Cargando…
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...
Autores principales: | , , , , , , |
---|---|
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 |
_version_ | 1783699503169142784 |
---|---|
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. |
format | Online Article Text |
id | pubmed-8156680 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
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 |
work_keys_str_mv | AT mishraswati sexspecificisolationandpropagationofhumanpremeioticfetalgermcellsandgermcelllikecells AT taelmanjasin sexspecificisolationandpropagationofhumanpremeioticfetalgermcellsandgermcelllikecells AT changyolandaw sexspecificisolationandpropagationofhumanpremeioticfetalgermcellsandgermcelllikecells AT boelannekatrien sexspecificisolationandpropagationofhumanpremeioticfetalgermcellsandgermcelllikecells AT desutterpetra sexspecificisolationandpropagationofhumanpremeioticfetalgermcellsandgermcelllikecells AT heindryckxbjorn sexspecificisolationandpropagationofhumanpremeioticfetalgermcellsandgermcelllikecells AT chuvadesousalopessusanam sexspecificisolationandpropagationofhumanpremeioticfetalgermcellsandgermcelllikecells |