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FGF, Insulin, and SMAD Signaling Cooperate for Avian Primordial Germ Cell Self-Renewal

Precise self-renewal of the germ cell lineage is fundamental to fertility and reproductive success. The early precursors for the germ lineage, primordial germ cells (PGCs), survive and proliferate in several embryonic locations during their migration to the embryonic gonad. By elucidating the active...

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Autores principales: Whyte, Jemima, Glover, James D., Woodcock, Mark, Brzeszczynska, Joanna, Taylor, Lorna, Sherman, Adrian, Kaiser, Pete, McGrew, Michael J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4682126/
https://www.ncbi.nlm.nih.gov/pubmed/26677769
http://dx.doi.org/10.1016/j.stemcr.2015.10.008
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author Whyte, Jemima
Glover, James D.
Woodcock, Mark
Brzeszczynska, Joanna
Taylor, Lorna
Sherman, Adrian
Kaiser, Pete
McGrew, Michael J.
author_facet Whyte, Jemima
Glover, James D.
Woodcock, Mark
Brzeszczynska, Joanna
Taylor, Lorna
Sherman, Adrian
Kaiser, Pete
McGrew, Michael J.
author_sort Whyte, Jemima
collection PubMed
description Precise self-renewal of the germ cell lineage is fundamental to fertility and reproductive success. The early precursors for the germ lineage, primordial germ cells (PGCs), survive and proliferate in several embryonic locations during their migration to the embryonic gonad. By elucidating the active signaling pathways in migratory PGCs in vivo, we were able to create culture conditions that recapitulate this embryonic germ cell environment. In defined medium conditions without feeder cells, the growth factors FGF2, insulin, and Activin A, signaling through their cognate-signaling pathways, were sufficient for self-renewal of germline-competent PGCs. Forced expression of constitutively active MEK1, AKT, and SMAD3 proteins could replace their respective upstream growth factors. Unexpectedly, we found that BMP4 could replace Activin A in non-clonal growth conditions. These defined medium conditions identify the key molecular pathways required for PGC self-renewal and will facilitate efforts in biobanking of chicken genetic resources and genome editing.
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spelling pubmed-46821262016-01-12 FGF, Insulin, and SMAD Signaling Cooperate for Avian Primordial Germ Cell Self-Renewal Whyte, Jemima Glover, James D. Woodcock, Mark Brzeszczynska, Joanna Taylor, Lorna Sherman, Adrian Kaiser, Pete McGrew, Michael J. Stem Cell Reports Article Precise self-renewal of the germ cell lineage is fundamental to fertility and reproductive success. The early precursors for the germ lineage, primordial germ cells (PGCs), survive and proliferate in several embryonic locations during their migration to the embryonic gonad. By elucidating the active signaling pathways in migratory PGCs in vivo, we were able to create culture conditions that recapitulate this embryonic germ cell environment. In defined medium conditions without feeder cells, the growth factors FGF2, insulin, and Activin A, signaling through their cognate-signaling pathways, were sufficient for self-renewal of germline-competent PGCs. Forced expression of constitutively active MEK1, AKT, and SMAD3 proteins could replace their respective upstream growth factors. Unexpectedly, we found that BMP4 could replace Activin A in non-clonal growth conditions. These defined medium conditions identify the key molecular pathways required for PGC self-renewal and will facilitate efforts in biobanking of chicken genetic resources and genome editing. Elsevier 2015-11-19 /pmc/articles/PMC4682126/ /pubmed/26677769 http://dx.doi.org/10.1016/j.stemcr.2015.10.008 Text en © 2015 The Authors http://creativecommons.org/licenses/by/4.0/ This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Whyte, Jemima
Glover, James D.
Woodcock, Mark
Brzeszczynska, Joanna
Taylor, Lorna
Sherman, Adrian
Kaiser, Pete
McGrew, Michael J.
FGF, Insulin, and SMAD Signaling Cooperate for Avian Primordial Germ Cell Self-Renewal
title FGF, Insulin, and SMAD Signaling Cooperate for Avian Primordial Germ Cell Self-Renewal
title_full FGF, Insulin, and SMAD Signaling Cooperate for Avian Primordial Germ Cell Self-Renewal
title_fullStr FGF, Insulin, and SMAD Signaling Cooperate for Avian Primordial Germ Cell Self-Renewal
title_full_unstemmed FGF, Insulin, and SMAD Signaling Cooperate for Avian Primordial Germ Cell Self-Renewal
title_short FGF, Insulin, and SMAD Signaling Cooperate for Avian Primordial Germ Cell Self-Renewal
title_sort fgf, insulin, and smad signaling cooperate for avian primordial germ cell self-renewal
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4682126/
https://www.ncbi.nlm.nih.gov/pubmed/26677769
http://dx.doi.org/10.1016/j.stemcr.2015.10.008
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