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生长因子、碘或δ-碘内酯对体外培养的猪甲状腺滤泡中转化生长因子β1信使核糖核酸表达的调控

Regulation of transforming growth factor beta 1 messenger ribonucleic acid expression in porcine thyroid follicles in vitro by growth factors, iodine, or delta-iodolactone.

作者信息

Gărtner R, Schopohl D, Schaefer S, Dugrillon A, Erdmann A, Toda S, Bechtner G

机构信息

Medizinische Klinik, Klinikum Innenstadt, Ludwig-Maximilians-Universitt München, Germany.

出版信息

Thyroid. 1997 Aug;7(4):633-40. doi: 10.1089/thy.1997.7.633.

Abstract

Transforming growth factor beta 1 (TGF beta 1) is an autocrine growth factor for thyrocytes and is supposed to be the mediator of iodine-induced growth inhibition of thyroid epithelial cells, but this is still controversial. We further investigated this hypothesis using intact porcine thyroid follicles ex vivo in a three-dimensional culture system. In this culture system it has been shown previously that both iodide as well as delta-iodolactone, the putative iodocompound mediating thyroid cell proliferation, inhibit growth of these follicles. We measured the amount of TGF beta 1 mRNA expression in these follicles after treatment either with thyrotropin (TSH), epidermal growth factor (EGF), or transforming growth factor alpha (TGF alpha) for growth stimulation or with inorganic iodine or delta-iodolactone in concentrations known to inhibit growth. TGF beta 1-mRNA was detected by Northern blot analysis. The known major transcript of 2.5 kb was detected in a steady state level up to 48 hours in untreated thyroid follicles. EGF and TGF alpha (5 ng/mL each) enhanced TGF beta 1 mRNA about threefold within 4 and 8 hours. This increase of TGF beta 1 mRNA was slightly decreased by simultaneous incubation with delta-iodolactone (1 microM) or iodide (40 microM KI). In contrast, both TSH (1 mU/mL) and forskolin (16 microM) decreased TGF beta 1 mRNA expression to about 70%, and this effect was abolished when follicles were pretreated with iodide (40 microM KI) in a concentration known to inhibit TSH action on cyclic adenosine monophosphate (cAMP) formation and proliferation. Iodide or delta-iodolactone alone had no significant effect on basal TGF beta 1 mRNA expression. We conclude that the growth inhibitory effect of iodide as well as of delta-iodolactone is not mediated through TGF beta 1 in intact porcine thyroid follicles ex vivo. The stimulatory effect of EGF and TGF alpha on TGF beta 1 expression might be related to extracellular matrix modulation during proliferation.

摘要

转化生长因子β1(TGFβ1)是甲状腺细胞的自分泌生长因子,被认为是碘诱导甲状腺上皮细胞生长抑制的介质,但这一点仍存在争议。我们使用完整的猪甲状腺滤泡在三维培养系统中进行体外研究,进一步探讨这一假说。在该培养系统中,先前已表明碘化物以及δ-碘内酯(推测为介导甲状腺细胞增殖的碘化合物)均可抑制这些滤泡的生长。我们在这些滤泡用促甲状腺激素(TSH)、表皮生长因子(EGF)或转化生长因子α(TGFα)刺激生长后,或用已知可抑制生长的浓度的无机碘或δ-碘内酯处理后,测量了TGFβ1 mRNA的表达量。通过Northern印迹分析检测TGFβ1-mRNA。在未处理的甲状腺滤泡中,在长达48小时的稳态水平上检测到了已知的2.5 kb主要转录本。EGF和TGFα(各5 ng/mL)在4小时和8小时内使TGFβ1 mRNA增加约三倍。与δ-碘内酯(1 μM)或碘化物(40 μM KI)同时孵育会使TGFβ1 mRNA的这种增加略有下降。相反,TSH(1 mU/mL)和福斯可林(16 μM)均使TGFβ1 mRNA表达降低至约70%,当滤泡用已知可抑制TSH对环磷酸腺苷(cAMP)形成和增殖作用的浓度的碘化物(40 μM KI)预处理时,这种作用被消除。单独的碘化物或δ-碘内酯对基础TGFβ1 mRNA表达无显著影响。我们得出结论,在体外完整的猪甲状腺滤泡中,碘化物和δ-碘内酯的生长抑制作用不是通过TGFβ1介导的。EGF和TGFα对TGFβ1表达的刺激作用可能与增殖过程中的细胞外基质调节有关。

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