Proline and Proline Analogues Improve Development of Mouse Preimplantation Embryos by Protecting Them against Oxidative Stress

The culture of embryos in the non-essential amino acid L-proline (Pro) or its analogues pipecolic acid (PA) and L-4-thiazolidine carboxylic acid (L4T) improves embryo development, increasing the percentage that develop to the blastocyst stage and hatch. Staining of 2-cell and 4-cell embryos with tet...

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Main Authors: Madeleine L. M. Hardy, Dheerja Lakhiani, Michael B. Morris, Margot L. Day
Format: Article
Language:English
Published: MDPI AG 2023-11-01
Series:Cells
Subjects:
Online Access:https://www.mdpi.com/2073-4409/12/22/2640
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author Madeleine L. M. Hardy
Dheerja Lakhiani
Michael B. Morris
Margot L. Day
author_facet Madeleine L. M. Hardy
Dheerja Lakhiani
Michael B. Morris
Margot L. Day
author_sort Madeleine L. M. Hardy
collection DOAJ
description The culture of embryos in the non-essential amino acid L-proline (Pro) or its analogues pipecolic acid (PA) and L-4-thiazolidine carboxylic acid (L4T) improves embryo development, increasing the percentage that develop to the blastocyst stage and hatch. Staining of 2-cell and 4-cell embryos with tetramethylrhodamine methyl ester and 2′,7′-dichlorofluorescein diacetate showed that the culture of embryos in the presence of Pro, or either of these analogues, reduced mitochondrial activity and reactive oxygen species (ROS), respectively, indicating potential mechanisms by which embryo development is improved. Inhibition of the Pro metabolism enzyme, proline oxidase, by tetrahydro-2-furoic-acid prevented these reductions and concomitantly prevented the improved development. The ways in which Pro, PA and L4T reduce mitochondrial activity and ROS appear to differ, despite their structural similarity. Specifically, the results are consistent with Pro reducing ROS by reducing mitochondrial activity while PA and L4T may be acting as ROS scavengers. All three may work to reduce ROS by contributing to the GSH pool. Overall, our results indicate that reduction in mitochondrial activity and oxidative stress are potential mechanisms by which Pro and its analogues act to improve pre-implantation embryo development.
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spelling doaj.art-f5efb69d0d8a462281f7a256e4fa28c02023-11-24T14:35:26ZengMDPI AGCells2073-44092023-11-011222264010.3390/cells12222640Proline and Proline Analogues Improve Development of Mouse Preimplantation Embryos by Protecting Them against Oxidative StressMadeleine L. M. Hardy0Dheerja Lakhiani1Michael B. Morris2Margot L. Day3School of Medical Sciences, Faculty of Medicine and Health, The University of Sydney, Sydney, NSW 2006, AustraliaSchool of Medical Sciences, Faculty of Medicine and Health, The University of Sydney, Sydney, NSW 2006, AustraliaSchool of Medical Sciences, Faculty of Medicine and Health, The University of Sydney, Sydney, NSW 2006, AustraliaSchool of Medical Sciences, Faculty of Medicine and Health, The University of Sydney, Sydney, NSW 2006, AustraliaThe culture of embryos in the non-essential amino acid L-proline (Pro) or its analogues pipecolic acid (PA) and L-4-thiazolidine carboxylic acid (L4T) improves embryo development, increasing the percentage that develop to the blastocyst stage and hatch. Staining of 2-cell and 4-cell embryos with tetramethylrhodamine methyl ester and 2′,7′-dichlorofluorescein diacetate showed that the culture of embryos in the presence of Pro, or either of these analogues, reduced mitochondrial activity and reactive oxygen species (ROS), respectively, indicating potential mechanisms by which embryo development is improved. Inhibition of the Pro metabolism enzyme, proline oxidase, by tetrahydro-2-furoic-acid prevented these reductions and concomitantly prevented the improved development. The ways in which Pro, PA and L4T reduce mitochondrial activity and ROS appear to differ, despite their structural similarity. Specifically, the results are consistent with Pro reducing ROS by reducing mitochondrial activity while PA and L4T may be acting as ROS scavengers. All three may work to reduce ROS by contributing to the GSH pool. Overall, our results indicate that reduction in mitochondrial activity and oxidative stress are potential mechanisms by which Pro and its analogues act to improve pre-implantation embryo development.https://www.mdpi.com/2073-4409/12/22/2640mitochondrial activityoxidative stresspipecolic acidpre-implantation embryo developmentprolinereactive oxygen species
spellingShingle Madeleine L. M. Hardy
Dheerja Lakhiani
Michael B. Morris
Margot L. Day
Proline and Proline Analogues Improve Development of Mouse Preimplantation Embryos by Protecting Them against Oxidative Stress
Cells
mitochondrial activity
oxidative stress
pipecolic acid
pre-implantation embryo development
proline
reactive oxygen species
title Proline and Proline Analogues Improve Development of Mouse Preimplantation Embryos by Protecting Them against Oxidative Stress
title_full Proline and Proline Analogues Improve Development of Mouse Preimplantation Embryos by Protecting Them against Oxidative Stress
title_fullStr Proline and Proline Analogues Improve Development of Mouse Preimplantation Embryos by Protecting Them against Oxidative Stress
title_full_unstemmed Proline and Proline Analogues Improve Development of Mouse Preimplantation Embryos by Protecting Them against Oxidative Stress
title_short Proline and Proline Analogues Improve Development of Mouse Preimplantation Embryos by Protecting Them against Oxidative Stress
title_sort proline and proline analogues improve development of mouse preimplantation embryos by protecting them against oxidative stress
topic mitochondrial activity
oxidative stress
pipecolic acid
pre-implantation embryo development
proline
reactive oxygen species
url https://www.mdpi.com/2073-4409/12/22/2640
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AT michaelbmorris prolineandprolineanaloguesimprovedevelopmentofmousepreimplantationembryosbyprotectingthemagainstoxidativestress
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