Effect of stem cell activation, culture media of manipulated embryos, and site of embryo transfer in the production of F0 embryonic stem cell mice

Recently, F0 embryonic stem (ES) cell mice have been produced by injection of ES cells into eight-cell embryos using either laser- or piezo-assisted injection systems. To simplify the injection procedure, we have optimized the conventional blastocyst injection method, free of laser- or piezo-assisted micromanipulation systems, to produce F0 ES cell pups. To increase the efficiency of producing mice from ES cell injection into eight-cell and blastocyst stage embryos, we have tested 1) the effect of activating ES cell before injection, 2) the effect of in vitro culture in medium optimized for the survival of both ES cells and embryos, and 3) the effect of transferring the micromanipulated embryos into the oviduct versus into the uterus of CD1 foster mice. Two B6D2 hybrid ES cell lines were used for injection in a multifactorial analysis to evaluate the efficiency of producing live chimeric and F0 ES cell mice. Our results demonstrate that the activation of ES cells and the appropriate culture conditions are crucial parameters influencing the generation of F0 ES cell offspring. Transfer of blastocysts injected with ES cells into the oviduct of 0.5-day postcoitum pseudopregnant females increased the number of live animals with higher chimera proportion. Under these conditions, injections into eight-cell embryos produce a high number of F0 ES mice, and the conventional blastocyst injection method produces a lower number of F0 ES cell pups; however, the efficiency of production of chimeric mice with germline transmission was high. We have developed an economical and efficient technique for producing fully ES cell-derived F0 mice with full germline transmission that can be applied in many laboratories without the use of piezo or laser instruments. © 2009 by the Society for the Study of Reproduction, Inc.

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Main Authors: Ramírez De Paz, Miguel Ángel, Fernández González, Raúl, Pérez-Crespo, M., Pericuesta Camacho, Eva, Gutiérrez Adán, Alfonso
Format: artículo biblioteca
Language:English
Published: Oxford University Press  2009
Subjects:Cell activation, Culture media, Embryo transfer, Embryonic stem cell, Mouse,
Online Access:http://hdl.handle.net/20.500.12792/3622
http://hdl.handle.net/10261/292340
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spelling dig-inia-es-10261-2923402023-02-20T07:27:56Z Effect of stem cell activation, culture media of manipulated embryos, and site of embryo transfer in the production of F0 embryonic stem cell mice Ramírez De Paz, Miguel Ángel Fernández González, Raúl Pérez-Crespo, M. Pericuesta Camacho, Eva Gutiérrez Adán, Alfonso Cell activation Culture media Embryo transfer Embryonic stem cell Mouse Recently, F0 embryonic stem (ES) cell mice have been produced by injection of ES cells into eight-cell embryos using either laser- or piezo-assisted injection systems. To simplify the injection procedure, we have optimized the conventional blastocyst injection method, free of laser- or piezo-assisted micromanipulation systems, to produce F0 ES cell pups. To increase the efficiency of producing mice from ES cell injection into eight-cell and blastocyst stage embryos, we have tested 1) the effect of activating ES cell before injection, 2) the effect of in vitro culture in medium optimized for the survival of both ES cells and embryos, and 3) the effect of transferring the micromanipulated embryos into the oviduct versus into the uterus of CD1 foster mice. Two B6D2 hybrid ES cell lines were used for injection in a multifactorial analysis to evaluate the efficiency of producing live chimeric and F0 ES cell mice. Our results demonstrate that the activation of ES cells and the appropriate culture conditions are crucial parameters influencing the generation of F0 ES cell offspring. Transfer of blastocysts injected with ES cells into the oviduct of 0.5-day postcoitum pseudopregnant females increased the number of live animals with higher chimera proportion. Under these conditions, injections into eight-cell embryos produce a high number of F0 ES mice, and the conventional blastocyst injection method produces a lower number of F0 ES cell pups; however, the efficiency of production of chimeric mice with germline transmission was high. We have developed an economical and efficient technique for producing fully ES cell-derived F0 mice with full germline transmission that can be applied in many laboratories without the use of piezo or laser instruments. © 2009 by the Society for the Study of Reproduction, Inc. 2023-02-20T07:27:56Z 2023-02-20T07:27:56Z 2009 artículo Biology of Reproduction 80: 1216-1222 (2009) 0006-3363 http://hdl.handle.net/20.500.12792/3622 http://hdl.handle.net/10261/292340 10.1095/biolreprod.108.075044 1259-7268 en none Oxford University Press 
institution INIA ES
collection DSpace
country España
countrycode ES
component Bibliográfico
access En linea
databasecode dig-inia-es
tag biblioteca
region Europa del Sur
libraryname Biblioteca del INIA España
language English
topic Cell activation
Culture media
Embryo transfer
Embryonic stem cell
Mouse
Cell activation
Culture media
Embryo transfer
Embryonic stem cell
Mouse
spellingShingle Cell activation
Culture media
Embryo transfer
Embryonic stem cell
Mouse
Cell activation
Culture media
Embryo transfer
Embryonic stem cell
Mouse
Ramírez De Paz, Miguel Ángel
Fernández González, Raúl
Pérez-Crespo, M.
