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Effects of Vitamin A on In Vitro Maturation of Pre-Pubertal Mouse Spermatogonial Stem Cells

Testicular tissue cryopreservation is the only potential option for fertility preservation in pre-pubertal boys exposed to gonadotoxic treatment. Completion of spermatogenesis after in vitro maturation is one of the future uses of harvested testicular tissue. The purpose of the current study was to...

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Autores principales: Travers, Albanne, Arkoun, Brahim, Safsaf, Athmane, Milazzo, Jean-Pierre, Absyte, Anne, Bironneau, Amandine, Perdrix, Anne, Sibert, Louis, Macé, Bertrand, Cauliez, Bruno, Rives, Nathalie
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3857286/
https://www.ncbi.nlm.nih.gov/pubmed/24349372
http://dx.doi.org/10.1371/journal.pone.0082819
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author Travers, Albanne
Arkoun, Brahim
Safsaf, Athmane
Milazzo, Jean-Pierre
Absyte, Anne
Bironneau, Amandine
Perdrix, Anne
Sibert, Louis
Macé, Bertrand
Cauliez, Bruno
Rives, Nathalie
author_facet Travers, Albanne
Arkoun, Brahim
Safsaf, Athmane
Milazzo, Jean-Pierre
Absyte, Anne
Bironneau, Amandine
Perdrix, Anne
Sibert, Louis
Macé, Bertrand
Cauliez, Bruno
Rives, Nathalie
author_sort Travers, Albanne
collection PubMed
description Testicular tissue cryopreservation is the only potential option for fertility preservation in pre-pubertal boys exposed to gonadotoxic treatment. Completion of spermatogenesis after in vitro maturation is one of the future uses of harvested testicular tissue. The purpose of the current study was to evaluate the effects of vitamin A on in vitro maturation of fresh and frozen-thawed mouse pre-pubertal spermatogonial stem cells in an organ culture system. Pre-pubertal CD1 mouse fresh testes were cultured for 7 (D7), 9 (D9) and 11 (D11) days using an organ culture system. Basal medium was supplemented with different concentrations of retinol (Re) or retinoic acid (RA) alone or in combination. Seminiferous tubule morphology (tubule diameter, intra-tubular cell type), intra-tubular cell death and proliferation (PCNA antibody) and testosterone level were assessed at D7, D9 and D11. Pre-pubertal mouse testicular tissue were frozen after a soaking temperature performed at -7°C, -8°C or -9°C and after thawing, were cultured for 9 days, using the culture medium preserving the best fresh tissue functionality. Retinoic acid at 10(-6)M and retinol at 3.3.10(-7)M, as well as retinol 10(-6)M are favourable for seminiferous tubule growth, maintenance of intra-tubular cell proliferation and germ cell differentiation of fresh pre-pubertal mouse spermatogonia. Structural and functional integrity of frozen-thawed testicular tissue appeared to be well-preserved after soaking temperature at -8°C, after 9 days of organotypic culture using 10(-6)M retinol. RA and Re can control in vitro germ cell proliferation and differentiation. Re at a concentration of 10(-6)M maintains intra-tubular cell proliferation and the ability of spermatogonia to initiate spermatogenesis in fresh and frozen pre-pubertal mouse testicular tissue using a soaking temperature at -8°C. Our data suggested a possible human application for in vitro maturation of cryopreserved pre-pubertal testicular tissue.
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spelling pubmed-38572862013-12-13 Effects of Vitamin A on In Vitro Maturation of Pre-Pubertal Mouse Spermatogonial Stem Cells Travers, Albanne Arkoun, Brahim Safsaf, Athmane Milazzo, Jean-Pierre Absyte, Anne Bironneau, Amandine Perdrix, Anne Sibert, Louis Macé, Bertrand Cauliez, Bruno Rives, Nathalie PLoS One Research Article Testicular tissue cryopreservation is the only potential option for fertility preservation in pre-pubertal boys exposed to gonadotoxic treatment. Completion of spermatogenesis after in vitro maturation is one of the future uses of harvested testicular tissue. The purpose of the current study was to evaluate the effects of vitamin A on in vitro maturation of fresh and frozen-thawed mouse pre-pubertal spermatogonial stem cells in an organ culture system. Pre-pubertal CD1 mouse fresh testes were cultured for 7 (D7), 9 (D9) and 11 (D11) days using an organ culture system. Basal medium was supplemented with different concentrations of retinol (Re) or retinoic acid (RA) alone or in combination. Seminiferous tubule morphology (tubule diameter, intra-tubular cell type), intra-tubular cell death and proliferation (PCNA antibody) and testosterone level were assessed at D7, D9 and D11. Pre-pubertal mouse testicular tissue were frozen after a soaking temperature performed at -7°C, -8°C or -9°C and after thawing, were cultured for 9 days, using the culture medium preserving the best fresh tissue functionality. Retinoic acid at 10(-6)M and retinol at 3.3.10(-7)M, as well as retinol 10(-6)M are favourable for seminiferous tubule growth, maintenance of intra-tubular cell proliferation and germ cell differentiation of fresh pre-pubertal mouse spermatogonia. Structural and functional integrity of frozen-thawed testicular tissue appeared to be well-preserved after soaking temperature at -8°C, after 9 days of organotypic culture using 10(-6)M retinol. RA and Re can control in vitro germ cell proliferation and differentiation. Re at a concentration of 10(-6)M maintains intra-tubular cell proliferation and the ability of spermatogonia to initiate spermatogenesis in fresh and frozen pre-pubertal mouse testicular tissue using a soaking temperature at -8°C. Our data suggested a possible human application for in vitro maturation of cryopreserved pre-pubertal testicular tissue. Public Library of Science 2013-12-09 /pmc/articles/PMC3857286/ /pubmed/24349372 http://dx.doi.org/10.1371/journal.pone.0082819 Text en © 2013 Travers et al http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Travers, Albanne
Arkoun, Brahim
Safsaf, Athmane
Milazzo, Jean-Pierre
Absyte, Anne
Bironneau, Amandine
Perdrix, Anne
Sibert, Louis
Macé, Bertrand
Cauliez, Bruno
Rives, Nathalie
Effects of Vitamin A on In Vitro Maturation of Pre-Pubertal Mouse Spermatogonial Stem Cells
title Effects of Vitamin A on In Vitro Maturation of Pre-Pubertal Mouse Spermatogonial Stem Cells
title_full Effects of Vitamin A on In Vitro Maturation of Pre-Pubertal Mouse Spermatogonial Stem Cells
title_fullStr Effects of Vitamin A on In Vitro Maturation of Pre-Pubertal Mouse Spermatogonial Stem Cells
title_full_unstemmed Effects of Vitamin A on In Vitro Maturation of Pre-Pubertal Mouse Spermatogonial Stem Cells
title_short Effects of Vitamin A on In Vitro Maturation of Pre-Pubertal Mouse Spermatogonial Stem Cells
title_sort effects of vitamin a on in vitro maturation of pre-pubertal mouse spermatogonial stem cells
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3857286/
https://www.ncbi.nlm.nih.gov/pubmed/24349372
http://dx.doi.org/10.1371/journal.pone.0082819
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