Fuchs O
Institute of Hematology and Blood Transfusion, Prague, Czech Republic.
Neoplasma. 1995;42(4):179-85.
The levels of iron-responsive element-binding protein (IRE-BP I) mRNA throughout the course of erythroid differentiation were investigated in several lines of murine erythroleukemia (MEL) cells (Friend 745, 707 and Fw cells). Fw cells are not inducible for ferrochelatase activity and heme synthesis. Cytoplasmic ferrochelatase mRNA and transferrin receptor (TfR) mRNA levels are only insignificantly increased in Fw cells after induction. We have found increased levels of (IRE-BP 1) mRNA during erythroid differentiation of MEL cells of all lines investigated. Run-on transcription reactions using isolated nuclei from Friend 707 cells showed increased (IRE-BP 1) gene transcription following induction of erythroid differentiation with 5 mmol hexamethylenebisacetamide (HMBA). The increase in (IRE-BP 1) gene transcription is only about 2-fold in comparison with 8-fold increase in the level of (IRE-BP 1) mRNA during 96 hours of Friend 707 cells induction. These findings indicate that the stability of (IRE-BP 1) mRNA might also play a role in the increase of (IRE-BP 1) mRNA levels after Friend 707 cells induction. The possible role of increased (IRE-BP) mRNA levels in the elevation of TfR numbers during erythroid differentiation is discussed.
在几株小鼠红白血病(MEL)细胞系(Friend 745、707和Fw细胞)中,研究了红系分化过程中铁反应元件结合蛋白(IRE-BP I)mRNA的水平。Fw细胞的亚铁螯合酶活性和血红素合成不可诱导。诱导后,Fw细胞中的细胞质亚铁螯合酶mRNA和转铁蛋白受体(TfR)mRNA水平仅略有增加。我们发现在所有研究的MEL细胞系的红系分化过程中,(IRE-BP 1)mRNA水平均升高。使用来自Friend 707细胞的分离细胞核进行的连续转录反应显示,在用5 mmol六亚甲基双乙酰胺(HMBA)诱导红系分化后,(IRE-BP 1)基因转录增加。与Friend 707细胞诱导96小时期间(IRE-BP 1)mRNA水平增加8倍相比,(IRE-BP 1)基因转录的增加仅约2倍。这些发现表明,(IRE-BP 1)mRNA的稳定性可能也在Friend 707细胞诱导后(IRE-BP 1)mRNA水平的增加中起作用。讨论了红系分化过程中(IRE-BP)mRNA水平升高在转铁蛋白受体数量增加中的可能作用。