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Haploid Germ Cells Generated in Organotypic Culture of Testicular Tissue From Prepubertal Boys

Authors :
UCL - SSS/IREC/GYNE - Pôle de Gynécologie
UCL - SSS/IREC/CTMA - Centre de technologies moléculaires appliquées (plate-forme technologique)
UCL - SSS/IREC/MORF - Pôle de Morphologie
UCL - (SLuc) Service de biochimie médicale
UCL - (SLuc) Service d'anatomie pathologique
UCL - (SLuc) Service de gynécologie et d'andrologie
De Michele, Francesca
Poels, Jonathan
Vermeulen, Maxime
Ambroise, Jérôme
Gruson, Damien
Guiot, Yves
Wyns, Christine
UCL - SSS/IREC/GYNE - Pôle de Gynécologie
UCL - SSS/IREC/CTMA - Centre de technologies moléculaires appliquées (plate-forme technologique)
UCL - SSS/IREC/MORF - Pôle de Morphologie
UCL - (SLuc) Service de biochimie médicale
UCL - (SLuc) Service d'anatomie pathologique
UCL - (SLuc) Service de gynécologie et d'andrologie
De Michele, Francesca
Poels, Jonathan
Vermeulen, Maxime
Ambroise, Jérôme
Gruson, Damien
Guiot, Yves
Wyns, Christine
Source :
Frontiers in Physiology, Vol. 9, p. 1413 [1-18] (2018)
Publication Year :
2018

Abstract

While in mice various studies have described the completion of spermatogenesis in vitro using either organotypic culture of prepubertal testicular tissue or 3D culture of isolated cells, in humans it has not been possible to achieve germ cell differentiation from immature testicular tissue (ITT). In our study, we evaluated the ability of human ITT to differentiate via a long-term organotypic culture of frozen–thawed 1 mm3 testicular fragments from five prepubertal boys in two different culture media. Tissue and supernatants were analyzed at regular intervals up to day 139. Sertoli cell (SC) viability and maturation was evaluated using immunohistochemistry (IHC) for SOX9, GDNF, anti-Mullerian hormone (AMH) and androgen receptor (AR), and AMH concentration in supernatants. Spermatogonia (SG) and proliferating cells were identified by MAGE-A4 (for SG) and Ki67 (for proliferating cells) via immunohistochemistry (IHC). Apoptotic cells were studied by active caspase 3. To evaluate Leydig cell (LC) functionality testosterone was measured in the supernatants and steroidogenic acute regulatory protein (STAR) IHC was performed. Germ cell differentiation was evaluated on Hematoxylin-Eosin histological sections, via IHC for synaptonemal complex 3 (SYCP3) for spermatocytes, Protein boule-like (BOLL) for spermatocytes and round spermatids, angiotensin-converting enzyme (ACE), protamine 2 and transition protein 1 (for elongated spermatids) and via chromogenic in situ hybridization (CISH). We reported the generation of meiotic and postmeiotic cells after 16 days of culture, as shown by the histological analyses, the presence of differentiation markers and the increase of haploid germ cells. We showed SC viability and maturation by a decrease of AMH secretion in the supernatants (p ≤ 0.001) while the number of SOX9 positive cells did not show any variation. A decrease of spermatogonia (p ≤ 0.001) was observed. The number of apoptotic cells did not vary. LC functionality was shown by

Details

Database :
OAIster
Journal :
Frontiers in Physiology, Vol. 9, p. 1413 [1-18] (2018)
Notes :
English
Publication Type :
Electronic Resource
Accession number :
edsoai.on1130449558
Document Type :
Electronic Resource