Activity Ratio Measurements Reflect Intracellular Activation of Adenosine 3′,5′-Monophosphate-Dependent Protein Kinase in Osteoblasts*
- 1 July 1982
- journal article
- research article
- Published by The Endocrine Society in Endocrinology
- Vol. 111 (1) , 178-183
- https://doi.org/10.1210/endo-111-1-178
Abstract
Parathyroid hormone, prostaglandin E2) and prostacyclin activate cAMP-dependent protein kinase in osteoblast- rich normal rat calvarial cells and in clonal rat osteogenic sarcoma cells of osteoblastic phenotype. The present study was undertaken to determine the activation of the enzyme in relation to cellular cAMP concentrations at increasing doses of the three hormones and also to test that the activity ratio measurement of the enzyme (ratio of the activity in the absence of cAMP to the activity in the presence of excess cAMP) was a true reflection of intracellular activation of the enzyme. With each hormone, using either normal or malignant osteoblasts, activation of the enzyme took place at hormone concentrations lower than those required to produce detectable changes in cAMP concentrations in the incubations. Stimulation of activity was abolished by addition of the heat-stable inhibitor of cAMP-dependent protein kinase, indicating that activation was of cAMP-dependent protein kinase alone. To demonstrate that protein kinase activation occurred intracellularly and not during sample preparation, charcoal was added at the time of cell disruption to absorb free cAMP. Under these conditions, no change was observed in the concentration of bovine parathyroid hormone required to cause activation of cAMP-dependent protein kinase. Finally, addition of purified cAMP-dependent protein kinase type I or type II to treated cells at the time of lysis did not result in significant activation of added isoenzyme, except at hormone concentrations sufficient to increase the total cAMP concentration of incubations. It is concluded that activity ratio measurement reflects the intracellular state of activation of cAMP-dependent protein kinase in the osteoblast-like cells treated by hormones and, furthermore, that only a fraction of the maximally generated cAMP is necessary for full enzyme activation.Keywords
This publication has 17 references indexed in Scilit:
- Hormonal activation of protein kinase in isolated Leydig cells. Electrophoretic analysis of cyclic AMP receptors.Journal of Biological Chemistry, 1978
- Rat osteogenic sarcoma cells: Comparison of the effects of prostaglandins E1, E2, I2 (prostacyclin), 6-keto F1α and thromboxane B2 on cyclic AMP production and adenylate cyclase activityBiochemical and Biophysical Research Communications, 1978
- Maintenance of parathyroid hormone response in clonal rat osteosarcoma linesExperimental Cell Research, 1978
- 1,25-Dihydroxycholecalciferol and Parathormone: Effects on Isolated Osteoclast-Like and Osteoblast-Like CellsScience, 1977
- Rat Osteogenic Sarcoma Cells: Isolation and Effects of Hormones on the Production of Cyclic AMP and Cyclic GMPEndocrinology, 1977
- Intermediate role of adenosine 3′:5′-cyclic monophosphate and protein kinase during gonadotropin-induced steroidogenesis in testicular interstitial cellsProceedings of the National Academy of Sciences, 1977
- Evidence for Preferential Effects of Parathyroid Hormone, Calcitonin and Adenosine on Bone and Periosteum1Endocrinology, 1977
- Parathyroid Hormone- and Prostaglandin E1-Response in a Selected Population of Bone Cells After Repeated Subculture and Storage at ‒80 CEndocrinology, 1977
- Rat osteogenic sarcoma cells: Effects of some prostaglandins, their metabolites and analogues on cyclic AMP productionProstaglandins, 1977
- Biochemical Characterization with Parathormone and Calcitonin of Isolated Bone Cells: Provisional Identification of Osteoclasts and OsteoblastsEndocrinology, 1976