Urdiales J L, Becker E, Andrieu M, Thomas A, Jullien J, van Grunsven L A, Menut S, Evan G I, Martín-Zanca D, Rudkin B B
Laboratoire de Biologie Moléculaire et Cellulaire, Unité Mixte de Recherche 49, Centre National de la Recherche Scientifique, Ecole Normale Supérieure de Lyon, 69364 Lyon Cedex 07, France.
J Neurosci. 1998 Sep 1;18(17):6767-75. doi: 10.1523/JNEUROSCI.18-17-06767.1998.
Expression of the nerve growth factor (NGF) receptors TrkA and p75(NTR) was found to vary at the surface of PC12 cells in a cell cycle phase-specific manner. This was evidenced by using flow cytometric and microscopic analysis of cell populations labeled with antibodies to the extracellular domains of both receptors. Differential expression of these receptors also was evidenced by biotinylation of surface proteins and Western analysis, using antibodies specific for the extracellular domains of TrkA and p75(NTR). TrkA is expressed most strongly at the cell surface in M and early G1 phases, whereas p75(NTR) is expressed mainly in late G1, S, and G2 phases. This expression reflects the molecular and cellular responses to NGF in specific phases of the cell cycle; in the G1 phase NGF elicits both the anti-mitogenic effect, i.e., inhibition of the G1 to S transition, and the differentiation response whereas a survival effect is provoked elsewhere in the cell cycle. A model is proposed relating these responses to the surface expression of the two receptors. These observations open the way for novel approaches to the investigation of the mechanism of NGF signal transduction.
研究发现,神经生长因子(NGF)受体TrkA和p75(NTR)在PC12细胞表面的表达随细胞周期阶段呈现特异性变化。通过对用两种受体细胞外结构域抗体标记的细胞群体进行流式细胞术和显微镜分析,证实了这一点。表面蛋白的生物素化和蛋白质免疫印迹分析(使用针对TrkA和p75(NTR)细胞外结构域的特异性抗体)也证实了这些受体的差异表达。TrkA在M期和G1早期在细胞表面表达最强,而p75(NTR)主要在G1晚期、S期和G2期表达。这种表达反映了细胞周期特定阶段对NGF的分子和细胞反应;在G1期,NGF既引发抗有丝分裂作用,即抑制G1期向S期的转变,又引发分化反应,而在细胞周期的其他阶段则引发存活效应。提出了一个将这些反应与两种受体的表面表达相关联的模型。这些观察结果为研究NGF信号转导机制开辟了新途径。