Al-Hakim Abdallah, Rui Xianliang, Tsao Jennivine, Albert Paul R, Schimmer Bernard P
Department of Pharmacology, University of Toronto, Toronto, Ont., Canada M5G 1L6.
Mol Cell Endocrinol. 2004 Feb 12;214(1-2):155-65. doi: 10.1016/j.mce.2003.10.066.
Four mutant clones independently derived from the Y1 mouse adrenocortical tumor cell line have adenylyl cyclase (AC) activities that are resistant to forskolin, a direct activator of AC. In this study the AC isoform composition of the forskolin-resistant mutants was examined in order to explore the underlying basis for the resistance to forskolin. As determined by Western blot and RT-PCR analysis, the four forskolin-resistant mutants all were deficient in AC-4; the levels of other AC isoforms (AC-1, AC-3 and AC-5/6) were comparable to the levels in parent Y1 cells. Transfection of one of the mutant clones with an AC-4 expression vector increased forskolin-stimulated cAMP signaling, and restored forskolin-induced changes in cell morphology and growth. Taken together, these observations indicate that AC-4 deficiency is a hallmark of the forskolin-resistant phenotype of these mutants and suggest that AC-4 is an important target of forskolin action in the Y1 adrenal cell line.
从Y1小鼠肾上腺皮质肿瘤细胞系独立衍生出的四个突变克隆具有对福斯高林(一种腺苷酸环化酶(AC)的直接激活剂)耐药的腺苷酸环化酶活性。在本研究中,检测了对福斯高林耐药的突变体的AC同工型组成,以探究对福斯高林耐药的潜在基础。通过蛋白质印迹和逆转录-聚合酶链反应分析确定,这四个对福斯高林耐药的突变体均缺乏AC-4;其他AC同工型(AC-1、AC-3和AC-5/6)的水平与亲本Y1细胞中的水平相当。用AC-4表达载体转染其中一个突变克隆可增加福斯高林刺激的环磷酸腺苷信号传导,并恢复福斯高林诱导的细胞形态和生长变化。综上所述,这些观察结果表明AC-4缺陷是这些突变体对福斯高林耐药表型的标志,并表明AC-4是福斯高林在Y1肾上腺细胞系中作用的重要靶点。