Expression of Connexin43 in mouse Leydig, Sertoli, and germinal cells at different stages of postnatal development

• Published in: The Anatomical record Vol. 264; no. 1; pp. 13 - 24
• Main Authors: Bravo‐Moreno, J. Francisco, Díaz‐Sánchez, Vicente, Montoya‐Flores, José G., Lamoyi, Edmundo, Saéz, Juan C., Pérez‐Armendariz, E. Martha
• Format: Journal Article
• Language: English
• Published: New York John Wiley & Sons, Inc 01.09.2001
• Subjects: 3-Hydroxysteroid Dehydrogenases - metabolism; Aging - metabolism; Animals; Animals, Newborn - growth & development; Animals, Newborn - metabolism; Connexin 43 - metabolism; Cx43; development; differentiation; Extracellular Space - metabolism; Germ Cells - metabolism; germinal; Immunohistochemistry; Leydig; Leydig Cells - metabolism; Male; Mice - metabolism; Mice, Inbred Strains; Multienzyme Complexes - metabolism; Osmolar Concentration; Progesterone Reductase - metabolism; proliferation; secretion; Sertoli; Sertoli Cells - metabolism; Steroid Isomerases - metabolism; Testis - growth & development; Testis - metabolism; Testosterone - metabolism
• ISSN: 0003-276X; 1097-0185
• DOI: 10.1002/ar.1100

Connexin 43 (Cx43) is the most abundant and ubiquitously distributed gap junction protein in testicular cells. Lack of Cx43 expression results in male infertility. We investigated whether Cx43 is expressed and regulated in Leydig, Sertoli and germinal cells at different stages of postnatal development. Cx43 was detected using three different antibodies shown by immunoblotting to be highly specific. At different postnatal ages Cx43 localization was compared in serial or double labeled testicular cryosections with immunocytochemical distribution of steroidogenic enzyme, 3 βhidroxysteroid‐dehydrogenase (3βHSD), Mullerian inhibitory hormone (MIH), and germinal nuclear cell antigen (GNCA1), which are specific markers of interstitial Leydig, Sertoli and germinal cells, respectively. In the interstitium, round cell clumps (RCC) with lipid droplets positive for 3βHSD and Cx43 were frequently found at intertubular areas at birth and Cx43 was mainly localized at cell membrane appositions. From day 3, the number and size of 3βHSD‐positive RCC started to decrease, and reached a minimum at 7–14 dpp; Cx43 expressed by them is progressively downregulated. From day 21 an increase in the size and number of RCC positive for Cx43 and 3βHSD was found that continued at 24, 26 and 28 days and reached a maximum at 35 and 60 dpp. Biphasic expression of interstitial Cx43 and 3βHSD was also found to be positively and temporally correlated with fluctuations in intratesticular testosterone content at all ages studied. In the seminiferous cord (SC), Cx43 was expressed at birth between adjacent Sertoli cells (MIH positive) localized at the periphery, as well as in their cytoplasm projections that surround centrally localized gonocytes. From days 3 to 7, Cx43 labeling increased in Sertoli cells mainly at their apical border. At day 14, Cx43 distribution in Sertoli cells changed from apical to basal in parallel to migration of germinal (GNCA1‐positive) cells from the periphery to the center of the SC. At all these ages, Cx43 was also localized at cell borders between Sertoli and germinal cells. In conclusion, this study demonstrates that Cx43 in Leydig cells is regulated during postnatal development in an age and functional dependent manner. In the tubule, it is demonstrated that Cx43 is modulated in Sertoli cells during the neonatal and prepubertal period. We also provide evidence for the first time that Cx43‐gap junctions communicate between Sertoli and germinal cells before and during the first wave of spermatogenesis. Anat Rec 264:13–24, 2001. © 2001 Wiley‐Liss, Inc.