Rusakov D A, Podini P, Villa A, Meldolesi J
Bogomoletz Institute of Physiology, Academy of Science, Kiev, Ukraine.
J Neurocytol. 1993 Apr;22(4):273-82. doi: 10.1007/BF01187126.
Stacks of regularly spaced, flat, smooth-surfaced endoplasmic reticulum cisternae frequently observed in both the cell body and dendrites of cerebellar Purkinje neurons, were previously shown by immunocytochemistry to be highly enriched in receptors for the second messenger, inositol 1,4,5-trisphosphate. Morphometric analyses have been carried out on randomly selected thin section images of rat Purkinje neurons to reveal the tridimensional organization of these structures. Individual stacked cisternae (on the average approximately 3.5 per stack) were shown to be separated from each other by a 23.5 nm space occupied by perpendicular bridges, approximately 20 nm in diameter, most probably composed by two apposed receptor homotetramer molecules, inserted into the parallel membranes in their hydrophobic domains. In the stacked membranes the density of the bridges was approximately 500 microns -2, corresponding to approximately 15% of the surface area. The lateral distribution of bridges was not random, but revealed regular distances that might correspond to unoccupied receptor slots. In each stack, the external cisternae were often in direct lumenal continuity with conventional elements of the endoplasmic reticulum, whereas the internal cisternae were not. Since continuities between stacked cisternae were never observed, the results indicate that the internal cisternae are at least transitorily discrete, i.e. they are not in permanent lumenal continuity with the rest of the endoplasmic reticulum. To our knowledge this is the first demonstration of a physical subcompartmentalization of the latter endomembrane system in a non-mitotic cells. A model for the biogenesis of cisternal stacks, based on the head-to-head binding and lateral interaction of the inositol 1,4,5-trisphosphate receptor molecules in the plane of the interacting membranes, is proposed and critically discussed.
在小脑浦肯野神经元的细胞体和树突中经常观察到成排的、间隔规则、表面平滑的内质网池。免疫细胞化学先前已表明,这些内质网池中高度富集了第二信使肌醇1,4,5 -三磷酸的受体。已对随机选择的大鼠浦肯野神经元薄切片图像进行形态计量分析,以揭示这些结构的三维组织。单个堆叠的内质网池(平均每堆叠约3.5个)被证明彼此之间由一个23.5纳米的空间隔开,该空间被垂直桥占据,直径约20纳米,很可能由两个并列的受体同四聚体分子组成,它们在其疏水结构域插入平行膜中。在堆叠的膜中,桥的密度约为500微米-2,约占表面积的15%。桥的横向分布不是随机的,而是显示出可能对应于未占据受体槽的规则间距。在每个堆叠中,外部的内质网池通常与内质网的常规成分直接在管腔上连续,而内部的内质网池则不然。由于从未观察到堆叠的内质网池之间有连续性,结果表明内部的内质网池至少在暂时是离散的,即它们与内质网的其余部分没有永久的管腔连续性。据我们所知,这是首次在非有丝分裂细胞中证明后者内膜系统的物理亚区室化。基于肌醇1,4,5 -三磷酸受体分子在相互作用膜平面上的头对头结合和横向相互作用,提出并批判性地讨论了内质网池堆叠生物发生的模型。