Metallothionein (MT) in the human male excretory ducts of the testis, such as the tubuli seminiferi recti, rete testis, ductuli efferentes, ductus epididymidis, and ductus deferens was examined immunohistochemically in 15 patients (one, testicular injury; one, testicular torsion; six, testicular tumor; seven, prostate cancer). The immunoreaction for MT was identified in Sertoli cells of the tubuli recti, and in the epithelial cells of rete testis, ductuli efferentes, ductus epididymidis at the tail portion, and ductus deferens near the epididymal tail. The immunoreaction in the tail was found mainly in the principal cells, and the secretory products near the surface of epithelial cells, and in the lumen. The MT immunoreaction in the epididymal head and body was observed to occur in the basal cells only. This result suggested that the epithelial cells have a different physiological function among the various portions of the excretory ducts of human testis.Metallothionein (MT) is known as being a metalbinding protein with a low molecular weight of approximately 6,000 Daltons and is rich in cysteine and sulfur (5). It is unique in its ability to bind class II-B metals, such as zinc, and has been identified in the seminiferous tubules and prostate (3,8,10,13). MT was also shown to secrete in the prostatic fluid and was thought to interact with mature sperm (11), but the role of MT in the human male reproductive tract, especially in the epididymis, has not yet been elucidated. Therefore, we attempted to demonstrate the localization of MT in the human male excretory ducts of the testis.
MATERIALSAND METHODS
Tissue preparation for immunohistochemical studiesThe tissue samples were taken from the testis, epididymis, and spermatic cord obtained from 15 patients. Two patients had undergone orchiectomy following testicular torsion and injury (both were 20 years old), six had testicular tumors (ages 27 to 41 years), and seven had prostate cancer (ages 69 to 89 years). The tissues were fixed in Bouin solution for 24 hr or in 10% buffered formalin solution for 24-48 hr before being embedded in paraffin. They were then cut at a thickness of 3 pm and mounted on poly-L-lysine coated glass slides for immunohistochemical staining. All sections for histological examination were stained by hematoxylin and eosin.
Preparation of anti-MT-1 antibodyAnti-rat MT-1 antibody was prepared by first