The Non-hormonal Male Contraceptive Adjudin Exerts its Effects via MAPs and Signaling Proteins mTORC1/rpS6 and FAK-Y407
Autor: | Chris K C Wong, Siwen Wu, C. Yan Cheng, Ren-Shan Ge, Bruno Silvestrini, Huitao Li, Fei Sun, Ming Yan, Lingling Wang |
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Rok vydání: | 2020 |
Předmět: |
Male
0301 basic medicine medicine.medical_specialty Indazoles Population Mechanistic Target of Rapamycin Complex 1 Biology Rats Sprague-Dawley Adherens junction 03 medical and health sciences 0302 clinical medicine Endocrinology Cadmium Chloride Internal medicine medicine Animals education Research Articles Ribosomal Protein S6 education.field_of_study Basal ectoplasmic specialization Apical ectoplasmic specialization Sertoli cell Rats Cell biology Hydrazines 030104 developmental biology medicine.anatomical_structure Gene Expression Regulation Focal Adhesion Kinase 1 Adjudin Microtubule-Associated Proteins Spermatogenesis 030217 neurology & neurosurgery Germ cell Signal Transduction |
Zdroj: | Endocrinology |
ISSN: | 1945-7170 0013-7227 |
DOI: | 10.1210/endocr/bqaa196 |
Popis: | Adjudin, 1-(2,4-dichlorobenzyl)-1H-indazole-3-carbohydrazide (formerly called AF-2364), is a nonhormonal male contraceptive, since it effectively induces reversible male infertility without perturbing the serum concentrations of follicle stimulating hormone (FSH), testosterone, and inhibin B based on studies in rats and rabbits. Adjudin was shown to exert its effects preferentially by perturbing the testis-specific actin-rich adherens junction (AJ) at the Sertoli–spermatid interface known as apical ectoplasmic specialization (apical ES), thereby effectively inducing spermatid exfoliation. Adjudin did not perturb germ cell development nor germ cell function. Also, it had no effects on Sertoli cell–cell AJ called basal ectoplasmic specialization (basal ES), which, together with tight junction constitute the blood-testis barrier (BTB), unless an acute dose of adjudin was used. Adjudin also did not perturb the population of spermatogonial stem cells nor Sertoli cells in the testis. However, the downstream signaling protein(s) utilized by adjudin to induce transient male infertility remains unexplored. Herein, using adult rats treated with adjudin and monitored changes in the phenotypes across the seminiferous epithelium between 6 and 96 h in parallel with the steady-state protein levels of an array of signaling and cytoskeletal regulatory proteins, recently shown to be involved in apical ES, basal ES and BTB function. It was shown that adjudin exerts its contraceptive effects through changes in microtubule associated proteins (MAPs) and signaling proteins mTORC1/rpS6 and p-FAK-Y407. These findings are important to not only study adjudin-mediated male infertility but also the biology of spermatogenesis. |
Databáze: | OpenAIRE |
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