MicroRNAs emerging coordinate with placental mammals alter pathways in endometrial epithelia important for endometrial function

Summary: We tested the hypothesis that conserved placental mammal-specific microRNAs and their targets facilitate endometrial receptivity to implantation. Expression of miR-340-5p, -542-3p, and -671-5p was regulated by exposure of endometrial epithelial cells to progesterone (10 μg/ml) for 24 h coor...

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Main Authors: Laura Hume, Jessica C. Edge, Haidee Tinning, Dapeng T. Wang, Alysha S. Taylor, Vladimir Ovchinnikov, Annika V. Geijer-Simpson, Pavle Vrljicak, Jan J. Brosens, Emma S. Lucas, Nigel A.B. Simpson, Jayne Shillito, Karen Forbes, Mary J. O’Connell, Niamh Forde
Format: Article
Language:English
Published: Elsevier 2023-04-01
Series:iScience
Subjects:
Online Access:http://www.sciencedirect.com/science/article/pii/S2589004223004169
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author Laura Hume
Jessica C. Edge
Haidee Tinning
Dapeng T. Wang
Alysha S. Taylor
Vladimir Ovchinnikov
Annika V. Geijer-Simpson
Pavle Vrljicak
Jan J. Brosens
Emma S. Lucas
Nigel A.B. Simpson
Jayne Shillito
Karen Forbes
Mary J. O’Connell
Niamh Forde
author_facet Laura Hume
Jessica C. Edge
Haidee Tinning
Dapeng T. Wang
Alysha S. Taylor
Vladimir Ovchinnikov
Annika V. Geijer-Simpson
Pavle Vrljicak
Jan J. Brosens
Emma S. Lucas
Nigel A.B. Simpson
Jayne Shillito
Karen Forbes
Mary J. O’Connell
Niamh Forde
author_sort Laura Hume
collection DOAJ
description Summary: We tested the hypothesis that conserved placental mammal-specific microRNAs and their targets facilitate endometrial receptivity to implantation. Expression of miR-340-5p, -542-3p, and -671-5p was regulated by exposure of endometrial epithelial cells to progesterone (10 μg/ml) for 24 h coordinate with 1,713 of their predicted targets. Proteomic analysis of cells transfected with miRNA mimic/inhibitor (48 h: n = 3) revealed 1,745 proteins altered by miR-340-5p (mimic; 1,369, inhibitor; 376) of which 171 were predicted targets and P4-regulated. MiR-542-3p altered 2,353 (mimic; 1,378, inhibitor; 975) 100 which were mirDB predicted, including 46 P4-regulated. MiR-671-5p altered 1,744 proteins (mimic; 1,252, inhibitor; 492) 95 of which were predicted targets and 46 P4-regulated. All miRNAs were detected in luteal phase endometrial biopsies, irrespective of pregnancy outcomes. miR-340-5p expression increased in biopsies from individuals suffering previous and subsequent miscarriage compared to those with subsequent live birth. Dysfunction of these miRNAs and their targets contribute to endometrial-derived recurrent pregnancy loss.
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spelling doaj.art-53288b4ef1ff4e27859d5eecc43cebec2023-03-19T04:38:21ZengElsevieriScience2589-00422023-04-01264106339MicroRNAs emerging coordinate with placental mammals alter pathways in endometrial epithelia important for endometrial functionLaura Hume0Jessica C. Edge1Haidee Tinning2Dapeng T. Wang3Alysha S. Taylor4Vladimir Ovchinnikov5Annika V. Geijer-Simpson6Pavle Vrljicak7Jan J. Brosens8Emma S. Lucas9Nigel A.B. Simpson10Jayne Shillito11Karen Forbes12Mary J. O’Connell13Niamh Forde14Discovery and Translational Sciences Department, Leeds Institute of Cardiovascular and Metabolic Medicine, Faculty of Medicine and Health, University of Leeds, Leeds, LS2 9JT, UKDiscovery and Translational Sciences Department, Leeds Institute of Cardiovascular and Metabolic Medicine, Faculty of Medicine and Health, University of Leeds, Leeds, LS2 9JT, UKDiscovery and Translational Sciences Department, Leeds Institute of Cardiovascular and Metabolic Medicine, Faculty of Medicine and Health, University of Leeds, Leeds, LS2 9JT, UKLeedsOmics, University of Leeds, Leeds, UKDiscovery and Translational Sciences Department, Leeds Institute of Cardiovascular and Metabolic Medicine, Faculty of Medicine and Health, University of Leeds, Leeds, LS2 9JT, UK; School of Biology, Faculty of Biological Sciences, University of Leeds, Leeds, LS2 9JT, UKSchool of Life Sciences, Faculty of Medicine and Health Sciences, University of Nottingham, Nottingham, NG7 2RD, UKDiscovery and Translational Sciences Department, Leeds Institute of