The Ontogeny of Biologically Active Androgen-Binding Protein in Rat Plasma, Testis, and Epididymis*
- 1 October 1985
- journal article
- research article
- Published by The Endocrine Society in Endocrinology
- Vol. 117 (4) , 1380-1388
- https://doi.org/10.1210/endo-117-4-1380
Abstract
Androgen-binding protein (ABP) can be detected in the blood of sexually immature male rats by its ability to specifically bind [3H]5.alpha.-dihydrotestosterone (5.alpha.-DHT). Since the androgen-binding site is functional, we consider this ABP to be biologically active. ABP can be detected (641 .+-. 107 ng/ml; n =5) in plasma by the 15th day of postnatal life, it reaches a maximum concentration (1631 .+-. 323 ng/ml; n = 5) on day 20 of age, and is no longer detectable after day 40. ABP can be detected in the testes of all age groups studied (15 days to adult). However, no ABP is detectable in the epididymis until the animals are 25 days old. Plasma ABP comigrates on non-denaturing gels with photolabeled ABP from the adult or immature rat epididymis. Serum that had been treated with Affigel blue to remove albumin and with hydroxylapatite to decolorize it was photolabeled using [3H]17.beta.-hydroxy-4,6-androstadien-3-one. Photolabeled serum ABP migrated on polyacrylamide gels containing sodium dodecyl sulfate as 60,000 and 48,000 dalton androgen-specific peaks. In contrast, photolabeled adult epididymal ABP exhibited the 47,000 and 41,000 dalton peaks characteristic of ABP subunits. When photolabeled plasma and epididymal ABP were combined and electrophoresed on the same gel under denaturing conditions, prominent 60,000 and 47,000 dalton peaks were obtained, indicating that the two species of ABP retained their identities when combined. Photolabeled epididymal ABP from 25-day-old rats exhibited similar subunit mol wt in the same ratios as ABP from the adult. When epididymal ABP from the two age groups was combined and subjected to sodium dodecyl sulfate-polyacrylamide gel electrophoresis, the resulting pattern was identical to that obtained when the samples were run individually, except that there was an increase in peak height. These data indicated that there is no significant difference in the subunit mol wt of epididymal ABP from the two age groups.This publication has 19 references indexed in Scilit:
- Binding of the Photoaffinity Ligand 17β-Hydroxy-4,6- Androstadien-3-One to Rat Androgen-Binding Protein: Comparison with the Binding of 17β-Hydroxy-5α- Androstan-3-One*Endocrinology, 1980
- Preparation of 17β-hydroxy-[1ξ,2ξ-3H2]4,6-Androstadien-3-oneJournal of Labelled Compounds and Radiopharmaceuticals, 1980
- Characterization of androgen binding protein in rat epididymal cytosol using a photoaffinity ligand.Journal of Biological Chemistry, 1980
- Photoaffinity labeling of rat androgen binding protein.Proceedings of the National Academy of Sciences, 1980
- Age Related Effects on Androgen Binding Protein (ABP) in Sheep Testis and Epididymis1International Journal of Andrology, 1979
- An Androgen Binding Protein in the Testicular Cytosol of Human TestisJournal of Clinical Investigation, 1978
- ANDROGEN-BINDING PROTEIN IN THE SEMINAL PLASMA OF SOME MAMMALIAN SPECIESJournal of Endocrinology, 1978
- Immunoassay of Androgen Binding Protein in Blood: A New Approach for Study of the Seminiferous TubuleScience, 1978
- Androgen Binding Protein (ABP) in Fluids Collected from the Rete Testis and Cauda Epididymidis of Sexually Mature and Immature Rabbits and Observations on Morphological Changes in the Epididymis Following Ligation of the Ductuli Efferentes1Biology of Reproduction, 1977
- DISC ELECTROPHORESIS – II METHOD AND APPLICATION TO HUMAN SERUM PROTEINS*Annals of the New York Academy of Sciences, 1964