Acute and temporary inhibition of thymidine kinase in mouse bone marrow cells after low-dose exposure

• Published in: International journal of radiation biology and related studies in physics, chemistry and medicine Vol. 45; no. 3; p. 205
• Main Authors: Feinendegen, L E, Mühlensiepen, H, Lindberg, C, Marx, J, Porschen, W, Booz, J
• Format: Journal Article
• Language: English
• Published: England 01.01.1984
• Subjects: Animals; Bone Marrow - enzymology; Bone Marrow - radiation effects; Cesium Radioisotopes; Dose-Response Relationship, Radiation; Female; Gamma Rays; Mice; Thymidine Kinase - metabolism; Time Factors; Whole-Body Irradiation
• ISSN: 0020-7616
• DOI: 10.1080/09553008414550301

Low-dose whole-body exposure of mice to less than 0.01 Gy gamma-rays causes inhibition of incorporation of thymidine or 5-iodo-2-deoxyuridine into DNA of bone-marrow cells in vitro; the effect is maximal in cells at 4 hours after exposure and then subsides within about 10 hours. This is due to the inhibition of cellular thymidine kinase, which gradually develops to a maximum at 4 hours after exposure and again subsides within the next 10 hours. This inhibition involves only 35 per cent of the entire cellular enzyme activity and, analogous to the depression of thymidine incorporation into the cells, is only seen when the cells are collected into medium that is buffered to 7.2-7.4 and contains about 1350 mg NaHCO3 per litre. Addition of NaHCO3 to the cell homogenate or to the high speed supernatant containing the enzyme, but not to intact cells, failed to produce enzyme inhibition. There is also no depression of 5-iodo-2-deoxyuridine uptake into the intact cells in vitro when the mice are irradiated either shortly before or after i.v. injection of 0.02 mg of procain chloride. The reversibility of the effect in vivo and in vitro suggests a particular enzyme control mechanism that may be non-specifically triggered by intracellular charges, such as peroxides, and may enhance repair.