| Literature DB >> 29768178 |
Moriya Gamliel1, Debra Goldman-Wohl2, Batya Isaacson1, Chamutal Gur1, Natan Stein1, Rachel Yamin1, Michael Berger1, Myriam Grunewald3, Eli Keshet3, Yoach Rais4, Chamutal Bornstein5, Eyal David5, Adam Jelinski5, Iris Eisenberg2, Caryn Greenfield2, Arbel Ben-David2, Tal Imbar2, Ronit Gilad2, Ronit Haimov-Kochman2, David Mankuta6, Matan Elami-Suzin6, Ido Amit5, Jacob H Hanna4, Simcha Yagel2, Ofer Mandelboim7.
Abstract
Natural killer cells (NKs) are abundant in the human decidua, regulating trophoblast invasion and angiogenesis. Several diseases of poor placental development are associated with first pregnancies, so we thus looked to characterize differences in decidual NKs (dNKs) in first versus repeated pregnancies. We discovered a population found in repeated pregnancies, which has a unique transcriptome and epigenetic signature, and is characterized by high expression of the receptors NKG2C and LILRB1. We named these cells Pregnancy Trained decidual NK cells (PTdNKs). PTdNKs have open chromatin around the enhancers of IFNG and VEGFA. Activation of PTdNKs led to increased production and secretion of IFN-γ and VEGFα, with the latter supporting vascular sprouting and tumor growth. The precursors of PTdNKs seem to be found in the endometrium. Because repeated pregnancies are associated with improved placentation, we propose that PTdNKs, which are present primarily in repeated pregnancies, might be involved in proper placentation.Entities:
Keywords: LILRB1; NKG2C; decidua; gravidity; great obstetrical disorders; natural killer cells; pregnancy; trained immunity
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Year: 2018 PMID: 29768178 DOI: 10.1016/j.immuni.2018.03.030
Source DB: PubMed Journal: Immunity ISSN: 1074-7613 Impact factor: 31.745