Dolzhanskaya Natalia, Merz George, Denman Robert B
Biochemical Molecular Neurobiology Laboratory, Department of Molecular Biology, New York State Institute for Basic Research in Developmental Disabilities, 1050 Forest Hill Road, Staten Island, NY 10314, USA.
Brain Res. 2006 Sep 27;1112(1):56-64. doi: 10.1016/j.brainres.2006.07.026. Epub 2006 Aug 17.
PC12 cells are a well-known model of parasympathetic neurons. They have also been used to study the dynamics of heterologously expressed fragile X mental retardation (FMRP) granule trafficking down neurites. Here, we demonstrate that undifferentiated and differentiated PC12 cells harbor endogenous FMRP-containing granules. These granules are not stress granules because they do not associate with an authentic stress granule marker protein T-cell internal antigen 1 (TIA-1). Treatment with sodium arsenite induces stress granule formation in undifferentiated and differentiated PC12 cells. In NGF-treated cells, FMRP-containing stress granules are observed in the soma, neurites and growth cones by co-immunostaining with anti-TIA-1 antibody. These data demonstrate that all three microdomains respond similarly to oxidative stress. Nevertheless, we find significantly less co-localization of FMRP and TIA-1 and FMRP and its homologs in the neurites of differentiated PC12 cells treated with sodium arsenite than in the soma or growth cones. The heterogeneity of these granules suggests that FMRP has multiple roles in neurites.
PC12细胞是一种著名的副交感神经元模型。它们也被用于研究异源表达的脆性X智力低下(FMRP)颗粒沿神经突运输的动力学。在此,我们证明未分化和分化的PC12细胞含有内源性含FMRP的颗粒。这些颗粒不是应激颗粒,因为它们不与真正的应激颗粒标记蛋白T细胞内抗原1(TIA-1)相关联。亚砷酸钠处理可诱导未分化和分化的PC12细胞形成应激颗粒。在经神经生长因子(NGF)处理的细胞中,通过与抗TIA-1抗体共免疫染色,在胞体、神经突和生长锥中观察到含FMRP的应激颗粒。这些数据表明,所有三个微区对氧化应激的反应相似。然而,我们发现,与胞体或生长锥相比,经亚砷酸钠处理的分化PC12细胞的神经突中FMRP与TIA-1以及FMRP与其同源物的共定位明显减少。这些颗粒的异质性表明FMRP在神经突中具有多种作用。