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地塞米松对二甲基亚砜诱导的转谷氨酰胺酶活性及白血病细胞分化的抑制作用。

Dexamethasone inhibition of DMSO-induced transglutaminase activity and differentiation of leukemic cells.

作者信息

Hsu K H, Friedman H

出版信息

Proc Soc Exp Biol Med. 1984 Feb;175(2):205-10. doi: 10.3181/00379727-175-41789.

Abstract

Treatment of the Friend erythroleukemic (FL) cell line GM979 with dimethyl sulfoxide (DMSO) or n-butyric acid induced erythroid differentiation. Transglutaminase (TGase) activity also increased in these treated cells. Glucocortical steroids, i.e., dexamethasone (DEX) and triamcinolone acetonide, when added to the cultured medium, inhibited the DMSO-induced hemoglobin synthesis but not n-butyric acid-induced hemoglobin synthesis. Similarly, these steroids inhibited DMSO-increased TGase activity but not n-butyric acid-increased TGase activity in intact FL cells. Neither the differentiation-inducing agents nor the steroids had any effect on TGase activity when they were directly added to cell lysates. These results support the view that the increase of TGase activity may be related to erythroid differentiation of FL cells and of its possible role of this enzyme in FL cell-induced differentiation.

摘要

用二甲基亚砜(DMSO)或正丁酸处理弗瑞德红白血病(FL)细胞系GM979可诱导红系分化。这些处理过的细胞中转谷氨酰胺酶(TGase)活性也增加。当向培养基中添加糖皮质激素,即地塞米松(DEX)和曲安奈德时,可抑制DMSO诱导的血红蛋白合成,但不抑制正丁酸诱导的血红蛋白合成。同样,这些类固醇在完整的FL细胞中可抑制DMSO增加的TGase活性,但不抑制正丁酸增加的TGase活性。当将诱导分化剂和类固醇直接添加到细胞裂解物中时,它们对TGase活性均无影响。这些结果支持以下观点,即TGase活性的增加可能与FL细胞的红系分化有关,以及该酶在FL细胞诱导分化中可能发挥作用。

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