Meisinger C, Hertenstein A, Grothe C
Institute of Anatomy, University of Freiburg, Germany.
Brain Res Mol Brain Res. 1996 Feb;36(1):70-8. doi: 10.1016/0169-328x(95)00246-o.
In the present study we have analyzed the expression of fibroblast growth factor receptor 1 (FGFR-1) mRNA in the developing and adult rat adrenal gland and in PC12 cells under different culture conditions. For this purpose a sensitive ribonuclease protection assay using 33P-labelled riboprobes was established. 33P-labelled riboprobes show a high resolution and are relatively easy to handle. FGFR-1 mRNA was found to be present in the postnatal and adult adrenal gland. In the cortex high levels of FGFR-1 mRNA were detected at postnatal day (P) 1 and P8, during the third week the mRNA levels declined, and reached low levels during adulthood. PC12 cells also contained detectable amounts of FGFR-1 mRNA. With the exception of NGF, however, the different treatment procedures did not affect FGFR-1 mRNA levels. The expression pattern of the FGFR-1 transcript matches that of the expression of FGF-2 and of the mitotic activity in the developing and adult cortex. This supports the idea that FGF-2 might act as an autocrine mitogen for adrenocortical cells. In the medulla FGFR-1 mRNA levels were low at the first 3 postnatal weeks and increased towards the adult. In accordance with the developing expression pattern of FGF-2 in the medulla and in vitro effects of this protein on chromaffin and PC12 cells an autocrine/paracrine role as a maintenance and differentiation factor for chromaffin cells is conceivable.
在本研究中,我们分析了成纤维细胞生长因子受体1(FGFR-1)mRNA在发育中和成年大鼠肾上腺以及不同培养条件下的PC12细胞中的表达。为此,建立了一种使用33P标记核糖探针的灵敏核糖核酸酶保护测定法。33P标记的核糖探针具有高分辨率且相对易于操作。发现FGFR-1 mRNA存在于出生后和成年肾上腺中。在皮质中,出生后第1天(P1)和第8天检测到高水平的FGFR-1 mRNA,在第三周mRNA水平下降,成年期达到低水平。PC12细胞也含有可检测量的FGFR-1 mRNA。然而,除了神经生长因子(NGF)外,不同的处理程序并未影响FGFR-1 mRNA水平。FGFR-1转录本的表达模式与发育中和成年皮质中FGF-2的表达以及有丝分裂活性的表达模式相匹配。这支持了FGF-2可能作为肾上腺皮质细胞自分泌有丝分裂原的观点。在髓质中,出生后前三周FGFR-1 mRNA水平较低,成年期升高。根据髓质中FGF-2的发育表达模式以及该蛋白对嗜铬细胞和PC12细胞的体外作用,可以设想其作为嗜铬细胞维持和分化因子的自分泌/旁分泌作用。