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维甲酸抑制培养的人甲状腺细胞中人类甲状腺过氧化物酶和甲状腺球蛋白基因的表达。

Retinoic acid inhibits human thyroid peroxidase and thyroglobulin gene expression in cultured human thyrocytes.

作者信息

Namba H, Yamashita S, Morita S, Villadolid M C, Kimura H, Yokoyama N, Izumi M, Ishikawa N, Ito K, Nagataki S

机构信息

First Department of Internal Medicine, Nagasaki University School of Medicine, Japan.

出版信息

J Endocrinol Invest. 1993 Feb;16(2):87-93. doi: 10.1007/BF03347654.

Abstract

The effect of retinoic acid (RA) on thyroid peroxidase (TPO) and thyroglobulin (Tg) gene expression was investigated in cultured human thyrocytes. Thyrocytes dispersed from Graves' thyroid tissues were incubated with TSH 5mU/ml and RA 0, 0.01, 0.1, 1.0 microM for 72 h respectively. The samples were then subjected to Northern gel analysis. Northern gel analysis using the specific cDNA probes showed that RA suppressed the accumulation of TPO and Tg mRNA stimulated by TSH in a time- and dose-responsive manner. Furthermore, RA inhibited forskolin and 8-Bromo-cyclic-AMP-induced TPO and Tg gene expression, suggesting a distal action site for these cAMP mediated gene expressions. Immunoprecipitation analysis using the specific monoclonal antibodies showed that TSH increased newly synthesized 100, 75, 36-kDa [35S] TPO. The increased de novo TPO was markedly inhibited by RA. Tg secretion from monolayer cultures was measured by radioimmunoassay. RA also inhibited TSH-induced Tg secretion in a dose dependent manner. RA did not affect [3H] thymidine uptake into primary cultured human thyrocytes. In conclusion, RA inhibits the synthesis of TPO and Tg via the suppression of thyroid-specific gene expression although the exact site of RA action on these genes in human thyroids remains to be further elucidated. These results suggest that RA may play a regulatory role in Tg and TPO gene expression, subsequently resulting in the suppression of thyroid hormone synthesis.

摘要

在培养的人甲状腺细胞中研究了视黄酸(RA)对甲状腺过氧化物酶(TPO)和甲状腺球蛋白(Tg)基因表达的影响。将从格雷夫斯甲状腺组织中分离出的甲状腺细胞分别与5mU/ml促甲状腺激素(TSH)和0、0.01、0.1、1.0μM的RA孵育72小时。然后对样本进行Northern凝胶分析。使用特异性cDNA探针进行的Northern凝胶分析表明,RA以时间和剂量响应的方式抑制了TSH刺激的TPO和Tg mRNA的积累。此外,RA抑制了福斯可林和8-溴环磷酸腺苷诱导的TPO和Tg基因表达,提示这些环磷酸腺苷介导的基因表达存在远端作用位点。使用特异性单克隆抗体进行的免疫沉淀分析表明,TSH增加了新合成的100、75、36kDa的[35S]TPO。RA显著抑制了从头合成的TPO的增加。通过放射免疫测定法测量单层培养物中Tg的分泌。RA也以剂量依赖性方式抑制TSH诱导的Tg分泌。RA不影响[3H]胸苷对原代培养的人甲状腺细胞的摄取。总之,RA通过抑制甲状腺特异性基因表达来抑制TPO和Tg的合成,尽管RA在人甲状腺中对这些基因的确切作用位点仍有待进一步阐明。这些结果表明,RA可能在Tg和TPO基因表达中发挥调节作用,随后导致甲状腺激素合成受到抑制。

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