Kiebler M A, López-García J C, Leopold P L
EMBL, Cell Biology Programme, Heidelberg, Germany.
FEBS Lett. 1999 Feb 19;445(1):80-6. doi: 10.1016/s0014-5793(99)00077-0.
We report a revised and improved isolation procedure for CA3-dendritic spines, most of them still in association with mossy fiber terminals resulting in a 7.5-fold enrichment over nuclei and a 29-fold enrichment over myelin. Additionally, red blood cells, medullated fibers, mitochondria and small synaptosomes were significantly depleted. We show by high resolution electron microscopy that this subcellular fraction contains numerous dendritic spines with a rich ultrastructure, e.g. an intact spine apparatus, membranous organelles, free and membrane-bound polyribosomes, endocytic structures and mitochondria. This improved experimental system will allow us to study aspects of post-synaptic functions at the biochemical and molecular level.
我们报告了一种经过修订和改进的CA3树突棘分离程序,其中大多数树突棘仍与苔藓纤维终末相关联,相对于细胞核实现了7.5倍的富集,相对于髓磷脂实现了29倍的富集。此外,红细胞、有髓纤维、线粒体和小突触体显著减少。我们通过高分辨率电子显微镜显示,该亚细胞组分包含众多具有丰富超微结构的树突棘,例如完整的棘器、膜性细胞器、游离和膜结合的多聚核糖体、内吞结构和线粒体。这个改进的实验系统将使我们能够在生化和分子水平上研究突触后功能的各个方面。