Gershengorn M C, Thaw C N
Department of Medicine, Cornell University Medical College, New York, New York.
Endocrinology. 1991 Feb;128(2):1204-6. doi: 10.1210/endo-128-2-1204.
TRH, which does not elevate cyclic AMP, and elevation of cellular cyclic AMP decrease the density (down-regulate) of TRH receptors (TRH-Rs) on pituitary (GH3) cells. In this study we measured the effects of TRH and elevation of cyclic AMP on TRH-Rs expressed in non-pituitary cells transfected with a recently cloned mouse pituitary TRH-R complementary DNA. In stably transfected rat glioma (C6-2) cells and transiently transfected COS-1 cells TRH caused TRH-R down-regulation while elevation of cyclic AMP caused increases in TRH-R density. Hence, the effects of cyclic AMP on TRH-Rs in transfected C6-2 and COS-1 cells are different from those in GH3 cells while the effects of TRH on TRH-R are similar in all three cell types. These data show that regulation of TRH-Rs is cell type specific.
促甲状腺激素释放激素(TRH)不会提高环磷酸腺苷(cAMP)水平,而细胞内cAMP水平升高会降低垂体(GH3)细胞上TRH受体(TRH-Rs)的密度(下调)。在本研究中,我们测定了TRH和cAMP水平升高对用最近克隆的小鼠垂体TRH-R互补DNA转染的非垂体细胞中表达的TRH-Rs的影响。在稳定转染的大鼠胶质瘤(C6-2)细胞和瞬时转染的COS-1细胞中,TRH导致TRH-R下调,而cAMP水平升高则导致TRH-R密度增加。因此,cAMP对转染的C6-2和COS-1细胞中TRH-Rs的影响与对GH3细胞的影响不同,而TRH对TRH-R的影响在所有三种细胞类型中相似。这些数据表明,TRH-Rs的调节具有细胞类型特异性。