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CERVINO SIGNED

Can human embryo-released extracellular vesicles govern endometrial receptivity and inform on vanguard embryo diagnostics and fertility therapeutics?

Total Cost €

0

EC-Contrib. €

0

Partnership

0

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 CERVINO project word cloud

Explore the words cloud of the CERVINO project. It provides you a very rough idea of what is the project "CERVINO" about.

preimplantation    controversial    compromise    throughput    evs    function    single    screening    cargo    whereby    profile    uterine    endometrial    pilot    sequencing    genome    first    reported    therapeutic    biopsy    prior    exported    biosafety    introduce    vitro    genetic    pgs    pathophysiology    tackle    characterise    establishment    consequently    human    transcriptomic    negate    euploid    internalised    aneuploid    collectively    group    innovators    additionally    host    ivf    potentially    transfer    instead    demonstrated    quality    select    transcriptome    mount    extracellular    utilising    mechanistic    release    consequence    scrutinise    biopsies    material    cutting    poor    receptivity    delineating    inspire    edge    biomarkers    rnaseq    embryo    therapeutics    acquisition    utilised    paramount    embryos    genes    time    abundance    fertilisation    upregulation    cell    primary    internalisation    functional    revealed    invasive    had    implantation    cells    gene    screen    methodology    ecs    harmful    potentiates    effect    community    showed    natural    vesicles    ev   

Project "CERVINO" data sheet

The following table provides information about the project.

Coordinator
OSPEDALE SAN RAFFAELE SRL 

Organization address
address: VIA OLGETTINA 60
city: MILANO
postcode: 20132
website: www.hsr.it

contact info
title: n.a.
name: n.a.
surname: n.a.
function: n.a.
email: n.a.
telephone: n.a.
fax: n.a.

 Coordinator Country Italy [IT]
 Total cost 180˙277 €
 EC max contribution 180˙277 € (100%)
 Programme 1. H2020-EU.1.3.2. (Nurturing excellence by means of cross-border and cross-sector mobility)
 Code Call H2020-MSCA-IF-2017
 Funding Scheme MSCA-IF-EF-SE
 Starting year 2018
 Duration (year-month-day) from 2018-07-02   to  2020-07-01

 Partnership

Take a look of project's partnership.

# participants  country  role  EC contrib. [€] 
1    OSPEDALE SAN RAFFAELE SRL IT (MILANO) coordinator 180˙277.00

Map

 Project objective

Preimplantation Genetic Screening (PGS) based on high-throughput embryo genome sequencing is currently utilised in In Vitro Fertilisation (IVF) to select for euploid embryos prior to uterine transfer in order to increase implantation potential. The methodology for the acquisition of genetic material is controversial, as the invasive embryo biopsy required for PGS may compromise embryo quality. Moreover its long-term biosafety has not been evaluated. Consequently, the development of non-invasive methods to screen out aneuploid embryos is paramount. The host research group recently first reported that human IVF embryos release extracellular vesicles (EVs) and demonstrated their uptake by primary endometrial cells (ECs). Our pilot analysis of the embryo-derived EV transcriptome revealed an abundance of genes that may be involved in the establishment of endometrial receptivity. Additionally, our RNAseq on ECs, which had internalised human embryo-exported EVs, showed a gene-upregulation profile relevant to implantation. Collectively, our findings introduce a novel concept to the state-of-the-art whereby human embryos deliver a functional EV-transcriptomic cargo to ECs to mount an implantation response. Delineating the EV transcriptome, and studying the consequence of its delivery in ECs, potentiates mechanistic insight into the pathophysiology of implantation. The project will characterise for the first time the transcriptomic cargo of euploid and aneuploid human embryo-exported EVs and scrutinise the effect of its internalisation on endometrial function. This cutting-edge work may negate potentially harmful invasive embryo biopsies for PGS by instead utilising biomarkers in EVs – a ‘natural cell biopsy’. EV biomarkers could also inspire therapeutics to enhance endometrial receptivity. This programme is especially timely, as leading innovators in the field currently focus to provide the community with a single therapeutic approach to tackle poor endometrial function.

 Publications

year authors and title journal last update
List of publications.
2018 Sofia Makieva, Elisa Giacomini, Jessica Ottolina, Ana Sanchez, Enrico Papaleo, Paola Viganò
Inside the Endometrial Cell Signaling Subway: Mind the Gap(s)
published pages: 2477, ISSN: 1422-0067, DOI: 10.3390/ijms19092477
International Journal of Molecular Sciences 19/9 2019-06-11

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