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Sex-Specific Isolation and Propagation of Human Premeiotic Fetal Germ Cells and Germ Cell-Like Cells

The second trimester of human development is marked by asynchronous gonadal development hampering the isolation of homogenous populations of early and late fetal germ cells (FGCs). We evaluated the feasibility of using surface markers TNAP, PDPN, EPCAM and ITGA6 to isolate FGCs as well as human prim...

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Autores principales: Mishra, Swati, Taelman, Jasin, Chang, Yolanda W., Boel, Annekatrien, De Sutter, Petra, Heindryckx, Björn, Chuva De Sousa Lopes, Susana M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8156680/
https://www.ncbi.nlm.nih.gov/pubmed/34065661
http://dx.doi.org/10.3390/cells10051214
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author Mishra, Swati
Taelman, Jasin
Chang, Yolanda W.
Boel, Annekatrien
De Sutter, Petra
Heindryckx, Björn
Chuva De Sousa Lopes, Susana M.
author_facet Mishra, Swati
Taelman, Jasin
Chang, Yolanda W.
Boel, Annekatrien
De Sutter, Petra
Heindryckx, Björn
Chuva De Sousa Lopes, Susana M.
author_sort Mishra, Swati
collection PubMed
description The second trimester of human development is marked by asynchronous gonadal development hampering the isolation of homogenous populations of early and late fetal germ cells (FGCs). We evaluated the feasibility of using surface markers TNAP, PDPN, EPCAM and ITGA6 to isolate FGCs as well as human primordial germ cell-like cells (hPGCLCs) derived from embryonic stem cells (hESCs) from both sexes by fluorescence-activated cell sorting (FACS). Our results suggest that a combination of TNAP and PDPN was sufficient to separate populations of premeiotic FGCs and hPGCLCs in both sexes. This combination of antibodies also proved efficient in separating ‘mitotic’ from ‘retinoic-acid responsive’ female FGCs. Furthermore, we report that the differentiation efficiency of TNAP+PDPN+ hPGCLCs from hESCs was sex-independent, but the ability to propagate differed considerably between the sexes. In contrast to male, female hPGCLCs retained their characteristics and exhibited robust colony-forming ability when cultured for five days in medium containing LIF, forskolin and FGF2. We conclude that marked sex differences exist in the isolation and propagation of human FGCs and hPGCLCs. Our study provides novel insights relevant for the optimization of in vitro gametogenesis in humans.
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spelling pubmed-81566802021-05-28 Sex-Specific Isolation and Propagation of Human Premeiotic Fetal Germ Cells and Germ Cell-Like Cells Mishra, Swati Taelman, Jasin Chang, Yolanda W. Boel, Annekatrien De Sutter, Petra Heindryckx, Björn Chuva De Sousa Lopes, Susana M. Cells Article The second trimester of human development is marked by asynchronous gonadal development hampering the isolation of homogenous populations of early and late fetal germ cells (FGCs). We evaluated the feasibility of using surface markers TNAP, PDPN, EPCAM and ITGA6 to isolate FGCs as well as human primordial germ cell-like cells (hPGCLCs) derived from embryonic stem cells (hESCs) from both sexes by fluorescence-activated cell sorting (FACS). Our results suggest that a combination of TNAP and PDPN was sufficient to separate populations of premeiotic FGCs and hPGCLCs in both sexes. This combination of antibodies also proved efficient in separating ‘mitotic’ from ‘retinoic-acid responsive’ female FGCs. Furthermore, we report that the differentiation efficiency of TNAP+PDPN+ hPGCLCs from hESCs was sex-independent, but the ability to propagate differed considerably between the sexes. In contrast to male, female hPGCLCs retained their characteristics and exhibited robust colony-forming ability when cultured for five days in medium containing LIF, forskolin and FGF2. We conclude that marked sex differences exist in the isolation and propagation of human FGCs and hPGCLCs. Our study provides novel insights relevant for the optimization of in vitro gametogenesis in humans. MDPI 2021-05-16 /pmc/articles/PMC8156680/ /pubmed/34065661 http://dx.doi.org/10.3390/cells10051214 Text en © 2021 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Mishra, Swati
Taelman, Jasin
Chang, Yolanda W.
Boel, Annekatrien
De Sutter, Petra
Heindryckx, Björn
Chuva De Sousa Lopes, Susana M.
Sex-Specific Isolation and Propagation of Human Premeiotic Fetal Germ Cells and Germ Cell-Like Cells
title Sex-Specific Isolation and Propagation of Human Premeiotic Fetal Germ Cells and Germ Cell-Like Cells
title_full Sex-Specific Isolation and Propagation of Human Premeiotic Fetal Germ Cells and Germ Cell-Like Cells
title_fullStr Sex-Specific Isolation and Propagation of Human Premeiotic Fetal Germ Cells and Germ Cell-Like Cells
title_full_unstemmed Sex-Specific Isolation and Propagation of Human Premeiotic Fetal Germ Cells and Germ Cell-Like Cells
title_short Sex-Specific Isolation and Propagation of Human Premeiotic Fetal Germ Cells and Germ Cell-Like Cells
title_sort sex-specific isolation and propagation of human premeiotic fetal germ cells and germ cell-like cells
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8156680/
https://www.ncbi.nlm.nih.gov/pubmed/34065661
http://dx.doi.org/10.3390/cells10051214
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