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碘抑制培养的大鼠甲状腺细胞的增殖。

Iodine inhibits the proliferation of rat thyroid cells in culture.

作者信息

Tramontano D, Veneziani B M, Lombardi A, Villone G, Ingbar S H

机构信息

Charles A. Dana Research Institute, Department of Medicine, Beth Israel Hospital, Boston, Massachusetts.

出版信息

Endocrinology. 1989 Aug;125(2):984-92. doi: 10.1210/endo-125-2-984.

Abstract

We have explored the mechanisms whereby iodine inhibits thyroid growth using as models both the FRTL5 line of rat thyroid follicular cells that require TSH for growth and the M12 line of mutant cells that grow in the absence of TSH. Between 0.01-1.0 mM, NaI produced a dose-dependent inhibition of TSH stimulation of [3H]thymidine incorporation and replication in FRTL5 cells as well as spontaneous growth in M12 cells. Iodide also inhibited the cAMP-dependent growth of FRTL5 cells induced by forskolin and (Bu)2cAMP, as well as the cAMP-independent mitogenesis induced by insulin-like growth factor-I. The effect of iodide to inhibit both TSH- and insulin-like growth factor-I-stimulated growth in FRTL5 cells was abolished by concomitant culture with methimazole, and no iodide inhibition of growth was observed in L6 myoblasts and BRL 30E hepatocytes. Exposure of cells to iodide under conditions that resulted in inhibition of TSH-stimulated growth did not significantly alter the ability of TSH to increase the intracellular cAMP concentration, nor did iodide alter two responses to TSH in FRTL5 cells that depend upon an increase in cAMP concentration: down-regulation of TSH receptor and cytoskeletal reorganization. We conclude that iodide exerts its inhibitory action on the growth of thyroid cells at multiple loci related to both the cAMP-dependent and cAMP-independent pathways of mitogenic regulation.

摘要

我们利用需要促甲状腺激素(TSH)才能生长的大鼠甲状腺滤泡细胞FRTL5系以及在无TSH情况下生长的突变细胞M12系作为模型,探索了碘抑制甲状腺生长的机制。在0.01 - 1.0 mM之间,碘化钠(NaI)对TSH刺激FRTL5细胞中[3H]胸腺嘧啶核苷掺入和复制以及M12细胞的自发生长产生剂量依赖性抑制作用。碘化物还抑制了福斯可林和(Bu)2cAMP诱导的FRTL5细胞的cAMP依赖性生长,以及胰岛素样生长因子-I诱导的cAMP非依赖性有丝分裂。通过与甲巯咪唑共同培养,碘化物抑制FRTL5细胞中TSH和胰岛素样生长因子-I刺激生长的作用被消除,并且在L6成肌细胞和BRL 30E肝细胞中未观察到碘化物对生长的抑制作用。在导致抑制TSH刺激生长的条件下,使细胞暴露于碘化物不会显著改变TSH增加细胞内cAMP浓度的能力,碘化物也不会改变FRTL5细胞中对TSH的两种依赖于cAMP浓度增加的反应:TSH受体的下调和细胞骨架重组。我们得出结论,碘化物在与有丝分裂调节的cAMP依赖性和cAMP非依赖性途径相关的多个位点对甲状腺细胞的生长发挥抑制作用。

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