Maternal spindle transfer overcomes embryo developmental arrest caused by ooplasmic defects in mice.

Infertility Spindle transfer cell biology developmental biology embryo development heteroplasmy mitochondrial DNA mouse oocytes

Journal

eLife
ISSN: 2050-084X
Titre abrégé: Elife
Pays: England
ID NLM: 101579614

Informations de publication

Date de publication:
29 04 2020
Historique:
received: 20 05 2019
accepted: 29 04 2020
pubmed: 30 4 2020
medline: 30 3 2021
entrez: 30 4 2020
Statut: epublish

Résumé

The developmental potential of early embryos is mainly dictated by the quality of the oocyte. Here, we explore the utility of the maternal spindle transfer (MST) technique as a reproductive approach to enhance oocyte developmental competence. Our proof-of-concept experiments show that replacement of the entire cytoplasm of oocytes from a sensitive mouse strain overcomes massive embryo developmental arrest characteristic of non-manipulated oocytes. Genetic analysis confirmed minimal carryover of mtDNA following MST. Resulting mice showed low heteroplasmy levels in multiple organs at adult age, normal histology and fertility. Mice were followed for five generations (F5), revealing that heteroplasmy was reduced in F2 mice and was undetectable in the subsequent generations. This pre-clinical model demonstrates the high efficiency and potential of the MST technique, not only to prevent the transmission of mtDNA mutations, but also as a new potential treatment for patients with certain forms of infertility refractory to current clinical strategies. Infertility is a growing problem that affects millions of people worldwide. Medical procedures known as in vitro fertilization (IVF) help many individuals experiencing infertility to have children. Typically in IVF, a woman’s egg cells are collected, fertilized with sperm from a chosen male and grown for a few days in a laboratory, before returning them to the woman’s body to continue to develop. However, there are some women whose egg cells cannot develop into a healthy baby after they have been fertilized. Many of these patients use egg cells from donors, instead. This greatly improves the chances of the IVF treatment being successful, but the resultant children are not genetically related to the intended mothers. Previous studies suggested that a cell compartment known as the cytoplasm plays a crucial role in allowing fertilized egg cells to develop normally. A new technique known as maternal spindle transfer, often shortened to MST, makes it possible to replace the entire cytoplasm of a compromised egg cell. This is achieved by transplanting the genetic material of the compromised egg cell into a donor egg cell with healthier cytoplasm that has previously had its own genetic material removed. Using this technique, it is possible to generate human egg cells for IVF that have the genetic material from the intended mother without the defects in the cytoplasm that may be responsible for infertility. However, it is not clear whether this approach would be a safe and effective way to treat infertility in humans. Costa-Borges et al. applied MST to infertile female mice and found that the technique could permanently correct deficiencies in the cytoplasms of poor quality egg cells, allowing the mice to give birth to healthy offspring. Further experiments studied the offspring and their descendants over several generations and found that they also had higher quality egg cells and normal levels of fertility. These findings open up the possibility of developing new treatments for infertility caused by problems with egg cells, so experiments involving human egg cells are now being performed to evaluate the safety and effectiveness of the technique.

Autres résumés

Type: plain-language-summary (eng)
Infertility is a growing problem that affects millions of people worldwide. Medical procedures known as in vitro fertilization (IVF) help many individuals experiencing infertility to have children. Typically in IVF, a woman’s egg cells are collected, fertilized with sperm from a chosen male and grown for a few days in a laboratory, before returning them to the woman’s body to continue to develop. However, there are some women whose egg cells cannot develop into a healthy baby after they have been fertilized. Many of these patients use egg cells from donors, instead. This greatly improves the chances of the IVF treatment being successful, but the resultant children are not genetically related to the intended mothers. Previous studies suggested that a cell compartment known as the cytoplasm plays a crucial role in allowing fertilized egg cells to develop normally. A new technique known as maternal spindle transfer, often shortened to MST, makes it possible to replace the entire cytoplasm of a compromised egg cell. This is achieved by transplanting the genetic material of the compromised egg cell into a donor egg cell with healthier cytoplasm that has previously had its own genetic material removed. Using this technique, it is possible to generate human egg cells for IVF that have the genetic material from the intended mother without the defects in the cytoplasm that may be responsible for infertility. However, it is not clear whether this approach would be a safe and effective way to treat infertility in humans. Costa-Borges et al. applied MST to infertile female mice and found that the technique could permanently correct deficiencies in the cytoplasms of poor quality egg cells, allowing the mice to give birth to healthy offspring. Further experiments studied the offspring and their descendants over several generations and found that they also had higher quality egg cells and normal levels of fertility. These findings open up the possibility of developing new treatments for infertility caused by problems with egg cells, so experiments involving human egg cells are now being performed to evaluate the safety and effectiveness of the technique.

Identifiants

pubmed: 32347793
doi: 10.7554/eLife.48591
pii: 48591
pmc: PMC7259950
doi:
pii:

Substances chimiques

DNA, Mitochondrial 0

Types de publication

Journal Article Research Support, N.I.H., Extramural Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Subventions

Organisme : European Regional Development Fund
ID : RD-15-1-0011
Pays : International
Organisme : NIH HHS
ID : 1R01HD092550-01
Pays : United States

Informations de copyright

© 2020, Costa-Borges et al.

Déclaration de conflit d'intérêts

NC, KS, IM, EM, RB, AS, MG, IV, JG, KR, DW, GC No competing interests declared

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Auteurs

Nuno Costa-Borges (N)

Embryotools, Parc Cientific de Barcelona, Barcelona, Spain.

Katharina Spath (K)

Nuffield Department of Women's and Reproductive Health, University of Oxford, Oxford, United Kingdom.
Juno Genetics, Winchester House, Oxford Science Park, Oxford, United Kingdom.

Irene Miguel-Escalada (I)

Genomics and Bioinformatics, Centre for Genomic Regulation, Barcelona, Spain.

Enric Mestres (E)

Embryotools, Parc Cientific de Barcelona, Barcelona, Spain.

Rosa Balmaseda (R)

PCB Animal Facility, Parc Cientific de Barcelona, Barcelona, Spain.

Anna Serafín (A)

PCB Animal Facility, Parc Cientific de Barcelona, Barcelona, Spain.

Maria Garcia-Jiménez (M)

Embryotools, Parc Cientific de Barcelona, Barcelona, Spain.

Ivette Vanrell (I)

Embryotools, Parc Cientific de Barcelona, Barcelona, Spain.

Jesús González (J)

PCB Animal Facility, Parc Cientific de Barcelona, Barcelona, Spain.

Klaus Rink (K)

Embryotools, Parc Cientific de Barcelona, Barcelona, Spain.

Dagan Wells (D)

Nuffield Department of Women's and Reproductive Health, University of Oxford, Oxford, United Kingdom.
Juno Genetics, Winchester House, Oxford Science Park, Oxford, United Kingdom.

Gloria Calderón (G)

Embryotools, Parc Cientific de Barcelona, Barcelona, Spain.

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