Kawakami A, Eguchi K, Matsuoka N, Tsuboi M, Kawabe Y, Ishikawa N, Ito K, Nagataki S
First Department of Internal Medicine, Nagasaki University School of Medicine, Japan.
Endocrinology. 1996 Aug;137(8):3163-9. doi: 10.1210/endo.137.8.8754734.
The mechanisms of TSH-induced growth stimulation of thyrocytes in vivo have yet to be elucidated. We examined the antiapoptotic effect of TSH toward Fas antigen-mediated apoptosis of thyrocytes. Fas antigen was expressed on approximately 40% of unstimulated thyrocytes, and the expression was significantly inhibited by the addition of TSH in a dose-dependent manner. Treatment of thyrocytes with 8-bromo-cAMP mimicked the effect of TSH, suggesting that the inhibitory effect of TSH on Fas antigen expression was mediated by activating protein kinase A. In contrast, treatment of thyrocytes with either interleukin-1 beta (IL-1 beta) or interferon- gamma (IFN gamma) markedly increased Fas antigen expression on thyrocytes, and these effects were inhibited in the presence of TSH. The expression of the protooncogene product Bcl-2 did not change after the addition of TSH, 8-bromo-cAMP, IL-1 beta, IFN gamma, or a combination of TSH and IL-1 beta or IFN gamma. When thyrocytes stimulated with either IL-1 beta or IFN gamma were treated with anti-Fas IgM mAb, the cells were committed to apoptosis, whereas this apoptotic process was significantly inhibited by the addition of TSH. These results indicate that the Fas antigen is functionally expressed on the surface of thyrocytes, and TSH inhibits Fas antigen-mediated apoptosis of thyrocytes through the inhibitory effect of Fas antigen expression, resulting in the promotion of growth of the thyroid gland.
促甲状腺激素(TSH)在体内诱导甲状腺细胞生长刺激的机制尚未阐明。我们研究了TSH对Fas抗原介导的甲状腺细胞凋亡的抗凋亡作用。在约40%未受刺激的甲状腺细胞上表达Fas抗原,添加TSH后其表达以剂量依赖方式受到显著抑制。用8-溴-环磷酸腺苷(8-bromo-cAMP)处理甲状腺细胞模拟了TSH的作用,表明TSH对Fas抗原表达的抑制作用是通过激活蛋白激酶A介导的。相反,用白细胞介素-1β(IL-1β)或干扰素-γ(IFNγ)处理甲状腺细胞显著增加了甲状腺细胞上Fas抗原的表达,且在存在TSH的情况下这些作用受到抑制。添加TSH、8-溴-环磷酸腺苷、IL-1β、IFNγ或TSH与IL-1β或IFNγ的组合后,原癌基因产物Bcl-2的表达没有变化。当用抗Fas IgM单克隆抗体处理用IL-1β或IFNγ刺激的甲状腺细胞时,细胞发生凋亡,而添加TSH可显著抑制这一凋亡过程。这些结果表明Fas抗原在甲状腺细胞表面功能性表达,TSH通过抑制Fas抗原表达来抑制Fas抗原介导的甲状腺细胞凋亡,从而促进甲状腺的生长。