首页> 美国卫生研究院文献>The Journal of Experimental Medicine >Induction in vivo and in vitro of terminal deoxynucleotidyl transferase by thymosin in bone marrow cells from athymic mice
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Induction in vivo and in vitro of terminal deoxynucleotidyl transferase by thymosin in bone marrow cells from athymic mice

机译:胸腺肽在无胸腺小鼠骨髓细胞中体内和体外诱导末端脱氧核苷酸转移酶

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摘要

Terminal deoxynucleotidyl transferase (TdT) expression in bovine serum albumin (BSA) gradient-fractionated bone marrow cells was examined in NIH Swiss nuu and thymectomized C57BL/6 mice. In nude mice, TdT levels were approximately 10% of those of thymus-bearing littermates. In C57BL/6 mice, thymectomy caused a time-dependent loss of TdT activity in bone marrow cells. To determine whether or not not the apparent thymic requirement for TdT expression in bone marrow was mediated by thymic hormones, we examined the effects of thymosin fraction 5. Treatment of either NIH Swiss nuu or thymectomized C57BL/6 mice with thymosin fraction 5 restored the levels of TdT activity in BSA gradient-fractionated bone marrow cells to normal. Moreover, treatment of BSA gradient-fractionated bone marrow cells from NIH Swiss nuu or thymectomized C57BL/6 mice in tissue culture with thymosin fraction 5 induced TdT expression. In tissue culture, TdT induction was optimal with 25 ng/ml of thymosin fraction 5, it occurred within 6 h, and it was completely inhibited by actinomycin D. The effect was specific in that neither control nor spleen fraction 5- treated cells were induced to express TdT. These data demonstrate that TdT expression in bone marrow cells is under the direct control of thymic polypeptide hormones.
机译:在NIH Swiss nu / nu和经胸腺切除的C57BL / 6小鼠中检查了牛血清白蛋白(BSA)梯度分离的骨髓细胞中的末端脱氧核苷酸转移酶(TdT)表达。在裸鼠中,TdT水平约为带有胸腺的同窝仔的TdT水平的10%。在C57BL / 6小鼠中,胸腺切除术导致骨髓细胞中TdT活性随时间的流逝。为了确定是否通过胸腺激素介导了骨髓中TdT表达的明显胸腺需求,我们检查了胸腺素组分5的作用。恢复了胸腺素组分5对NIH Swiss nu / nu或经胸腺切除的C57BL / 6小鼠的治疗BSA梯度分离的骨髓细胞中TdT活性水平恢复正常。此外,在组织培养中用胸腺素组分5处理来自NIH Swiss nu / nu或经胸腺切除的C57BL / 6小鼠的BSA梯度分离的骨髓细胞,可诱导TdT表达。在组织培养中,用25 ng / ml胸腺素5级分诱导TdT最佳,在6小时内发生,并且被放线菌素D完全抑制。该作用的特异性在于,既不诱导对照也不经脾5级处理的细胞被诱导表达TdT。这些数据表明,TdT在骨髓细胞中的表达受胸腺多肽激素的直接控制。

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