Shiraishi Mieno, Yamamoto Yoritsuna, Hirooka Nobutaka, Obuchi Yasuhiro, Tachibana Shoichi, Makishima Makoto, Tanaka Yuji
Department of General Medicine, National Defense Medical College, Tokorozawa 359-8513, Japan.
Endocr J. 2015;62(5):431-40. doi: 10.1507/endocrj.EJ14-0427. Epub 2015 Mar 16.
Although thyroid hormone is a known stimulator of erythropoietic differentiation, severe anemia is sometimes observed in patients with hyperthyroidism and this mechanism is not fully understood. The aim of this study was to investigate the effect of triiodothyronine (T3) on hemin-induced erythropoiesis. Human erythroleukemia K562 cells were used as an erythroid differentiation model. Cell differentiation was induced by hemin and the effect of pre-incubation with T3 (0.1 to 100 nM) was analyzed by measuring the benzidine-positive rate, hemoglobin content, CD71 expression (transferrin receptor), and mRNA expression for transcription factors related to erythropoiesis and thyroid hormone receptors (TRs). Hemin, a promoter of erythroid differentiation, increased the levels of mRNAs for TRα, TRβ, and retinoid X receptor α (RXRα), as well as those for nuclear factor-erythroid 2 (NFE2), GATA-binding protein 1 (GATA1) and GATA-binding protein 2 (GATA2). Lower concentrations of T3 had a stimulatory effect on hemin-induced hemoglobin production (1 and 10 nM), CD71 expression (0.1 nM), and α-globin mRNA expression (1 nM), while a higher concentration of T3 (100 nM) abrogated the stimulatory effect on these parameters. T3 at 100 nM did not affect cell viability and proliferation, suggesting that the abrogation of erythropoiesis enhancement was not due to toxicity. T3 at 100 nM also significantly inhibited expression of GATA2 and RXRα mRNA, compared to 1 nM T3. We conclude that a high concentration of T3 attenuates the classical stimulatory effect on erythropoiesis exerted by a low concentration of T3 in hemin-induced K562 cells.
尽管甲状腺激素是已知的红细胞生成分化刺激剂,但甲状腺功能亢进患者有时会出现严重贫血,而这种机制尚未完全明确。本研究的目的是探讨三碘甲状腺原氨酸(T3)对血红素诱导的红细胞生成的影响。使用人红白血病K562细胞作为红细胞分化模型。通过血红素诱导细胞分化,并通过测量联苯胺阳性率、血红蛋白含量、CD71表达(转铁蛋白受体)以及与红细胞生成和甲状腺激素受体(TRs)相关的转录因子的mRNA表达,分析预先用T3(0.1至100 nM)孵育的效果。血红素作为红细胞分化的促进剂,可增加TRα、TRβ和视黄酸X受体α(RXRα)以及核因子红细胞2(NFE2)、GATA结合蛋白1(GATA1)和GATA结合蛋白2(GATA2)的mRNA水平。较低浓度的T3对血红素诱导的血红蛋白生成(1和10 nM)、CD71表达(0.1 nM)和α-珠蛋白mRNA表达(1 nM)具有刺激作用,而较高浓度的T3(100 nM)则消除了对这些参数的刺激作用。100 nM的T3不影响细胞活力和增殖,这表明红细胞生成增强作用的消除并非由于毒性。与1 nM T3相比,100 nM的T3还显著抑制GATA2和RXRα mRNA的表达。我们得出结论,在血红素诱导的K562细胞中,高浓度的T3会减弱低浓度T3对红细胞生成的经典刺激作用。