Postnatal developmental expression of apelin receptor proteins and its role in juvenile mice testis

• Published in: The Journal of steroid biochemistry and molecular biology 2022-11, Vol.224, p.106178, Article 106178
• Main Authors: Das, Milirani, Gurusubramanian, Guruswami, Roy, Vikas Kumar
• Format: Article
• Language: English
• Subjects: Androstenedione - blood; Animals; Apelin; Apelin - blood; Apelin - metabolism; Apelin Receptors - metabolism; Carrier Proteins; Estrogens; Male; Mice; ML221; Postnatal; Proliferation; Receptors, G-Protein-Coupled - genetics; Receptors, G-Protein-Coupled - metabolism; Sexual Development - drug effects; Sexual Development - genetics; Spermatogenesis - drug effects; Spermatogenesis - genetics; Testis; Testis - drug effects; Testis - metabolism; Testosterone; Testosterone - blood; Testosterone - metabolism
• ISSN: 0960-0760; 1879-1220; 1879-1220
• DOI: 10.1016/j.jsbmb.2022.106178

The expression of apelin system has been shown in the adult testis of rat and mice. It has also been emphasized that regulation of testicular activity in early stages is important to sustain normal testicular activity in adulthood. Since the expression of apelin receptor (APJ) has been shown in the adult testis, moreover, developmental expression of APJ and its role has not been explored yet. Thus, we have examined the testicular expression of APJ during postnatal stages with special reference to proliferation, apoptosis and hormone secretion in early postnatal stage. Postnatal analysis showed that circulating apelin was lowest at PND1 and maximum at PND42. Among testosterone, estrogen and androstenedione, only circulating testosterone showed a gradual increase from PND1 to PND42. Testicular expression of APJ was also developmenatly regulated from PND1 to PND42, revealing a positive correlation with circulating apelin, testosterone, and androstenedione. Immunohistochemical study showed that APJ was mainly confined to Leydig cells of early postnatal stages, whereas, seminiferous tubules at PND42 showed immunostaining in the round spermatids. APJ inhibition from PND14-PND20 by ML221 suppressed the testicular proliferation, increased apoptosis and increased estrogen secretion. However, expression of AR was down-regulated by ML221 treatment. Furthermore, ML221 decreased the abundance of p-Akt. In vitro study also showed that APJ antagonist, ML221 decreased AR expression. These results suggests that apelin signaling during early developmental stages might be required to stimulate the germ cell proliferation, and inhibition of apoptosis. Both in vivo and in vitro study have shown that expression of AR was regulated by apelin signaling. Since the first wave spermatogenesis involves proliferation and apoptosis, therefore, further study would be required to unravel the exact mechanism of apelin mediated regulation of testicular activity during early postnatal stages. In conclusion, the present results are an indicative of apelin mediated signaling during early postnatal stage for regulation of germ cell proliferation, apoptosis and AR expression. [Display omitted] •Expression of APJ is developmenatly regulated in mice testis.•Apelin stimulates germ cell proliferation in juvenile testis.•Apelin suppresses the apoptosis in juvenile testis.•Expression of testicular AR might be regulated apelin signaling.