Pericuesta Camacho, Eva
Gutiérrez Adán, Alfonso
Effect of stem cell activation, culture media of manipulated embryos, and site of embryo transfer in the production of F0 embryonic stem cell mice
description Recently, F0 embryonic stem (ES) cell mice have been produced by injection of ES cells into eight-cell embryos using either laser- or piezo-assisted injection systems. To simplify the injection procedure, we have optimized the conventional blastocyst injection method, free of laser- or piezo-assisted micromanipulation systems, to produce F0 ES cell pups. To increase the efficiency of producing mice from ES cell injection into eight-cell and blastocyst stage embryos, we have tested 1) the effect of activating ES cell before injection, 2) the effect of in vitro culture in medium optimized for the survival of both ES cells and embryos, and 3) the effect of transferring the micromanipulated embryos into the oviduct versus into the uterus of CD1 foster mice. Two B6D2 hybrid ES cell lines were used for injection in a multifactorial analysis to evaluate the efficiency of producing live chimeric and F0 ES cell mice. Our results demonstrate that the activation of ES cells and the appropriate culture conditions are crucial parameters influencing the generation of F0 ES cell offspring. Transfer of blastocysts injected with ES cells into the oviduct of 0.5-day postcoitum pseudopregnant females increased the number of live animals with higher chimera proportion. Under these conditions, injections into eight-cell embryos produce a high number of F0 ES mice, and the conventional blastocyst injection method produces a lower number of F0 ES cell pups; however, the efficiency of production of chimeric mice with germline transmission was high. We have developed an economical and efficient technique for producing fully ES cell-derived F0 mice with full germline transmission that can be applied in many laboratories without the use of piezo or laser instruments. © 2009 by the Society for the Study of Reproduction, Inc.
format artículo
topic_facet Cell activation
Culture media
Embryo transfer
Embryonic stem cell
Mouse
author Ramírez De Paz, Miguel Ángel
Fernández González, Raúl
Pérez-Crespo, M.
Pericuesta Camacho, Eva
Gutiérrez Adán, Alfonso
author_facet Ramírez De Paz, Miguel Ángel
Fernández González, Raúl
Pérez-Crespo, M.
Pericuesta Camacho, Eva
Gutiérrez Adán, Alfonso
author_sort Ramírez De Paz, Miguel Ángel
title Effect of stem cell activation, culture media of manipulated embryos, and site of embryo transfer in the production of F0 embryonic stem cell mice
title_short Effect of stem cell activation, culture media of manipulated embryos, and site of embryo transfer in the production of F0 embryonic stem cell mice
title_full Effect of stem cell activation, culture media of manipulated embryos, and site of embryo transfer in the production of F0 embryonic stem cell mice
title_fullStr Effect of stem cell activation, culture media of manipulated embryos, and site of embryo transfer in the production of F0 embryonic stem cell mice
title_full_unstemmed Effect of stem cell activation, culture media of manipulated embryos, and site of embryo transfer in the production of F0 embryonic stem cell mice
title_sort effect of stem cell activation, culture media of manipulated embryos, and site of embryo transfer in the production of f0 embryonic stem cell mice
publisher Oxford University Press 
publishDate 2009
url http://hdl.handle.net/20.500.12792/3622
http://hdl.handle.net/10261/292340
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