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IRON UPTAKE IN CULTURED SCHWANN CELLS. EVIDENCE FOR A NON TRANSFERRIN MEDIATED PATHWAY

机译:在培养的施万细胞中摄取铁。非运铁蛋白介导途径的证据

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Schwann cells (SCs) synthesize the myelin sheath in the peripheral nervous system. We have previously described that Fe~(3+) and holotransferrin (hTf) prevent SCs from dedifferentiation through the cAMP/protein kinase A pathway. A major route for the delivery of iron to the cells is the receptor mediated import although a non-Tf mediated pathway has also been described. The aim of the present work is to study the effect of serum deprivation on the kinetics of iron uptake. Cultured SCs were submitted to serum deprivation and supplemented with Fe~(3+), aTf, hTf for 3,6,24 and 72 hs in the presence of ~(59)Fe (FeCl_3). Intracellular iron content was measured by atomic absorption. The presence of Tf receptors (TfR) was evaluated by western blot. Our results demonstrate that there is no uptake of ~(59)Fe in the cells incubated in the presence of serum or apoTf. However, in the cells supplemented with Fe~(3+) or hTf the uptake of ~(59)Fe increases from 1 h to 24hs. These results agree with those referred to intracellular iron content. Deferroxamine blocks the effects promoted by Fe~(3+) or hTf. The expression of TfR increased in SCs submitted to serum deprivation. The supplementation with aTf decreases TfR levels to 66% while hTf supplementation decreases levels to 30%. Our results suggest the existence of an iron uptake mechanism independent of Tf which SCs would express when submitted to a harsh environment.
机译:雪旺氏细胞(SCs)在周围神经系统中合成髓鞘。先前我们已经描述了Fe〜(3+)和全运铁蛋白(hTf)阻止SC通过cAMP /蛋白激酶A途径去分化。铁转运至细胞的主要途径是受体介导的输入,尽管也已描述了非Tf介导的途径。本工作的目的是研究血清剥夺对铁摄取动力学的影响。培养的SCs进行血清剥夺,并在〜(59)Fe(FeCl_3)存在下补充Fe〜(3 +),aTf,hTf 3、6、24和72 h。细胞内铁含量通过原子吸收来测量。通过蛋白质印迹评估Tf受体(TfR)的存在。我们的结果表明,在存在血清或载脂蛋白Tf的情况下孵育的细胞中不吸收〜(59)Fe。然而,在补充有Fe〜(3+)或hTf的细胞中,〜(59)Fe的摄取从1小时增加到24小时。这些结果与关于细胞内铁含量的那些结果一致。去铁胺阻断了Fe〜(3+)或hTf促进的作用。 TfR的表达在提交血清剥夺的SC中增加。补充aTf可将TfR水平降低至66%,而hTf补充可将水平降低至30%。我们的研究结果表明,铁的吸收机制与Tf无关,而SC会在恶劣环境下表现出来。

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