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OVO-GROWTH SIGNED

Oogenesis spotlighted: making mature human oocytes

Total Cost €

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EC-Contrib. €

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Partnership

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 OVO-GROWTH project word cloud

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

niche    therapy    fail    eggs    networks    reveal    postnatal    mathematical    adulthood    transcriptional    ethical    fertility    conceive    mouse    survive    signalling    thousands    biopsies    netherlands    patient    maturation    expertise    hours    latest    profile    mice    cryopreserve    thereafter    risk    algorithms    xenotransplantation    toxicology    cellular    worldwide    systematically    perform    trajectories    single    follicular    foetal    reintroducing    malignancies    cancer    age    damaged    alternatives    somatic    successful    oocytes    material    humans    efficient    cell    plan    drop    vivo    disease    outcomes    patients    human    ovarian    engineer    counterparts    transplantation    mini    ovary    explore    vitro    too    autologous    oocyte    cells    later    cortical    life    profiling    personalized    gonadotoxic    preservation    gametogenesis    tissue    assays    reproductive    hematopoietic    childhood    follicle    graft    benchmark    molecular    mechanisms    organoid    sequenced    oogenesis    model    pregnancies    strips    chemotherapy    approval    identities    women    rare    breakthrough    possibility    led    seq    developmental   

Project "OVO-GROWTH" data sheet

The following table provides information about the project.

Coordinator
ACADEMISCH ZIEKENHUIS LEIDEN 

Organization address
address: ALBINUSDREEF 2
city: LEIDEN
postcode: 2333 ZA
website: www.lumc.nl

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 Netherlands [NL]
 Total cost 2˙000˙000 €
 EC max contribution 2˙000˙000 € (100%)
 Programme 1. H2020-EU.1.1. (EXCELLENT SCIENCE - European Research Council (ERC))
 Code Call ERC-2016-COG
 Funding Scheme ERC-COG
 Starting year 2017
 Duration (year-month-day) from 2017-07-01   to  2022-06-30

 Partnership

Take a look of project's partnership.

# participants  country  role  EC contrib. [€] 
1    ACADEMISCH ZIEKENHUIS LEIDEN NL (LEIDEN) coordinator 2˙000˙000.00

Map

 Project objective

Women who survive childhood cancer often fail to conceive because their eggs are damaged by (gonadotoxic) chemotherapy. A major breakthrough has been the possibility to cryopreserve cortical strips of their ovarian tissue for autologous transplantation later in life. This has led to over 40 successful pregnancies worldwide, the latest in the Netherlands. However, the risk of reintroducing cancer cells with the ovarian graft in patients with previous hematopoietic malignancies is too great and alternatives are needed. Here, I propose to build on my expertise in gametogenesis in mice and humans and perform a detailed study of the cellular networks and molecular pathways that control development and maturation of the oocyte within the human ovary. We have access and ethical approval for research on human foetal tissue and postnatal ovarian biopsies over a wide age range. I will use this rare material to systematically benchmark the transcriptional profile of cells in the human ovary (oocytes as well as somatic cells) during development and adulthood using Drop-seq, a novel cost-efficient single-cell technology that allows the profiling of thousands of cells in a matter of hours. Thereafter, we will apply mathematical algorithms to reveal cellular identities, developmental trajectories and signalling networks that control oogenesis. With this knowledge, I plan to engineer a human follicular niche creating a “mini-ovary” in vitro that could support the formation and maturation of the oocyte (using patient-specific cells) and to explore mechanisms of follicle maturation through a xenotransplantation mouse model. The cellular outcomes of these assays will be sequenced using Drop-seq and directly compared to their in vivo counterparts. Our approach will lead to more effective personalized-therapy for fertility preservation and contribute to the development of an in vitro mini-ovary organoid model to use in human reproductive toxicology and disease modelling.

 Publications

year authors and title journal last update
List of publications.
2019 X. Fan, M. Bialecka, I. Moustakas, E. Lam, V. Torrens-Juaneda, N. V. Borggreven, L. Trouw, L. A. Louwe, G. S. K. Pilgram, H. Mei, L. van der Westerlaken, S. M. Chuva de Sousa Lopes
Single-cell reconstruction of follicular remodeling in the human adult ovary
published pages: , ISSN: 2041-1723, DOI: 10.1038/s41467-019-11036-9
Nature Communications 10/1 2020-01-29
2018 Ábel Vértesy, Wibowo Arindrarto, Matthias S. Roost, Björn Reinius, Vanessa Torrens-Juaneda, Monika Bialecka, Ioannis Moustakas, Yavuz Ariyurek, Ewart Kuijk, Hailiang Mei, Rickard Sandberg, Alexander van Oudenaarden, Susana M. Chuva de Sousa Lopes
Parental haplotype-specific single-cell transcriptomics reveal incomplete epigenetic reprogramming in human female germ cells
published pages: na, ISSN: 2041-1723, DOI: 10.1038/s41467-018-04215-7
Nature Communications 9/1 2019-05-27
2017 Maria Gomes Fernandes, Nannan He, Fang Wang, Liesbeth Van Iperen, Cristina Eguizabal, Roberto Matorras, Bernard A J Roelen, Susana M Chuva De Sousa Lopes
Human-specific subcellular compartmentalization of P-element induced wimpy testis-like (PIWIL) granules during germ cell development and spermatogenesis
published pages: 258-269, ISSN: 0268-1161, DOI: 10.1093/humrep/dex365
Human Reproduction 33/2 2019-03-12
2018 Maria Gomes Fernandes, Monika Bialecka, Daniela C F Salvatori, Susana M Chuva de Sousa Lopes
Characterization of migratory primordial germ cells in the aorta-gonad-mesonephros of a 4.5-week-old human embryo: a toolbox to evaluate in vitro early gametogenesis
published pages: 233-243, ISSN: 1460-2407, DOI: 10.1093/molehr/gay011
MHR: Basic science of reproductive medicine 24/5 2019-03-12

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