Cardiovascular and Metabolic Medicine, Faculty of Medicine and Health, University of Leeds, Leeds, LS2 9JT, UK; School of Biology, Faculty of Biological Sciences, University of Leeds, Leeds, LS2 9JT, UKDivision of Biomedical Sciences, Clinical Sciences Research Laboratories, Warwick Medical School, University of Warwick, Coventry CV2 2DX, UKDivision of Biomedical Sciences, Clinical Sciences Research Laboratories, Warwick Medical School, University of Warwick, Coventry CV2 2DX, UK; Tommy’s National Centre for Miscarriage Research, University Hospital Coventry and Warwickshire, Coventry CV2 2DX, UKDivision of Biomedical Sciences, Clinical Sciences Research Laboratories, Warwick Medical School, University of Warwick, Coventry CV2 2DX, UKDepartment of Women’s and Children’s Health, School of Medicine, University of Leeds, Leeds LS2 9JT, UK; Leeds Teaching Hospitals Trust, Beckett St, Leeds LS9 7TF, UKLeeds Teaching Hospitals Trust, Beckett St, Leeds LS9 7TF, UKDiscovery and Translational Sciences Department, Leeds Institute of Cardiovascular and Metabolic Medicine, Faculty of Medicine and Health, University of Leeds, Leeds, LS2 9JT, UKSchool of Life Sciences, Faculty of Medicine and Health Sciences, University of Nottingham, Nottingham, NG7 2RD, UKDiscovery and Translational Sciences Department, Leeds Institute of Cardiovascular and Metabolic Medicine, Faculty of Medicine and Health, University of Leeds, Leeds, LS2 9JT, UK; Corresponding authorSummary: We tested the hypothesis that conserved placental mammal-specific microRNAs and their targets facilitate endometrial receptivity to implantation. Expression of miR-340-5p, -542-3p, and -671-5p was regulated by exposure of endometrial epithelial cells to progesterone (10 μg/ml) for 24 h coordinate with 1,713 of their predicted targets. Proteomic analysis of cells transfected with miRNA mimic/inhibitor (48 h: n = 3) revealed 1,745 proteins altered by miR-340-5p (mimic; 1,369, inhibitor; 376) of which 171 were predicted targets and P4-regulated. MiR-542-3p altered 2,353 (mimic; 1,378, inhibitor; 975) 100 which were mirDB predicted, including 46 P4-regulated. MiR-671-5p altered 1,744 proteins (mimic; 1,252, inhibitor; 492) 95 of which were predicted targets and 46 P4-regulated. All miRNAs were detected in luteal phase endometrial biopsies, irrespective of pregnancy outcomes. miR-340-5p expression increased in biopsies from individuals suffering previous and subsequent miscarriage compared to those with subsequent live birth. Dysfunction of these miRNAs and their targets contribute to endometrial-derived recurrent pregnancy loss.http://www.sciencedirect.com/science/article/pii/S2589004223004169Biological sciencesMolecular biologyDevelopmental biologyEmbryology
spellingShingle Laura Hume
Jessica C. Edge
Haidee Tinning
Dapeng T. Wang
Alysha S. Taylor
Vladimir Ovchinnikov
Annika V. Geijer-Simpson
Pavle Vrljicak
Jan J. Brosens
Emma S. Lucas
Nigel A.B. Simpson
Jayne Shillito
Karen Forbes
Mary J. O’Connell
Niamh Forde
MicroRNAs emerging coordinate with placental mammals alter pathways in endometrial epithelia important for endometrial function
iScience
Biological sciences
Molecular biology
Developmental biology
Embryology
title MicroRNAs emerging coordinate with placental mammals alter pathways in endometrial epithelia important for endometrial function
title_full MicroRNAs emerging coordinate with placental mammals alter pathways in endometrial epithelia important for endometrial function
title_fullStr MicroRNAs emerging coordinate with placental mammals alter pathways in endometrial epithelia important for endometrial function
title_full_unstemmed MicroRNAs emerging coordinate with placental mammals alter pathways in endometrial epithelia important for endometrial function
title_short MicroRNAs emerging coordinate with placental mammals alter pathways in endometrial epithelia important for endometrial function
title_sort micrornas emerging coordinate with placental mammals alter pathways in endometrial epithelia important for endometrial function
topic Biological sciences
Molecular biology
Developmental biology
Embryology
url http://www.sciencedirect.com/science/article/pii/S2589004223004169
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