0000000000476738

AUTHOR

Nuria Balaguer

showing 5 related works from this author

Heterogeneous nuclear ribonucleoprotein C1 may control miR-30d levels in endometrial exosomes affecting early embryo implantation.

2018

Study question Is there a specific mechanism to load the microRNA (miRNA), hsa-miR-30d, into exosomes to facilitate maternal communication with preimplantation embryos? Summary answer The heterogeneous nuclear ribonucleoprotein C1 (hnRNPC1) is involved in the internalization of endometrial miR-30d into exosomes to prepare for its subsequent incorporation into trophectoderm cells. What is known already Our group previously described a novel cell-to-cell communication mechanism involving the delivery of endometrial miRNAs from the maternal endometrium to the trophectoderm cells of preimplantation embryos. Specifically, human endometrial miR-30d is taken up by murine blastocysts causing the ov…

0301 basic medicineEmbryologyHeterogeneous nuclear ribonucleoproteinBiologyExosomesFlow cytometry03 medical and health sciencesEndometriumMiceTandem Mass SpectrometryGeneticsmedicineAnimalsHumansBlastocystEmbryo ImplantationMolecular Biologymedicine.diagnostic_testHeterogeneous-Nuclear Ribonucleoprotein Group CObstetrics and GynecologyEmbryoCell BiologyTransfectionMolecular biologyEmbryonic stem cellMicrovesiclesCoculture TechniquesBlotMicroRNAs030104 developmental biologymedicine.anatomical_structureReproductive MedicineFemaleDevelopmental BiologyMolecular human reproduction
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Hsa-miR-30d, secreted by the human endometrium, is taken up by the pre-implantation embryo and might modify its transcriptome.

2015

During embryo implantation, the blastocyst interacts with and regulates the endometrium, and endometrial fluid secreted by the endometrial epithelium nurtures the embryo. Here, we propose that maternal microRNAs (miRNAs) might act as transcriptomic modifier of the pre-implantation embryo. Microarray profiling revealed that six of 27 specific, maternal miRNAs were differentially expressed in the human endometrial epithelium during the window of implantation – a brief phase of endometrial receptivity to the blastocyst – and were released into the endometrial fluid. Further investigation revealed that hsa-miR-30d, the expression levels of which were most significantly upregulated, was secreted…

Endometrial fluidanimal structuresBlotting WesternEmbryonic DevelopmentBiologyEndometriumPolymerase Chain ReactionTranscriptomeEndometriumMiceMicroscopy Electron TransmissionmicroRNAmedicineAnimalsHumansBlastocystMolecular BiologyEmbryo adhesionPre-implantation embryoMicroarray analysis techniquesEmbryogenesisGene Expression Regulation DevelopmentalEmbryoMicroarray AnalysisMolecular biologyEmbryonic stem cellImmunohistochemistryCell biologyHas-miR-30dMicroRNAsmedicine.anatomical_structureBlastocystMicroscopy Fluorescenceembryonic structuresFemaleTranscriptomeDevelopmental BiologyDevelopment (Cambridge, England)
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MicroRNA-30d deficiency during preconception affects endometrial receptivity by decreasing implantation rates and impairing fetal growth.

2019

Background Maternal–embryonic crosstalk between the endometrium and the preimplantation embryo is required for normal pregnancy. Our previous results demonstrated that maternal microRNAs secreted into the endometrial fluid, specifically miR-30d, act as a transcriptomic regulator of the preimplantation embryo by the maternal intrauterine environment. Objective To investigate the reproductive and fetal effects of murine miR-30d deficiency at the maternal–embryonic interface according to the origin of its maternal or embryonic default. Study Design A miR-30d knockout murine model was used as the animal model to investigate the impact of maternal and/or embryonic origin of miR-30d deficiency on…

PlacentaEndometriumReal-Time Polymerase Chain ReactionLeukemia Inhibitory FactorAndrologyFetal Development03 medical and health sciencesEndometriumMice0302 clinical medicinePregnancymedicineAnimals030212 general & internal medicineEmbryo ImplantationHomeodomain ProteinsMSX1 Transcription FactorMice KnockoutFetusPregnancy030219 obstetrics & reproductive medicinebusiness.industryObstetrics and GynecologyGene Expression Regulation DevelopmentalEmbryomedicine.diseaseEmbryo TransferEmbryonic stem cellPlacentationMicroRNAsmedicine.anatomical_structureReal-time polymerase chain reactionReceptors EstrogenCyclooxygenase 2GestationSmall for gestational ageFemalebusinessReceptors ProgesteroneAmerican journal of obstetrics and gynecology
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Extracellular Vesicles in Human Reproduction in Health and Disease.

2017

Extensive evidence suggests that the release of membrane-enclosed compartments, more commonly known as extracellular vesicles (EVs), is a potent newly identified mechanism of cell-to-cell communication both in normal physiology and in pathological conditions. This review presents evidence about the formation and release of different EVs, their definitive markers and cargo content in reproductive physiological processes, and their capacity to convey information between cells through the transfer of functional protein and genetic information to alter phenotype and function of recipient cells associated with reproductive biology. In the male reproductive tract, epididymosomes and prostasomes p…

0301 basic medicineMaleCell signalingEndocrinology Diabetes and MetabolismAcrosome reactionCell CommunicationBiology03 medical and health sciencesHuman reproductionExtracellular Vesicles0302 clinical medicineEndocrinologyErectile DysfunctionCapacitationPregnancyReproductive biologyHumansEmbryo ImplantationSperm motilityReproductionCell biologyPregnancy Complications030104 developmental biology030220 oncology & carcinogenesisOocytesSperm MotilityOviductProstasomesFemaleGenital Diseases FemaleEndocrine reviews
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Should Vanishing Twin Pregnancies Be Systematically Excluded From Cell-Free Fetal DNA Testing?

2020

Objective To demonstrate the feasibility of cell-free DNA (cfDNA) testing in vanishing twin (VT) pregnancies in routine clinical practice. Methods Our study included 24 874 singleton and 206 VT consecutive pregnancies. Cell-free DNA was analyzed by massively parallel sequencing. Both aneuploidy analysis (chromosomes 13,18, 21, X, and Y) and fetal fraction estimation were performed according to an Illumina algorithm. Contaminant DNA contribution from the demised co-twin was studied in detail. Results VT pregnancies exhibited a higher prevalence of screen-positive cases (5.8% vs 2.5%), sex discrepancies (10.2% vs 0.05%), and false positive rates (FPR) (2.6% vs 0.3%) than singleton pregnancies…

Adult0301 basic medicinemedicine.medical_specialtyAneuploidy030105 genetics & heredity03 medical and health sciences0302 clinical medicinePregnancyPrenatal DiagnosisHumansMedicineGenetics (clinical)Retrospective StudiesVanishing twinFetusPregnancy030219 obstetrics & reproductive medicinebusiness.industryObstetricsSingletonIncidence (epidemiology)Obstetrics and GynecologyGeneral Medicinemedicine.diseaseCell-free fetal DNAPregnancy TwinFemalebusinessTrisomyCell-Free Nucleic AcidsObstetrical & Gynecological Survey
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