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Expression of genes involved in early cell fate decisions in human embryos and their regulation by growth factors

Expression of genes involved in early cell fate decisions in human embryos and their regulation by growth factors
Expression of genes involved in early cell fate decisions in human embryos and their regulation by growth factors
Little is understood about the regulation of gene expression in human preimplantation embryos. We set out to examine the expression in human preimplantation embryos of a number of genes known to be critical for early development of the murine embryo. The expression profile of these genes was analysed throughout preimplantation development and in response to growth factor (GF) stimulation. Developmental expression of a number of genes was similar to that seen in murine embryos (OCT3B/4, CDX2, NANOG). However, GATA6 is expressed throughout preimplantation development in the human. Embryos were cultured in IGF-I, leukaemia inhibitory factor (LIF) or heparin-binding EGF-like growth factor (HBEGF), all of which are known to stimulate the development of human embryos. Our data show that culture in HBEGF and LIF appears to facilitate human embryo expression of a number of genes: ERBB4 (LIF) and LIFR and DSC2 (HBEGF) while in the presence of HBEGF no blastocysts expressed EOMES and when cultured with LIF only two out of nine blastocysts expressed TBN. These data improve our knowledge of the similarities between human and murine embryos and the influence of GFs on human embryo gene expression. Results from this study will improve the understanding of cell fate decisions in early human embryos, which has important implications for both IVF treatment and the derivation of human embryonic stem cells.
cultured, leukemia inhibitory factor, morula, gene expression profiling, growth, drug effects, cleavage stage, intercellular signaling peptides and proteins, gene expression regulation, methods, embryonic development, peptides, immunohistochemistry, expression, stem cells, human, metabolism, blastocyst, embryo, embryonic stem cells, cells, cell differentiation, ovum, proteins, genetics, physiology, polymerase chain reaction, protein, leukemia, pharmacology, humans, insulin-like growth factor i, genes, research support, gene expression, developmental, treatment, culture, research, pregnancy, female, zygote, stem-cells
0022-4251
635-647
Kimber, S.J.
3c71cb00-e8c0-44d1-9595-99f748d71a3d
Sneddon, S.F.
b86273f2-c181-482a-a81b-78e61ace1a18
Bloor, D.J.
1533eaae-ff29-48a9-b1e8-682381c634f7
El-Bareg, A.M.
796346b5-44b0-4209-9f53-07832a927189
Hawkhead, J.A.
d1abbaa7-7436-4151-937f-5c0391f9834c
Metcalfe, A.D.
6d07cce3-c703-4876-a2d4-4f3bc2604445
Houghton, F.D.
53946041-127e-45a8-9edb-bf4b3c23005f
Leese, H.J.
1f369c23-4361-4534-a093-54699ec5eceb
Rutherford, A.
1271feba-25ce-4d78-836f-c4702064b8f6
Lieberman, B.A.
a1ca59f7-b008-4cad-ad0b-b9d13aef4bcf
Brison, D.R.
82c402a8-ad44-4afb-b8ec-04a70cc00914
Kimber, S.J.
3c71cb00-e8c0-44d1-9595-99f748d71a3d
Sneddon, S.F.
b86273f2-c181-482a-a81b-78e61ace1a18
Bloor, D.J.
1533eaae-ff29-48a9-b1e8-682381c634f7
El-Bareg, A.M.
796346b5-44b0-4209-9f53-07832a927189
Hawkhead, J.A.
d1abbaa7-7436-4151-937f-5c0391f9834c
Metcalfe, A.D.
6d07cce3-c703-4876-a2d4-4f3bc2604445
Houghton, F.D.
53946041-127e-45a8-9edb-bf4b3c23005f
Leese, H.J.
1f369c23-4361-4534-a093-54699ec5eceb
Rutherford, A.
1271feba-25ce-4d78-836f-c4702064b8f6
Lieberman, B.A.
a1ca59f7-b008-4cad-ad0b-b9d13aef4bcf
Brison, D.R.
82c402a8-ad44-4afb-b8ec-04a70cc00914

Kimber, S.J., Sneddon, S.F., Bloor, D.J., El-Bareg, A.M., Hawkhead, J.A., Metcalfe, A.D., Houghton, F.D., Leese, H.J., Rutherford, A., Lieberman, B.A. and Brison, D.R. (2008) Expression of genes involved in early cell fate decisions in human embryos and their regulation by growth factors. Reproduction, 135 (5), 635-647. (doi:10.1530/REP-07-0359).

Record type: Article

Abstract

Little is understood about the regulation of gene expression in human preimplantation embryos. We set out to examine the expression in human preimplantation embryos of a number of genes known to be critical for early development of the murine embryo. The expression profile of these genes was analysed throughout preimplantation development and in response to growth factor (GF) stimulation. Developmental expression of a number of genes was similar to that seen in murine embryos (OCT3B/4, CDX2, NANOG). However, GATA6 is expressed throughout preimplantation development in the human. Embryos were cultured in IGF-I, leukaemia inhibitory factor (LIF) or heparin-binding EGF-like growth factor (HBEGF), all of which are known to stimulate the development of human embryos. Our data show that culture in HBEGF and LIF appears to facilitate human embryo expression of a number of genes: ERBB4 (LIF) and LIFR and DSC2 (HBEGF) while in the presence of HBEGF no blastocysts expressed EOMES and when cultured with LIF only two out of nine blastocysts expressed TBN. These data improve our knowledge of the similarities between human and murine embryos and the influence of GFs on human embryo gene expression. Results from this study will improve the understanding of cell fate decisions in early human embryos, which has important implications for both IVF treatment and the derivation of human embryonic stem cells.

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More information

Published date: May 2008
Keywords: cultured, leukemia inhibitory factor, morula, gene expression profiling, growth, drug effects, cleavage stage, intercellular signaling peptides and proteins, gene expression regulation, methods, embryonic development, peptides, immunohistochemistry, expression, stem cells, human, metabolism, blastocyst, embryo, embryonic stem cells, cells, cell differentiation, ovum, proteins, genetics, physiology, polymerase chain reaction, protein, leukemia, pharmacology, humans, insulin-like growth factor i, genes, research support, gene expression, developmental, treatment, culture, research, pregnancy, female, zygote, stem-cells

Identifiers

Local EPrints ID: 59933
URI: http://eprints.soton.ac.uk/id/eprint/59933
ISSN: 0022-4251
PURE UUID: f6bc3c97-54ad-4f07-9169-61204cb8b859
ORCID for F.D. Houghton: ORCID iD orcid.org/0000-0002-5167-1694

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Date deposited: 17 Sep 2008
Last modified: 16 Mar 2024 03:49

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Contributors

Author: S.J. Kimber
Author: S.F. Sneddon
Author: D.J. Bloor
Author: A.M. El-Bareg
Author: J.A. Hawkhead
Author: A.D. Metcalfe
Author: F.D. Houghton ORCID iD
Author: H.J. Leese
Author: A. Rutherford
Author: B.A. Lieberman
Author: D.R. Brison

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