Menco B P, Cunningham A M, Qasba P, Levy N, Reed R R
Department of Neurobiology and Physiology, Northwestern University, Evanston, IL 60208-3520, USA.
J Neurocytol. 1997 Oct;26(10):691-706. doi: 10.1023/a:1018554029186.
Two different polyclonal antibodies were raised to synthetic peptides corresponding to distinct putative odour receptors of rat and mouse. Both antibodies selectively labelled olfactory cilia as seen with cryofixation and immunogold ultrastructural procedures. Regions of the olfactory organ where label was detected were consistent with those found at LM levels. Immunopositive cells were rare; only up to about 0.4% of these receptor cells were labelled. Despite chemical, species, and topographic differences both antibodies behaved identically in their ultrastructural labelling patterns. For both antibodies, labelling was very specific for olfactory cilia; both bound amply to the thick proximal and the thinner and long distal parts of the cilia. Dendritic knobs showed little labelling if any. Dendritic receptor cell structures below the knobs, supporting cell structures, and respiratory cilia did not immunolabel. There were no obvious differences in morphology between labelled and unlabelled receptor cells and their cilia. Labelling could be followed up to a distance of about 15 microns from the knobs along the distal parts of the cilia. When labelled cells were observed, this signal was detectable in two, sometimes three, sections taken through these cells while being consistently absent in neighbouring cells. This pattern argues strongly for the specificity of the labelling. In conclusion, very few receptor cells labelled with the antibodies to putative odour receptors. Additionally the olfactory cilia, the cellular regions that first encounter odour molecules and that are thought to transduce the odorous signal, displayed the most intense labelling with both antibodies. Consequently, the results showed these cilia as having many copies of the putative receptors. Finally, similar patterns of subcellular labelling were displayed in two different species, despite the use of different antibodies. Thus, this study provides compelling evidence that the heptahelical putative odour receptors localize in the olfactory cilia.
针对与大鼠和小鼠不同假定气味受体相对应的合成肽,制备了两种不同的多克隆抗体。通过冷冻固定和免疫金超微结构程序观察到,这两种抗体均能选择性地标记嗅纤毛。检测到标记的嗅觉器官区域与光镜水平下发现的区域一致。免疫阳性细胞很少见;这些受体细胞中只有约0.4%被标记。尽管存在化学、物种和地形差异,但两种抗体在超微结构标记模式上表现相同。对于两种抗体而言,标记对嗅纤毛具有高度特异性;二者都能大量结合纤毛较粗的近端以及较细且长的远端部分。树突状小体即使有标记也很少。小体下方的树突状受体细胞结构、支持细胞结构和呼吸纤毛均未免疫标记。标记和未标记的受体细胞及其纤毛在形态上没有明显差异。沿着纤毛的远端部分,从树突状小体起大约15微米的距离内都能追踪到标记。当观察到标记细胞时,在通过这些细胞的两个,有时是三个切片中可检测到该信号,而相邻细胞中始终没有。这种模式有力地证明了标记的特异性。总之,用假定气味受体抗体标记的受体细胞极少。此外,嗅纤毛作为首先接触气味分子并被认为可转导气味信号的细胞区域,用两种抗体标记时显示出最强的标记。因此,结果表明这些纤毛有许多假定受体的拷贝。最后,尽管使用了不同的抗体,但在两个不同物种中显示出相似的亚细胞标记模式。因此,本研究提供了令人信服的证据,证明七螺旋假定气味受体定位于嗅纤毛中。