Hutton L A, deVellis J, Perez-Polo J R
Department of Human Biological Chemistry and Genetics, University of Texas Medical Branch, Galveston 77555.
J Neurosci Res. 1992 Jul;32(3):375-83. doi: 10.1002/jnr.490320309.
Using a quantitative reverse transcription-polymerase chain reaction (RT-PCR) we have investigated the expression of the neurotrophin receptors p75NGFR, trkA, and trkB mRNAs in cultures of rat pup type I astrocytes and in the C6 rat glioma cell line. All three neurotrophin receptor mRNAs are expressed in both C6 cells and in type I astrocytic cultures. p75NGFR mRNA levels are increased by either cycloheximide or nerve growth factor (NGF) treatment of C6 cells as measured using RT-PCR. Type I astrocyte cultures also expressed p75NGFR mRNA and NGF treatment increased p75NGFR mRNA levels in these cultures. TrkB mRNA levels were increased by cycloheximide treatment of type I astrocyte cultures but not by NGF treatment. Using RT-PCR, trkA mRNA was detected in astrocytic cultures as well as in the rat C6 and PC-12 cell lines. We conclude that cultures of type I astrocytes express active NGF receptors and that glia can elicit a response to NGF as seen by an increase in p75NGFR mRNA levels following exposure to NGF.
我们运用定量逆转录-聚合酶链反应(RT-PCR),研究了大鼠幼崽I型星形胶质细胞培养物以及C6大鼠胶质瘤细胞系中神经营养因子受体p75NGFR、trkA和trkB mRNA的表达情况。在C6细胞和I型星形胶质细胞培养物中均表达了所有这三种神经营养因子受体mRNA。通过RT-PCR检测发现,用放线菌酮或神经生长因子(NGF)处理C6细胞后,p75NGFR mRNA水平升高。I型星形胶质细胞培养物也表达p75NGFR mRNA,NGF处理可使这些培养物中的p75NGFR mRNA水平升高。用放线菌酮处理I型星形胶质细胞培养物可使TrkB mRNA水平升高,但NGF处理则无此作用。通过RT-PCR,在星形胶质细胞培养物以及大鼠C6和PC-12细胞系中均检测到了trkA mRNA。我们得出结论,I型星形胶质细胞培养物表达活性NGF受体,并且如暴露于NGF后p75NGFR mRNA水平升高所示,神经胶质细胞能够对NGF产生反应。