Morales C R, Alcivar A A, Hecht N B, Griswold M D
Program in Biochemistry and Biophysics, Washington State University, Pullman 99164-4660.
Mol Endocrinol. 1989 Apr;3(4):725-33. doi: 10.1210/mend-3-4-725.
A treatment which used vitamin A depletion followed by vitamin A repletion was used to synchronize seminiferous tubules to a few related stages of the cycle of the seminiferous epithelium. The success of the synchronization procedure was dependent on the age and size of the rat at the initiation of the experiment (20 days of age and 35-40 g) and the extent to which the vitamin A deficiency had progressed. Administration of retinol was done when the only viable germinal cells in the testis were preleptotene spermatocytes and type A spermatogonia but if the deficiency was prolonged spermatogenesis did not recover. Once established synchrony appeared to be sustained at least through several consecutive cycles. A combination of molecular probes was used to determine if the synchronized testes displayed stage specific variations in Sertoli cell and germinal cell mRNA levels as has been reported for normal asynchronized rats. Sertoli cells in the synchronized testes were shown by quantitative in situ hybridization and by Northern blot analysis to have stage specific variations in the levels of mRNA for transferrin, sulfated glycoprotein-1, and sulfated glycoprotein-2. The mRNA levels in the different stages were qualitatively similar to those in equivalent stages previously reported for testes from asynchronous rats. The germinal cell content of the synchronized testes were examined with Northern blots probed with nick-translated protamine 1 and transition protein 1 cDNAs.(ABSTRACT TRUNCATED AT 250 WORDS)
