface
description Abstract DC-NK cell interactions are thought to influence the development of maternal tolerance and de novo angiogenesis during early gestation. However, it is unclear which mechanism ensures the cooperative dialogue between DC and NK cells at the feto-maternal interface. In this article, we show that uterine NK cells are the key source of IL-10 that is required to regulate DC phenotype and pregnancy success. Upon in vivo expansion of DC during early gestation, NK cells expressed increased levels of IL-10. Exogenous administration of IL-10 was sufficient to overcome early pregnancy failure in dams treated to achieve simultaneous DC expansion and NK cell depletion. Remarkably, DC expansion in IL-10−/− dams provoked pregnancy loss, which could be abrogated by the adoptive transfer of IL-10+/+ NK cells and not by IL-10−/− NK cells. Furthermore, the IL-10 expressing NK cells markedly enhanced angiogenic responses and placental development in DC expanded IL-10−/− dams. Thus, the capacity of NK cells to secrete IL-10 plays a unique role facilitating the DC-NK cell dialogue during the establishment of a healthy gestation.
format article
author Sandra M. Blois
Nancy Freitag
Irene Tirado-González
Shi-Bin Cheng
Markus M. Heimesaat
Stefan Bereswill
Matthias Rose
Melanie L. Conrad
Gabriela Barrientos
Surendra Sharma
author_facet Sandra M. Blois
Nancy Freitag
Irene Tirado-González
Shi-Bin Cheng
Markus M. Heimesaat
Stefan Bereswill
Matthias Rose
Melanie L. Conrad
Gabriela Barrientos
Surendra Sharma
author_sort Sandra M. Blois
title NK cell-derived IL-10 is critical for DC-NK cell dialogue at the maternal-fetal interface
title_short NK cell-derived IL-10 is critical for DC-NK cell dialogue at the maternal-fetal interface
title_full NK cell-derived IL-10 is critical for DC-NK cell dialogue at the maternal-fetal interface
title_fullStr NK cell-derived IL-10 is critical for DC-NK cell dialogue at the maternal-fetal interface
title_full_unstemmed NK cell-derived IL-10 is critical for DC-NK cell dialogue at the maternal-fetal interface
title_sort nk cell-derived il-10 is critical for dc-nk cell dialogue at the maternal-fetal interface
publisher Nature Portfolio
publishDate 2017
url https://doaj.org/article/4ec6071fecc54e49b9946a5938c4c326
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