Chloroquine mitigates long-term effects of in vitro culture in mouse embryos

BackgroundIn vitro culture of preimplantation embryos may increase the risk of long-term effects, such as obesity and metabolic diseases later in life in the offspring. While the long-term consequences of low-protein diets during early development have been reported in the context of DOHaD (Developm...

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Main Authors: Kaname Sato, Itsuki Koide, Md Wasim Bari, Satoshi Kishigami
Format: Article
Language:English
Published: Frontiers Media S.A. 2025-08-01
Series:Frontiers in Cell and Developmental Biology
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Online Access:https://www.frontiersin.org/articles/10.3389/fcell.2025.1640986/full
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author Kaname Sato
Itsuki Koide
Md Wasim Bari
Satoshi Kishigami
Satoshi Kishigami
Satoshi Kishigami
author_facet Kaname Sato
Itsuki Koide
Md Wasim Bari
Satoshi Kishigami
Satoshi Kishigami
Satoshi Kishigami
author_sort Kaname Sato
collection DOAJ
description BackgroundIn vitro culture of preimplantation embryos may increase the risk of long-term effects, such as obesity and metabolic diseases later in life in the offspring. While the long-term consequences of low-protein diets during early development have been reported in the context of DOHaD (Developmental Origins of Health and Disease) theory, the relationship between nutrient supply via autophagy during preimplantation development and these long-term effects remains unclear. In this study, we aimed to determine whether autophagy activity during in vitro culture of mouse embryos contributes to long-term effects, using chloroquine (CQ), a known autophagy inhibitor. Preimplantation embryos were cultured in vitro in the presence of CQ. The purpose was to investigate the long-term consequences of nutrient deprivation during preimplantation development under conditions of autophagy inhibition.MethodsTwo-cell stage embryos were obtained by mating ICR female mice with ICR male mice, followed by oviduct flushing. The recovered embryos were cultured in vitro in CQ-supplemented medium. At the blastocyst stage, cultured embryos were immunostained with anti-Nanog and Cdx2 antibodies to assess blastocyst quality. Offspring derived from CQ-treated embryos were obtained by transferring the cultured embryos to pseudopregnant ICR females. At 8 weeks or later of age, offspring were examined using a glucose tolerance test.ResultsWe found that low concentration CQ significantly reduced developmental rate and total cell count in a CQ concentration-dependent manner (control: 67 ± 2.5 vs. 48 ± 2.3 with 1.0 µM CQ vs. 37 ± 2.9 with 2.0 µM CQ), as well as the numbers of trophectoderm (TE) and inner cell mass (ICM) cells. These results suggest that low concentration CQ treatment may suppress cell proliferation likely by inhibiting nutrient supply via autophagy. Notably, after implantation, the 2.0 µM CQ-treated group exhibited increased pups rate and reduced body weight comparable to the naturally mated group, and glucose tolerance similar to that of the naturally mated group, in contrasted to the untreated group.DiscussionThese findings suggest that inhibiting autophagy during preimplantation development may mitigate the long-term effects of in vitro culture and support normal postnatal growth and metabolism. Thus, autophagy activity in early development may be a key cellular process underlying long term effects observed at later stages.
