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Thymidylate synthetase and dihydrofolic acid reductase in the stimulated human lymphocyte

โœ Scribed by Farid I. Haurani; Carl G. Kardinal; William A. Biermann


Publisher
John Wiley and Sons
Year
1978
Tongue
English
Weight
656 KB
Volume
95
Category
Article
ISSN
0021-9541

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โœฆ Synopsis


The phytohemagglutinin (PHAI-stimulated human lymphocytes demonstrated trace or no activity of (dihydro) folate acid reductase using three methods including a radioassay, but demonstrated ample activity of thymidylate synthetase. This was true regardless of the day of harvest, (first through seventh) of the stimulated lymphocyte. The lymphocyte extracts revealed no inhibitor to the reductase enzyme when these extracts were added before the liver extracts to the assay system. When methotrexate (MTX) was added to the culture media of the lymphocytes, there was, as expected, an increase in the synthetase activity, but the expected rise in the reductase activity did not occur, it remained nil. On the other hand, MTX did influence the incorporation of nucleosides by the stimulated lymphocytes in a fashion similar to its action on the incorporation of the same nucleosides by other cells.

Several of the folate-related enzymes have been investigated in human tissues, particularly in the blood and bone marrow cells. The effects of antimetabolites, methotrexate (MTX) in particular, on the DNA synthesis of normal or leukemic cells have also been the subject of various studies (Bertino et al., '65;


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โœ Carlos Santiago; Mark Collins; Lee F. Johnson ๐Ÿ“‚ Article ๐Ÿ“… 1984 ๐Ÿ› John Wiley and Sons ๐ŸŒ English โš– 849 KB

We have studied the rate of transcription of t h e gene for dihydrofolate reductase (DHFR) in mouse 3T6 fibroblasts during serum-induced transitions between the resting (Go) and growing states. As a model system, we have used a methotrexate-resistant 3T6 cell line that overproduces DHFR and its mRNA