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CD14 is a unique membrane marker of porcine spermatogonial stem cells, regulating their differentiation
Molecular markers of spermatogonia are necessary for studies on spermatogonial stem cells (SSCs) and improving our understanding of molecular and cellular biology of spermatogenesis. Although studies of germ cell surface marker have been extensively conducted in the testes of rodents, these markers...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6620343/ https://www.ncbi.nlm.nih.gov/pubmed/31292454 http://dx.doi.org/10.1038/s41598-019-46000-6 |
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author | Park, Hyun-Jung Lee, Won-Young Park, Chankyu Hong, Kwonho Song, Hyuk |
author_facet | Park, Hyun-Jung Lee, Won-Young Park, Chankyu Hong, Kwonho Song, Hyuk |
author_sort | Park, Hyun-Jung |
collection | PubMed |
description | Molecular markers of spermatogonia are necessary for studies on spermatogonial stem cells (SSCs) and improving our understanding of molecular and cellular biology of spermatogenesis. Although studies of germ cell surface marker have been extensively conducted in the testes of rodents, these markers have not been well studied in domestic animals. We aimed to determine the expression pattern of cluster of differentiation 14 (CD14) in developing porcine testes and cultured porcine SSCs (pSSCs), as well as its role in pSSC colony formation. Interestingly, expression of CD14 was observed in porcine testes with PGP9.5-positive undifferentiated spermatogonia at all developmental stages. In addition, in vitro cultured pSSCs expressed CD14 and showed successful colony formation, as determined by fluorescence-activated cell sorting and flow cytometry. PKH26 dye-stained CD14-positive cells transplants were performed into the testes of recipient mice, which were depleted of both testicular germ and somatic cells from immunodeficiency mice and were shown to colonise the recipient testes. Moreover, a colony-forming assay showed that the development of pSSC colonies was disrupted by a high concentration of lipopolysaccharide. These studies indicated that CD14 is surface marker of early spermatogonia in developing porcine testes and in pSSCs, suggesting a role for CD14 in porcine spermatogenesis. |
format | Online Article Text |
id | pubmed-6620343 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-66203432019-07-18 CD14 is a unique membrane marker of porcine spermatogonial stem cells, regulating their differentiation Park, Hyun-Jung Lee, Won-Young Park, Chankyu Hong, Kwonho Song, Hyuk Sci Rep Article Molecular markers of spermatogonia are necessary for studies on spermatogonial stem cells (SSCs) and improving our understanding of molecular and cellular biology of spermatogenesis. Although studies of germ cell surface marker have been extensively conducted in the testes of rodents, these markers have not been well studied in domestic animals. We aimed to determine the expression pattern of cluster of differentiation 14 (CD14) in developing porcine testes and cultured porcine SSCs (pSSCs), as well as its role in pSSC colony formation. Interestingly, expression of CD14 was observed in porcine testes with PGP9.5-positive undifferentiated spermatogonia at all developmental stages. In addition, in vitro cultured pSSCs expressed CD14 and showed successful colony formation, as determined by fluorescence-activated cell sorting and flow cytometry. PKH26 dye-stained CD14-positive cells transplants were performed into the testes of recipient mice, which were depleted of both testicular germ and somatic cells from immunodeficiency mice and were shown to colonise the recipient testes. Moreover, a colony-forming assay showed that the development of pSSC colonies was disrupted by a high concentration of lipopolysaccharide. These studies indicated that CD14 is surface marker of early spermatogonia in developing porcine testes and in pSSCs, suggesting a role for CD14 in porcine spermatogenesis. Nature Publishing Group UK 2019-07-10 /pmc/articles/PMC6620343/ /pubmed/31292454 http://dx.doi.org/10.1038/s41598-019-46000-6 Text en © The Author(s) 2019 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Park, Hyun-Jung Lee, Won-Young Park, Chankyu Hong, Kwonho Song, Hyuk CD14 is a unique membrane marker of porcine spermatogonial stem cells, regulating their differentiation |
title | CD14 is a unique membrane marker of porcine spermatogonial stem cells, regulating their differentiation |
title_full | CD14 is a unique membrane marker of porcine spermatogonial stem cells, regulating their differentiation |
title_fullStr | CD14 is a unique membrane marker of porcine spermatogonial stem cells, regulating their differentiation |
title_full_unstemmed | CD14 is a unique membrane marker of porcine spermatogonial stem cells, regulating their differentiation |
title_short | CD14 is a unique membrane marker of porcine spermatogonial stem cells, regulating their differentiation |
title_sort | cd14 is a unique membrane marker of porcine spermatogonial stem cells, regulating their differentiation |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6620343/ https://www.ncbi.nlm.nih.gov/pubmed/31292454 http://dx.doi.org/10.1038/s41598-019-46000-6 |
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