The cycle of foilicuiar and interstitial cells (Leydig cells) in the testis of the marbled newt, Triturus marmoratus (caudata, salamandridae)

Ultrastructural examination of the marbled newt ( Triturus marmoratus ) testis throughout the annual cycle revealed that during the period of testicular quiescence (November–February), primordial germ cells proliferate within cords of filament‐rich epithelial cells that will become follicular cells (FCs). Fibroblast‐like cells surround the FCs and form the lobule‐boundary interstitial cells (ICs). During the period of germ cell development from primordial germ cells to round spermatids (March–June), the FCs surrounding the developing germ cells contain scanty cytoplasm with abundant rough endoplasmic reticulum and scarce filaments. With spermatid elongation (July–August), the FC size grows, its nucleus becomes irregularly outlined, and its cytoplasm displays abundant smooth endoplasmic reticulum, residual bodies, lipid droplets, and large vacuoles. After spermatozoon release by the FCs (August–September), the adjacent ICs increase their size and transform into Leydig cells with abundant smooth endoplasmic reticulum, mitochondria with tubular cristae, and lipid droplets. During the period of testicular quiescence (November–February), the Leydig cells undergo involution, eventually developing the morphological attributes of mesenchymal cells. Intermingled among these cells, cords of filament‐rich cells are observed. During this period of the cycle, spermatozoon cysts supported by FCs are present. At the beginning of the germ cell proliferation period (March), these spermatozoa arc released, and the adjacent ICs undergo a transformation into Leydig cells similar to those observed in August‐September. Maturation and involution of ICs occur when testosterone levels are known to be rising and falling, respectively.