Biosynthesis and processing of ACTH/β-lipotropin was studied in Nelson's syndrome pituitary tumor tissue grown in monolayer culture. Radiolabeled peptides were immunoprecipitated and fractionated by sodium dodecyl sulfate-polyacrylamide gel electrophoresis (SDS/PAGE). Important findings include: (1) a virtual absence of 13K ACTH or 3.5K β-endorphin production; (2) evidence indicating the presence of a 24-26K ACTH and β-LPH containing intermediate (which implies a different order of processing from that reported in the mouse); (3) an extremely rapid rate of turnover and release of ACTH and β-lipotropin (β-LPH) similar to that of the mouse AtT20/D16v pituitary tumors. The latter finding is consistent with an intrinsic pituitary cell defect in the pathogenesis of this disorder.
|Original language||English (US)|
|Number of pages||3|
|Journal||Journal of Clinical Endocrinology and Metabolism|
|Publication status||Published - 1981|
ASJC Scopus subject areas
- Endocrinology, Diabetes and Metabolism