Activation of the cannabinoid receptor type 2 by the agonist JWH133 promotes the first wave of in vitro spermatogenesis

Abstract

Background Oncological procedures have irreversible side effects on germ cells for childhood cancer survival boys. In vitro culture of prepubertal testicular tissue has been proposed to restore fertility; however, recent data on animal models showed that meiotic and post‐meiotic progression was impaired. Objectives As potential key inducers of the mitosis‐meiosis switch, type 2 cannabinoid receptor (CB2) has been proposed to play a central role in the meiotic entry of male germ cells. Herein, the in vitro first spermatogenesis wave in mice was used to understand the impact of CB2 activation on the differentiation of spermatogonia until elongated spermatids. Materials and methods A first set of cultured testicular explants of 6.5 days post‐partum (dpp) mice was performed to assess the impact of a range of JWH133 supplementation (10 nm, 100 nm, 1 µm, 10 µm). Then, the progressive development of germ cells at key timepoints of spermatogenesis was evaluated throughout (i) in vitro culture (day 2 [D2], D3, D6, D10, D18, and D30) coupled with (ii) in vivo counterparts (8.5, 9.5, 12.5, 16.5, 24.5, and 36.5 dpp). Results CB2 was detected at the plasma membrane of cells, and a successful completion of spermatogenesis was obtained in vitro. One day after the activation of CB2 by 1 μm of the agonist JWH133, percentage of zygotene spermatocyte I increased. Conclusion After 30 days of culture, (i) an enrichment of haploid germ cells detected by flow cytometry, (ii) a reduced necrotic area, and (iii) an increase in the density of post‐meiotic germ cells were observed. We showed that the activation of CB2 improves in vitro entry into meiosis and differentiation of spermatogonia, mimicking physiological meiotic transition.

The organotypic culture of mouse seminiferous tubules as a reliable methodology for the study of meiosisin vitro

“…Furthermore, more recent studies succeeded in producing functional sperm from primitive spermatogonia in explanted neonatal mouse testis tissues [21]. Since then, several researchers have used this methodology to display functional approaches to the study of mouse spermatogenesis [22][23][24][25][26][27][28][29].…”

“…Further studies succeeded in producing functional sperm from primitive spermatogonia in explanted neonatal mouse testis tissues [21]. Since then, several researchers have used this methodology to display functional approaches to the study of mouse spermatogenesis [22][23][24][25][26][27][28][29][30]. Latest advances using modified methodologies built upon the foundation of original protocols, have proposed that culturing isolated spermatogonia tubules, as opposed to tissue masses, offer distinct advantages in precisely evaluating the diverse environmental factors influencing the progression of spermatogenesis [31].…”