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Germline competent mesoderm: the substrate for vertebrate germline and somatic stem cells?

In vitro production of tissue-specific stem cells [e.g. haematopoietic stem cells (HSCs)] is a key goal of regenerative medicine. However, recent efforts to produce fully functional tissue-specific stem cells have fallen short. One possible cause of shortcomings may be that model organisms used to c...

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Autores principales: Savage, Aaron M., Alberio, Ramiro, Johnson, Andrew D.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Company of Biologists Ltd 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8524722/
https://www.ncbi.nlm.nih.gov/pubmed/34648017
http://dx.doi.org/10.1242/bio.058890
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author Savage, Aaron M.
Alberio, Ramiro
Johnson, Andrew D.
author_facet Savage, Aaron M.
Alberio, Ramiro
Johnson, Andrew D.
author_sort Savage, Aaron M.
collection PubMed
description In vitro production of tissue-specific stem cells [e.g. haematopoietic stem cells (HSCs)] is a key goal of regenerative medicine. However, recent efforts to produce fully functional tissue-specific stem cells have fallen short. One possible cause of shortcomings may be that model organisms used to characterize basic vertebrate embryology (Xenopus, zebrafish, chick) may employ molecular mechanisms for stem cell specification that are not conserved in humans, a prominent example being the specification of primordial germ cells (PGCs). Germ plasm irreversibly specifies PGCs in many models; however, it is not conserved in humans, which produce PGCs from tissue termed germline-competent mesoderm (GLCM). GLCM is not conserved in organisms containing germ plasm, or even in mice, but understanding its developmental potential could unlock successful production of other stem cell types. GLCM was first discovered in embryos from the axolotl and its conservation has since been demonstrated in pigs, which develop from a flat-disc embryo like humans. Together these findings suggest that GLCM is a conserved basal trait of vertebrate embryos. Moreover, the immortal nature of germ cells suggests that immortality is retained during GLCM specification; here we suggest that the demonstrated pluripotency of GLCM accounts for retention of immortality in somatic stem cell types as well. This article has an associated Future Leaders to Watch interview with the author of the paper.
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spelling pubmed-85247222021-10-19 Germline competent mesoderm: the substrate for vertebrate germline and somatic stem cells? Savage, Aaron M. Alberio, Ramiro Johnson, Andrew D. Biol Open Review In vitro production of tissue-specific stem cells [e.g. haematopoietic stem cells (HSCs)] is a key goal of regenerative medicine. However, recent efforts to produce fully functional tissue-specific stem cells have fallen short. One possible cause of shortcomings may be that model organisms used to characterize basic vertebrate embryology (Xenopus, zebrafish, chick) may employ molecular mechanisms for stem cell specification that are not conserved in humans, a prominent example being the specification of primordial germ cells (PGCs). Germ plasm irreversibly specifies PGCs in many models; however, it is not conserved in humans, which produce PGCs from tissue termed germline-competent mesoderm (GLCM). GLCM is not conserved in organisms containing germ plasm, or even in mice, but understanding its developmental potential could unlock successful production of other stem cell types. GLCM was first discovered in embryos from the axolotl and its conservation has since been demonstrated in pigs, which develop from a flat-disc embryo like humans. Together these findings suggest that GLCM is a conserved basal trait of vertebrate embryos. Moreover, the immortal nature of germ cells suggests that immortality is retained during GLCM specification; here we suggest that the demonstrated pluripotency of GLCM accounts for retention of immortality in somatic stem cell types as well. This article has an associated Future Leaders to Watch interview with the author of the paper. The Company of Biologists Ltd 2021-10-14 /pmc/articles/PMC8524722/ /pubmed/34648017 http://dx.doi.org/10.1242/bio.058890 Text en © 2021. Published by The Company of Biologists Ltd https://creativecommons.org/licenses/by/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution and reproduction in any medium provided that the original work is properly attributed.
spellingShingle Review
Savage, Aaron M.
Alberio, Ramiro
Johnson, Andrew D.
Germline competent mesoderm: the substrate for vertebrate germline and somatic stem cells?
title Germline competent mesoderm: the substrate for vertebrate germline and somatic stem cells?
title_full Germline competent mesoderm: the substrate for vertebrate germline and somatic stem cells?
title_fullStr Germline competent mesoderm: the substrate for vertebrate germline and somatic stem cells?
title_full_unstemmed Germline competent mesoderm: the substrate for vertebrate germline and somatic stem cells?
title_short Germline competent mesoderm: the substrate for vertebrate germline and somatic stem cells?
title_sort germline competent mesoderm: the substrate for vertebrate germline and somatic stem cells?
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8524722/
https://www.ncbi.nlm.nih.gov/pubmed/34648017
http://dx.doi.org/10.1242/bio.058890
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