Embryonic stem cells in pig and cattle: derivation, culture and potential applications

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Standard

Embryonic stem cells in pig and cattle : derivation, culture and potential applications. / Maddox-Hyttel, Poul; Wolf, Xenia Asbæk; Rasmussen, Mikkel Aabech; Schauser, Kirsten.

I: Acta Scientiae Veterinariae, Bind 35, Nr. Suppl. 3, 2007, s. s823-s830.

Publikation: Bidrag til tidsskriftTidsskriftartikelForskningfagfællebedømt

Harvard

Maddox-Hyttel, P, Wolf, XA, Rasmussen, MA & Schauser, K 2007, 'Embryonic stem cells in pig and cattle: derivation, culture and potential applications', Acta Scientiae Veterinariae, bind 35, nr. Suppl. 3, s. s823-s830.

APA

Maddox-Hyttel, P., Wolf, X. A., Rasmussen, M. A., & Schauser, K. (2007). Embryonic stem cells in pig and cattle: derivation, culture and potential applications. Acta Scientiae Veterinariae, 35(Suppl. 3), s823-s830.

Vancouver

Maddox-Hyttel P, Wolf XA, Rasmussen MA, Schauser K. Embryonic stem cells in pig and cattle: derivation, culture and potential applications. Acta Scientiae Veterinariae. 2007;35(Suppl. 3):s823-s830.

Author

Maddox-Hyttel, Poul ; Wolf, Xenia Asbæk ; Rasmussen, Mikkel Aabech ; Schauser, Kirsten. / Embryonic stem cells in pig and cattle : derivation, culture and potential applications. I: Acta Scientiae Veterinariae. 2007 ; Bind 35, Nr. Suppl. 3. s. s823-s830.

Bibtex

@article{b9ddc870a1c211ddb6ae000ea68e967b,
title = "Embryonic stem cells in pig and cattle: derivation, culture and potential applications",
abstract = "Porcine and bovine cell lines derived from the inner cell mass (ICM) or epiblasts of blastocysts have been maintained over extended periods of time and characterized by morphology, identification of some stem cell markers and, in few cases, by production of chimaeric offspring. However, germ line transmission in chimaeras has never been obtained. Due to this incomplete characterization of the cell lines, the expression embryonic stem (ES)-like cells is presently used in pig and cattle. The ICM or epiblast can be isolated from the blastocyst by whole blastocyst culture, mechanical isolation, or immunosurgery, and they are generally cultured on feeder cells. The resulting ES-like cells may be differentiated in vivo by chimaera and teratoma formation or in vitro by embryoid body formation and monolayer induction. It is likely that more well characterized and stable porcine and bovine ES cell lines will be available over the coming years. However, in order to reach this goal further systematic research is needed. Such cell lines hold promises for developing adequate models for human ES cell therapy and they may open for new avenues for the production of genetically modified animals as the ES cells ahve indefinite selfrenewal capacity and may be more prone for homologous recombination. Finally, ES cell lines established from blastocysts, which are genetically modified to carry human disease genes, may be differentiated into particular cell populations that may allow for studies of disease mechanisms at the cellular level in vitro as a parallel to studies on whole animal models born from transfer of similar genetically modified embryos.",
keywords = "Former LIFE faculty, Embryonic stem cells, pig, cattle, pluripotency, differentiation",
author = "Poul Maddox-Hyttel and Wolf, {Xenia Asb{\ae}k} and Rasmussen, {Mikkel Aabech} and Kirsten Schauser",
year = "2007",
language = "English",
volume = "35",
pages = "s823--s830",
journal = "Acta Scientiae Veterinariae",
issn = "1678-0345",
publisher = "Universidade Federal do Rio Grande do Sul",
number = "Suppl. 3",

}

RIS

TY - JOUR

T1 - Embryonic stem cells in pig and cattle

T2 - derivation, culture and potential applications

AU - Maddox-Hyttel, Poul

AU - Wolf, Xenia Asbæk

AU - Rasmussen, Mikkel Aabech

AU - Schauser, Kirsten

PY - 2007

Y1 - 2007

N2 - Porcine and bovine cell lines derived from the inner cell mass (ICM) or epiblasts of blastocysts have been maintained over extended periods of time and characterized by morphology, identification of some stem cell markers and, in few cases, by production of chimaeric offspring. However, germ line transmission in chimaeras has never been obtained. Due to this incomplete characterization of the cell lines, the expression embryonic stem (ES)-like cells is presently used in pig and cattle. The ICM or epiblast can be isolated from the blastocyst by whole blastocyst culture, mechanical isolation, or immunosurgery, and they are generally cultured on feeder cells. The resulting ES-like cells may be differentiated in vivo by chimaera and teratoma formation or in vitro by embryoid body formation and monolayer induction. It is likely that more well characterized and stable porcine and bovine ES cell lines will be available over the coming years. However, in order to reach this goal further systematic research is needed. Such cell lines hold promises for developing adequate models for human ES cell therapy and they may open for new avenues for the production of genetically modified animals as the ES cells ahve indefinite selfrenewal capacity and may be more prone for homologous recombination. Finally, ES cell lines established from blastocysts, which are genetically modified to carry human disease genes, may be differentiated into particular cell populations that may allow for studies of disease mechanisms at the cellular level in vitro as a parallel to studies on whole animal models born from transfer of similar genetically modified embryos.

AB - Porcine and bovine cell lines derived from the inner cell mass (ICM) or epiblasts of blastocysts have been maintained over extended periods of time and characterized by morphology, identification of some stem cell markers and, in few cases, by production of chimaeric offspring. However, germ line transmission in chimaeras has never been obtained. Due to this incomplete characterization of the cell lines, the expression embryonic stem (ES)-like cells is presently used in pig and cattle. The ICM or epiblast can be isolated from the blastocyst by whole blastocyst culture, mechanical isolation, or immunosurgery, and they are generally cultured on feeder cells. The resulting ES-like cells may be differentiated in vivo by chimaera and teratoma formation or in vitro by embryoid body formation and monolayer induction. It is likely that more well characterized and stable porcine and bovine ES cell lines will be available over the coming years. However, in order to reach this goal further systematic research is needed. Such cell lines hold promises for developing adequate models for human ES cell therapy and they may open for new avenues for the production of genetically modified animals as the ES cells ahve indefinite selfrenewal capacity and may be more prone for homologous recombination. Finally, ES cell lines established from blastocysts, which are genetically modified to carry human disease genes, may be differentiated into particular cell populations that may allow for studies of disease mechanisms at the cellular level in vitro as a parallel to studies on whole animal models born from transfer of similar genetically modified embryos.

KW - Former LIFE faculty

KW - Embryonic stem cells

KW - pig

KW - cattle

KW - pluripotency

KW - differentiation

M3 - Journal article

VL - 35

SP - s823-s830

JO - Acta Scientiae Veterinariae

JF - Acta Scientiae Veterinariae

SN - 1678-0345

IS - Suppl. 3

ER -

ID: 8078423