Martone M E, Pollock J A, Jones Y Z, Ellisman M H
National Center for Microscopy and Imaging Research at San Diego, Department of Neurosciences, University of California San Diego, 92093-0608, USA.
J Neurosci. 1996 Dec 1;16(23):7437-46. doi: 10.1523/JNEUROSCI.16-23-07437.1996.
An ultrastructural examination of mRNA within adult rat CA1 hippocampal dendrites was conducted using two different methods. The messages for the alpha and beta forms of the calcium-calmodulin-dependent protein kinase II were localized in ultracryosections using silver-intensified gold detection of isoform-specific oligonucleotide probes. Labeling for both isoforms was observed within the cell bodies and proximal dendrites of pyramidal neurons, but only the alpha form was observed in more distal dendrites. Unfortunately, the morphological preservation of the tissue was not sufficient to determine the localization of labeling relative to subcellular features such as dendritic spines. To address this issue, a preembedding peroxidase-based method was developed, resulting in better preservation of the neuropil. The total population of polyadenylated [poly(A)] mRNA was localized in hippocampus using a biotinylated poly(dT) probe. Poly(A) mRNA was present in the nucleus and throughout the cell body of all hippocampal cells and within isolated dendrites and glial processes within the neuropil. Within pyramidal neurons, labeling was distributed in a longitudinal pattern in proximal apical dendrites. More distally, the amount of labeling diminished, and smaller foci of labeling were observed, particularly near the plasma membrane. Concentrated labeling was present at the base of dendritic spines and, less frequently, near synapses onto the dendritic shaft. These results suggest that dendritic mRNA is found in the vicinity of postsynaptic sites and provide additional evidence that local protein synthesis may play an important role in establishing and maintaining synaptic specializations.
利用两种不同方法对成年大鼠海马CA1区树突内的mRNA进行了超微结构检查。使用银增强金检测同工型特异性寡核苷酸探针,在超低温切片中定位钙调蛋白依赖性蛋白激酶II的α和β两种形式的信息。在锥体神经元的细胞体和近端树突中观察到两种同工型的标记,但仅在更远端的树突中观察到α形式。不幸的是,组织的形态保存不足以确定标记相对于树突棘等亚细胞特征的定位。为了解决这个问题,开发了一种基于预包埋过氧化物酶的方法,从而更好地保存了神经纤维网。使用生物素化的聚(dT)探针在海马中定位多聚腺苷酸化[poly(A)]mRNA的总体。Poly(A)mRNA存在于所有海马细胞的细胞核和整个细胞体中,以及神经纤维网内的孤立树突和胶质细胞突起中。在锥体神经元内,标记在近端顶端树突中呈纵向分布。在更远端,标记量减少,观察到较小的标记灶,特别是靠近质膜处。集中标记出现在树突棘的基部,较少出现在树突轴上的突触附近。这些结果表明,树突mRNA存在于突触后位点附近,并提供了额外的证据,表明局部蛋白质合成可能在建立和维持突触特化中起重要作用。