Selected Amino Acids Promote Mouse Pre-implantation Embryo Development in a Growth Factor-Like Manner.

L-Glutamine L-Proline amino acids blastocyst development hatching low-density culture pre-implantation embryo

Journal

Frontiers in physiology
ISSN: 1664-042X
Titre abrégé: Front Physiol
Pays: Switzerland
ID NLM: 101549006

Informations de publication

Date de publication:
2020
Historique:
received: 07 08 2019
accepted: 11 02 2020
entrez: 27 3 2020
pubmed: 27 3 2020
medline: 27 3 2020
Statut: epublish

Résumé

Groups of amino acids, and some selected amino acids, added to media used for culture of pre-implantation embryos have previously been shown to improve development in various ways including survival to the blastocyst stage, increased blastocyst cell number and improved hatching. In this study, we cultured 1-cell mouse embryos for 5 days to the hatching blastocyst stage in isosmotic medium (270 mOsm/kg) at high density (10 embryos/10 μL), where autocrine/paracrine support of development occurs, and low density (1 embryo/100 μL), where autocrine/paracrine support is minimized and development is compromised. When 400 μM L-Pro or 1 mM L-Gln was added to embryos at low density, the percentage of embryos reaching the blastocyst stage and the percentage hatching increased compared to low-density culture without these amino acids, and were now similar to those for embryos cultured at high density without amino acids. When L-Pro or L-Gln was added to embryos at high density, the percentage of embryos reaching the blastocyst stage didn't change but hatching improved. Neither embryo culture density nor the presence of these amino acids had any effect on blastocyst cell number. D-Pro and the osmolytes Gly and Betaine did not improve embryo development in low- or high-density culture indicating the mechanism was stereospecific and not osmotic, respectively. L-Pro- and L-Gln-mediated improvement in development is observed from the 5-cell stage and persists to the blastocyst stage. Molar excess of Gly, Betaine or L-Leu over L-Pro eliminated improvement in development and hatching consistent with them acting as competitive inhibitors of transporter-mediated uptake across the plasma membrane. The L-Pro effect is dependent on mTORC1 signaling (rapamycin sensitive) while that for L-Gln is not. The addition of L-Pro leads to significant nuclear translocation of p-Akt

Identifiants

pubmed: 32210831
doi: 10.3389/fphys.2020.00140
pmc: PMC7076138
doi:

Types de publication

Journal Article

Langues

eng

Pagination

140

Informations de copyright

Copyright © 2020 Morris, Ozsoy, Zada, Zada, Zamfirescu, Todorova and Day.

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Auteurs

Michael B Morris (MB)

Discipline of Physiology, School of Medical Sciences, The University of Sydney, Sydney, NSW, Australia.
Bosch Institute, The University of Sydney, Sydney, NSW, Australia.

Sukran Ozsoy (S)

Discipline of Physiology, School of Medical Sciences, The University of Sydney, Sydney, NSW, Australia.
Bosch Institute, The University of Sydney, Sydney, NSW, Australia.

Matthew Zada (M)

Discipline of Physiology, School of Medical Sciences, The University of Sydney, Sydney, NSW, Australia.
Bosch Institute, The University of Sydney, Sydney, NSW, Australia.

Mark Zada (M)

Discipline of Physiology, School of Medical Sciences, The University of Sydney, Sydney, NSW, Australia.
Bosch Institute, The University of Sydney, Sydney, NSW, Australia.

Radu C Zamfirescu (RC)

Discipline of Physiology, School of Medical Sciences, The University of Sydney, Sydney, NSW, Australia.
Bosch Institute, The University of Sydney, Sydney, NSW, Australia.

Mariana G Todorova (MG)

Discipline of Physiology, School of Medical Sciences, The University of Sydney, Sydney, NSW, Australia.
Bosch Institute, The University of Sydney, Sydney, NSW, Australia.

Margot L Day (ML)

Discipline of Physiology, School of Medical Sciences, The University of Sydney, Sydney, NSW, Australia.
Bosch Institute, The University of Sydney, Sydney, NSW, Australia.

Classifications MeSH