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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The Korean Society of Animal Reproduction and Biotechnology
2015-12-01
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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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