Richmond S A, Irving A J, Molnar E, McIlhinney R A, Michelangeli F, Henley J M, Collingridge G L
Department of Anatomy, University of Bristol, U.K.
Neuroscience. 1996 Nov;75(1):69-82. doi: 10.1016/0306-4522(96)00217-5.
The distribution of the glutamate receptor subunit GluR1 was investigated in cultured hippocampal neurons by confocal microscopy, using polyclonal antibodies directed against either the N- or C-terminal region. On living neurons, GluR1 immunofluorescence was detected with the N-terminal antibody only. GluR1 was localized in a highly punctate manner on the surface of neuronal soma and throughout the dendritic tree. Many GluR1 puncta co-localized with the synaptic marker synaptophysin, although extrasynaptic GluR1 puncta were also observed. A comparison of GluR1 subunit distribution of living neurons labelled with N-terminal antibody with that obtained after the cells had been fixed, permeabilized and subsequently reacted with C-terminal or additional N-terminal antibody showed a number of differences. In permeabilized cells additional, diffuse labelling was observed which was very pronounced in the soma and extended into the proximal dendrites. Furthermore, some spines showed little or no labelling of their membrane surface, but labelled strongly after the cells had been fixed and permeabilized. Such spines may be the postsynaptic components of silent or suboptimal synapses.
利用针对N端或C端区域的多克隆抗体,通过共聚焦显微镜研究了培养的海马神经元中谷氨酸受体亚基GluR1的分布。在活神经元上,仅用N端抗体检测到GluR1免疫荧光。GluR1以高度点状的方式定位于神经元胞体表面和整个树突树。许多GluR1点状结构与突触标记物突触素共定位,尽管也观察到了突触外的GluR1点状结构。将用N端抗体标记的活神经元的GluR1亚基分布与细胞固定、通透化并随后与C端或额外的N端抗体反应后获得的分布进行比较,发现了一些差异。在通透化细胞中,观察到额外的弥漫性标记,在胞体中非常明显并延伸到近端树突。此外,一些棘突的膜表面几乎没有或没有标记,但在细胞固定和通透化后标记强烈。这样的棘突可能是沉默或次优突触的突触后成分。