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spelling doaj-art-4eeb751feb7e4572b973df4b068f9d852025-08-20T04:02:31ZengFrontiers Media S.A.Frontiers in Cell and Developmental Biology2296-634X2025-08-011310.3389/fcell.2025.16409861640986Chloroquine mitigates long-term effects of in vitro culture in mouse embryosKaname Sato0Itsuki Koide1Md Wasim Bari2Satoshi Kishigami3Satoshi Kishigami4Satoshi Kishigami5Department of Integrated Applied Life Science, Integrated Graduate School of Medicine, Engineering, and Agricultural Sciences, University of Yamanashi, Kofu, JapanDepartment of Integrated Applied Life Science, Integrated Graduate School of Medicine, Engineering, and Agricultural Sciences, University of Yamanashi, Kofu, JapanGraduate School of Life and Environmental Sciences, Integrated Graduate School of Medicine, Engineering, and Agricultural Sciences, University of Yamanashi, Kofu, JapanDepartment of Integrated Applied Life Science, Integrated Graduate School of Medicine, Engineering, and Agricultural Sciences, University of Yamanashi, Kofu, JapanGraduate School of Life and Environmental Sciences, Integrated Graduate School of Medicine, Engineering, and Agricultural Sciences, University of Yamanashi, Kofu, JapanCenter for advanced Assisted Reproductive Technologies, University of Yamanashi, Kofu, JapanBackgroundIn vitro culture of preimplantation embryos may increase the risk of long-term effects, such as obesity and metabolic diseases later in life in the offspring. While the long-term consequences of low-protein diets during early development have been reported in the context of DOHaD (Developmental Origins of Health and Disease) theory, the relationship between nutrient supply via autophagy during preimplantation development and these long-term effects remains unclear. In this study, we aimed to determine whether autophagy activity during in vitro culture of mouse embryos contributes to long-term effects, using chloroquine (CQ), a known autophagy inhibitor. Preimplantation embryos were cultured in vitro in the presence of CQ. The purpose was to investigate the long-term consequences of nutrient deprivation during preimplantation development under conditions of autophagy inhibition.MethodsTwo-cell stage embryos were obtained by mating ICR female mice with ICR male mice, followed by oviduct flushing. The recovered embryos were cultured in vitro in CQ-supplemented medium. At the blastocyst stage, cultured embryos were immunostained with anti-Nanog and Cdx2 antibodies to assess blastocyst quality. Offspring derived from CQ-treated embryos were obtained by transferring the cultured embryos to pseudopregnant ICR females. At 8 weeks or later of age, offspring were examined using a glucose tolerance test.ResultsWe found that low concentration CQ significantly reduced developmental rate and total cell count in a CQ concentration-dependent manner (control: 67 ± 2.5 vs. 48 ± 2.3 with 1.0 µM CQ vs. 37 ± 2.9 with 2.0 µM CQ), as well as the numbers of trophectoderm (TE) and inner cell mass (ICM) cells. These results suggest that low concentration CQ treatment may suppress cell proliferation likely by inhibiting nutrient supply via autophagy. Notably, after implantation, the 2.0 µM CQ-treated group exhibited increased pups rate and reduced body weight comparable to the naturally mated group, and glucose tolerance similar to that of the naturally mated group, in contrasted to the untreated group.DiscussionThese findings suggest that inhibiting autophagy during preimplantation development may mitigate the long-term effects of in vitro culture and support normal postnatal growth and metabolism. Thus, autophagy activity in early development may be a key cellular process underlying long term effects observed at later stages.https://www.frontiersin.org/articles/10.3389/fcell.2025.1640986/fullchloroquinein vitro culturemouse embryoautophagyDOHAD
spellingShingle Kaname Sato
Itsuki Koide
Md Wasim Bari
Satoshi Kishigami
Satoshi Kishigami
Satoshi Kishigami
Chloroquine mitigates long-term effects of in vitro culture in mouse embryos
Frontiers in Cell and Developmental Biology
chloroquine
in vitro culture
mouse embryo
autophagy
DOHAD
title Chloroquine mitigates long-term effects of in vitro culture in mouse embryos
title_full Chloroquine mitigates long-term effects of in vitro culture in mouse embryos
title_fullStr Chloroquine mitigates long-term effects of in vitro culture in mouse embryos
title_full_unstemmed Chloroquine mitigates long-term effects of in vitro culture in mouse embryos
title_short Chloroquine mitigates long-term effects of in vitro culture in mouse embryos
title_sort chloroquine mitigates long term effects of in vitro culture in mouse embryos
topic chloroquine
in vitro culture
mouse embryo
autophagy
DOHAD
url https://www.frontiersin.org/articles/10.3389/fcell.2025.1640986/full
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AT itsukikoide chloroquinemitigateslongtermeffectsofinvitrocultureinmouseembryos
AT mdwasimbari chloroquinemitigateslongtermeffectsofinvitrocultureinmouseembryos
AT satoshikishigami chloroquinemitigateslongtermeffectsofinvitrocultureinmouseembryos
AT satoshikishigami chloroquinemitigateslongtermeffectsofinvitrocultureinmouseembryos
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