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热疗对与DNA合成相关的胸苷补救的影响。

Effect of hyperthermia on thymidine salvage as related to DNA synthesis.

作者信息

Skog S, He Q, Tribukait B

机构信息

Department of Medical Radiobiology, Karolinska Institutet, Stockholm, Sweden.

出版信息

Int J Hyperthermia. 1992 Jan-Feb;8(1):99-109. doi: 10.3109/02656739209052882.

Abstract

The effect of increasing temperature up to 43 degrees C on thymidine (TdR) salvage, i.e. uptake of TdR, thymidine kinase (TK) activity, intracellular amount of thymidinetriphosphate (dTTP) and specific activity of 3H-dTTP and incorporation of dTTP into DNA, was studied in ascites tumour cells in vitro. While the uptake of [3H]TdR was almost unchanged up to 40.5 degrees C and 2.4 h followed by a decrease at later times and higher temperatures, TK activity declined already after 30 min in a temperature-dependent way, leading to a decrease in cellular amount of dTTP reaching almost undetectable values at 43 degrees C and 6.0 h. The specific activity of [3H]dTTP in the cell was elevated at 39 degrees C and 43 degrees C, but somewhat reduced at 40.5 degrees C. Incorporation into DNA of [3H]TdR decreased in a temperature-dependent way with increasing incubation time. After correction for specific activity of [3H]dTTP, however, the incorporation of [3H]TdR into DNA at 39 degrees C and 40.5 degrees C was unchanged up to 2.4 h and for 40.5 degrees C up to 6.0 h, while incorporation into DNA at 43 degrees C was still reduced. The overall protein synthesis was also reduced in a temperature-dependent way. We concluded that phosphorylation of TdR to dTMP was more sensitive to moderately elevated temperatures than uptake of TdR and DNA synthesis per se, caused by a reduced TK activity. The decline in TK activity was probably due to a decrease in TK polypeptide synthesis.

摘要

研究了在体外腹水肿瘤细胞中,将温度升高至43摄氏度对胸苷(TdR)补救途径(即TdR摄取)、胸苷激酶(TK)活性、细胞内三磷酸胸苷(dTTP)含量、3H-dTTP比活性以及dTTP掺入DNA的影响。在40.5摄氏度及2.4小时内,[3H]TdR的摄取几乎没有变化,随后在更高温度及更晚时间出现下降;而TK活性在30分钟后就已经以温度依赖的方式下降,导致细胞内dTTP含量减少,在43摄氏度及6.0小时时几乎降至检测不到的值。细胞内[3H]dTTP的比活性在39摄氏度和43摄氏度时升高,但在40.5摄氏度时略有降低。[3H]TdR掺入DNA的量随孵育时间增加而以温度依赖的方式减少。然而,校正[3H]dTTP的比活性后,在39摄氏度和40.5摄氏度时,[3H]TdR掺入DNA在2.4小时内保持不变,在40.5摄氏度时直至6.0小时保持不变,而在43摄氏度时掺入DNA的量仍减少。总的蛋白质合成也以温度依赖的方式减少。我们得出结论,TdR磷酸化为dTMP对适度升高的温度比TdR摄取和DNA合成本身更敏感,这是由于TK活性降低所致。TK活性的下降可能是由于TK多肽合成减少。

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