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胸腺素在无胸腺小鼠骨髓细胞中体内外诱导末端脱氧核苷酸转移酶的产生

Induction in vivo and in vitro of terminal deoxynucleotidyl transferase by thymosin in bone marrow cells from athymic mice.

作者信息

Pazmiño N H, Ihle J N, Goldstein A L

出版信息

J Exp Med. 1978 Mar 1;147(3):708-18. doi: 10.1084/jem.147.3.708.

Abstract

Terminal deoxynucleotidyl transferase (TdT) expression in bovine serum albumin (BSA) gradient-fractionated bone marrow cells was examined in NIH Swiss nu/nu 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 nu/nu 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 nu/nu 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.

摘要

在无胸腺裸鼠(NIH Swiss nu/nu)和经胸腺切除的C57BL/6小鼠中,检测了牛血清白蛋白(BSA)梯度分离的骨髓细胞中末端脱氧核苷酸转移酶(TdT)的表达情况。在裸鼠中,TdT水平约为有胸腺同窝小鼠的10%。在C57BL/6小鼠中,胸腺切除导致骨髓细胞中TdT活性随时间逐渐丧失。为了确定骨髓中TdT表达对胸腺的明显需求是否由胸腺激素介导,我们检测了胸腺素组分5的作用。用胸腺素组分5处理NIH Swiss nu/nu或经胸腺切除的C57BL/6小鼠,可使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,25 ng/ml的胸腺素组分5诱导TdT的效果最佳,在6小时内即可出现,且放线菌素D可完全抑制这种诱导作用。该效应具有特异性,因为对照细胞和经脾脏组分5处理的细胞均未被诱导表达TdT。这些数据表明,骨髓细胞中TdT的表达受胸腺多肽激素的直接调控。

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