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Vitrified canine testicular cells allow the formation of spermatogonial stem cells and seminiferous tubules following their xenotransplantation into nude mice

Belgian Malinois (BM), one of the excellent military dog breeds in South Korea, is usually castrated before sexual maturation. Therefore, the transfer of their genetic features to the next generation is difficult. To overcome this, testicular cells from 4-month-old BMs were frozen. Testicular cells...

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Autores principales: Lee, Kyung Hoon, Lee, Won Young, Kim, Dong Hoon, Lee, Seung Hoon, Do, Jung Tae, Park, Chankyu, Kim, Jae Hwan, Choi, Young Suk, Song, Hyuk
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4764824/
https://www.ncbi.nlm.nih.gov/pubmed/26907750
http://dx.doi.org/10.1038/srep21919
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author Lee, Kyung Hoon
Lee, Won Young
Kim, Dong Hoon
Lee, Seung Hoon
Do, Jung Tae
Park, Chankyu
Kim, Jae Hwan
Choi, Young Suk
Song, Hyuk
author_facet Lee, Kyung Hoon
Lee, Won Young
Kim, Dong Hoon
Lee, Seung Hoon
Do, Jung Tae
Park, Chankyu
Kim, Jae Hwan
Choi, Young Suk
Song, Hyuk
author_sort Lee, Kyung Hoon
collection PubMed
description Belgian Malinois (BM), one of the excellent military dog breeds in South Korea, is usually castrated before sexual maturation. Therefore, the transfer of their genetic features to the next generation is difficult. To overcome this, testicular cells from 4-month-old BMs were frozen. Testicular cells were thawed after 3 months and cultured in StemPro-34 medium. Spermatogonial stem cell (SSC) characteristics were determined by the transplantation of the cultured germ cell-derived colonies (GDCs) into empty testes, containing only several endogenous SSCs and Sertoli cells, of immunodeficient mice, 4 weeks after busulfan treatment. Following the implantation, the transplanted cells localized in the basement membrane of the seminiferous tubules, and ultimately colonized the recipient testes. Xenotransplantation of GDCs together with testicular somatic cells conjugated with extracellular matrix (ECM), led to the formation of de novo seminiferous tubules. These seminiferous tubules were mostly composed of Sertoli cells. Some germ cells were localized in the basement membrane of seminiferous tubules. This study revealed that BM-derived SSCs, obtained from the castrated testes, might be a valuable tool for the transfer of BM genetic features to the next generation.
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spelling pubmed-47648242016-03-02 Vitrified canine testicular cells allow the formation of spermatogonial stem cells and seminiferous tubules following their xenotransplantation into nude mice Lee, Kyung Hoon Lee, Won Young Kim, Dong Hoon Lee, Seung Hoon Do, Jung Tae Park, Chankyu Kim, Jae Hwan Choi, Young Suk Song, Hyuk Sci Rep Article Belgian Malinois (BM), one of the excellent military dog breeds in South Korea, is usually castrated before sexual maturation. Therefore, the transfer of their genetic features to the next generation is difficult. To overcome this, testicular cells from 4-month-old BMs were frozen. Testicular cells were thawed after 3 months and cultured in StemPro-34 medium. Spermatogonial stem cell (SSC) characteristics were determined by the transplantation of the cultured germ cell-derived colonies (GDCs) into empty testes, containing only several endogenous SSCs and Sertoli cells, of immunodeficient mice, 4 weeks after busulfan treatment. Following the implantation, the transplanted cells localized in the basement membrane of the seminiferous tubules, and ultimately colonized the recipient testes. Xenotransplantation of GDCs together with testicular somatic cells conjugated with extracellular matrix (ECM), led to the formation of de novo seminiferous tubules. These seminiferous tubules were mostly composed of Sertoli cells. Some germ cells were localized in the basement membrane of seminiferous tubules. This study revealed that BM-derived SSCs, obtained from the castrated testes, might be a valuable tool for the transfer of BM genetic features to the next generation. Nature Publishing Group 2016-02-24 /pmc/articles/PMC4764824/ /pubmed/26907750 http://dx.doi.org/10.1038/srep21919 Text en Copyright © 2016, Macmillan Publishers Limited http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/
spellingShingle Article
Lee, Kyung Hoon
Lee, Won Young
Kim, Dong Hoon
Lee, Seung Hoon
Do, Jung Tae
Park, Chankyu
Kim, Jae Hwan
Choi, Young Suk
Song, Hyuk
Vitrified canine testicular cells allow the formation of spermatogonial stem cells and seminiferous tubules following their xenotransplantation into nude mice
title Vitrified canine testicular cells allow the formation of spermatogonial stem cells and seminiferous tubules following their xenotransplantation into nude mice
title_full Vitrified canine testicular cells allow the formation of spermatogonial stem cells and seminiferous tubules following their xenotransplantation into nude mice
title_fullStr Vitrified canine testicular cells allow the formation of spermatogonial stem cells and seminiferous tubules following their xenotransplantation into nude mice
title_full_unstemmed Vitrified canine testicular cells allow the formation of spermatogonial stem cells and seminiferous tubules following their xenotransplantation into nude mice
title_short Vitrified canine testicular cells allow the formation of spermatogonial stem cells and seminiferous tubules following their xenotransplantation into nude mice
title_sort vitrified canine testicular cells allow the formation of spermatogonial stem cells and seminiferous tubules following their xenotransplantation into nude mice
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4764824/
https://www.ncbi.nlm.nih.gov/pubmed/26907750
http://dx.doi.org/10.1038/srep21919
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