Application of an ELISA procedure for the quantitation of bromodeoxyuridine incorporated into cellular DNA.

We have developed a sensitive enzyme-linked immunosorbent assay (ELISA) procedure that uses a commercially-available anti-BrdUrd antibody for the quantitation of BrdUrd substituted into DNA. In our assay, 50% displacement occurs at 0.89 nM of BrdUrd in 2.

Cushing's syndrome due to bilateral adrenal macronodular hyperplasia with undetectable ACTH: cell culture of adenoma cells on extracellular matrix.

A 59-year-old man developed Cushing's syndrome with massive bilateral adrenal macronodular hyperplasia. Plasma ACTH levels were undetectable both peripherally and in the inferior petrosal sinus. Computed tomography scans of his pituitary were normal.

Inhibition of O6-alkylguanine-DNA-alkyltransferase activity potentiates cytotoxicity and induction of SCEs in human glioma cells resistant to 1,3-bis(2-chloroethyl)-1-nitrosourea.

SF-188 is a human glioma-derived cell line resistant to the cytotoxic effects of and the induction of sister chromatid exchanges (SCEs) by 1,3-bis(2-chloroethyl)-1-nitrosourea (BCNU). Pretreatment of SF-188 cells with N-methyl-N-nitrosourea (MNU) for 1 h increased the cytotoxicity of a 1-h treatment with BCNU 2- to 10-fold and doubled the number of SCEs; the magnitude of these effects was dependent on the dose of both agents. Treatment of SF-188 cells with MNU resulted in a dose-dependent inhibition of O6-alkylguanine-DNA-alkyltransferase (O6-AT) activity.

Purification of rat adrenocortical actin and its use in an immunoprecipitation assay to quantitate cellular actin.

In an earlier study on the long-term effects of the pituitary hormone corticotropin (adrenocorticotropin, ACTH), we reported that ACTH promotes the loss of 20-25% of the total actin in isolated rat adrenocortical cells. In a continuation of this work, we report here the purification to near homogeneity of rat adrenal actin. We demonstrate that the protein purified is adrenal actin, and use this actin in the DNAase immunoprecipitation assay of Snabes et al.

The role of extracellular calcium in corticotropin-stimulated steroidogenesis.

The role of extracellular Ca2+ in the binding of corticotropin (ACTH) to adrenocortical cell receptors as well as in the post-binding events involved in steroidogenesis were investigated. Binding studies using [125I-Tyr23,Phe2,Nle4]ACTH (1-38) peptide showed that extracellular Ca2+ is essential not only for the interaction of ACTH with its receptor, but also for continued occupancy of the receptor. In view of the requirement of Ca2+ for binding the hormone to the receptor, the role of Ca2+ in post-receptor events was investigated by covalently attaching the hormone to its receptor by photoaffinity labeling in the presence of Ca2+.