Optimization of In Vitro Murine Embryo Culture Condition based on Commercial M16 Media

In vitro culture of murine embryos is an important step for in vitro production systems including in vitro fertilization and generations of genetically engineered mice. M16 is widely used commercialized culture media for the murine embryos. Compared to other media such as potassium simplex optimizat...

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Main Authors: Soo Jin Lee, Hee Sook Bae, Ok Jae Koo
Format: Article
Language:English
Published: The Korean Society of Animal Reproduction and Biotechnology 2015-12-01
Series:Journal of Animal Reproduction and Biotechnology
Subjects:
m16
Online Access:http://www.e-jarb.org/journal/view.html?uid=1501&vmd=Full
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spelling doaj-415d891bf11743b18dd42604bdbac0b62021-01-10T08:56:35ZengThe Korean Society of Animal Reproduction and BiotechnologyJournal of Animal Reproduction and Biotechnology2671-46392671-46632015-12-0130431531710.12750/JET.2015.30.4.315Optimization of In Vitro Murine Embryo Culture Condition based on Commercial M16 MediaSoo Jin Lee0Hee Sook Bae 1 Ok Jae Koo2Laboratory Animal Research Center, Samsung Biomedical Research Institute, Suwon 16419, Korea.Laboratory Animal Research Center, Samsung Biomedical Research Institute, Suwon 16419, Korea.Laboratory Animal Research Center, Samsung Biomedical Research Institute, Suwon 16419, KoreaIn vitro culture of murine embryos is an important step for in vitro production systems including in vitro fertilization and generations of genetically engineered mice. M16 is widely used commercialized culture media for the murine embryos. Compared to other media such as potassium simplex optimization medium, commercial M16 (Sigma) media lacks of amino acid, glutamine and antibiotics. In the present study, we optimized M16 based embryo culture system using commercialized antibiotics-glutamine or amino acids supplements. In vivo derived murine zygote were M16 media were supplemented with commercial Penicillin-Streptomycin-Glutamine solution (PSG; Gibco) or MEM Non- Essential Amino Acids solution (NEAA; Gibco) as experimental design. Addition of PSG did not improved cleavage and blastocyst rates. On the other hand, cleavage rate is not different between control and NEAA treated group, however, blastocyst formation is significantly (P<0.05) improved in NEAA treated group. Developmental competence between PSG and NEAA treated groups were also compared. Between two groups, cleavage rate was similar. However, blastocyst formation rate is significantly improved in NEAA treated group. Taken together, beneficial effect of NEAA on murine embryos development was confirmed. Effect of antibiotics and glutamine addition to M16 media is still not clear in the study.http://www.e-jarb.org/journal/view.html?uid=1501&vmd=Fullmouse embryoin vitro cultureneaam16
collection DOAJ
language English
format Article
sources DOAJ
author Soo Jin Lee
Hee Sook Bae
Ok Jae Koo
spellingShingle Soo Jin Lee
Hee Sook Bae
Ok Jae Koo
Optimization of In Vitro Murine Embryo Culture Condition based on Commercial M16 Media
Journal of Animal Reproduction and Biotechnology
mouse embryo
in vitro culture
neaa
m16
author_facet Soo Jin Lee
Hee Sook Bae
Ok Jae Koo
author_sort Soo Jin Lee
title Optimization of In Vitro Murine Embryo Culture Condition based on Commercial M16 Media
title_short Optimization of In Vitro Murine Embryo Culture Condition based on Commercial M16 Media
title_full Optimization of In Vitro Murine Embryo Culture Condition based on Commercial M16 Media
title_fullStr Optimization of In Vitro Murine Embryo Culture Condition based on Commercial M16 Media
title_full_unstemmed Optimization of In Vitro Murine Embryo Culture Condition based on Commercial M16 Media
title_sort optimization of in vitro murine embryo culture condition based on commercial m16 media
publisher The Korean Society of Animal Reproduction and Biotechnology
series Journal of Animal Reproduction and Biotechnology
issn 2671-4639
2671-4663
publishDate 2015-12-01
description In vitro culture of murine embryos is an important step for in vitro production systems including in vitro fertilization and generations of genetically engineered mice. M16 is widely used commercialized culture media for the murine embryos. Compared to other media such as potassium simplex optimization medium, commercial M16 (Sigma) media lacks of amino acid, glutamine and antibiotics. In the present study, we optimized M16 based embryo culture system using commercialized antibiotics-glutamine or amino acids supplements. In vivo derived murine zygote were M16 media were supplemented with commercial Penicillin-Streptomycin-Glutamine solution (PSG; Gibco) or MEM Non- Essential Amino Acids solution (NEAA; Gibco) as experimental design. Addition of PSG did not improved cleavage and blastocyst rates. On the other hand, cleavage rate is not different between control and NEAA treated group, however, blastocyst formation is significantly (P<0.05) improved in NEAA treated group. Developmental competence between PSG and NEAA treated groups were also compared. Between two groups, cleavage rate was similar. However, blastocyst formation rate is significantly improved in NEAA treated group. Taken together, beneficial effect of NEAA on murine embryos development was confirmed. Effect of antibiotics and glutamine addition to M16 media is still not clear in the study.
topic mouse embryo
in vitro culture
neaa
m16
url http://www.e-jarb.org/journal/view.html?uid=1501&vmd=Full
work_keys_str_mv AT soojinlee optimizationofinvitromurineembryocultureconditionbasedoncommercialm16media
AT heesookbae optimizationofinvitromurineembryocultureconditionbasedoncommercialm16media
AT okjaekoo optimizationofinvitromurineembryocultureconditionbasedoncommercialm16media
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