Castejón O J, Apkarian R P
Institute of Biological Researches, Faculty of Medicine, University of Zulia, Maracaibo, Venezuela.
J Submicrosc Cytol Pathol. 1992 Oct;24(4):549-62.
This paper provides an exploration into the inner and outer surfaces of vertebrate cerebellar neurons utilizing secondary electron (SE-I and SE-II) topographic contrasts. SE-I enriched chromium coated, cryofractured Rhesus monkey cerebellum staged within the condenser/objective stage of SEMs equipped with high brightness LaB6 and field emission emitters generated quality images of intact and fractured nerve cells studied at intermediate and high magnifications. These images were compared with conventional SE-III images of gold-palladium teleost fish cerebellar neurons and transmission electron micrographs of mouse cerebellar nerve cells obtained either by thin-sections or freeze-etch replicas. Chromium coated Rhesus monkey granule and Golgi cell surfaces revealed smooth, accurately delineated profiles of true cell surface features, which lacked the SE-III dominated brilliance of conventional teleost fish gold or gold-palladium, decorated neurons. Chromium coated fractured nerve processes showed the outer smooth surface of interconnected anastomotic networks or ER tubules, vesicles and cisterns. Cross fractured presynaptic endings of parallel fibers in the molecular layer exhibited spheroidal synaptic vesicles and SE-I edge brightness contrast delineated their limiting plasma membranes. Fractured synaptic endings showed a homogeneous extravesicular material surrounding the synaptic vesicles. The presynaptic dense projections appeared as columnar shaped structures. The postsynaptic membrane and associated postsynaptic density showed a discontinuous surface formed by round subunits 25-35 nm in diameter. The neuroglial cytoplasm ensheathing nerve process exhibited a smooth discontinuous surface. The surface of the myelin sheath showed a mixed population of globular structures 10-30 nm in diameter, apparently corresponding, according to freeze-etch images, to protein and phospholipid microdomains.
本文利用二次电子(SE-I和SE-II)形貌对比,对脊椎动物小脑神经元的内表面和外表面进行了探索。在配备高亮度LaB6和场发射源的扫描电子显微镜的聚光镜/物镜台上,对富集SE-I的经铬涂层处理的恒河猴小脑冷冻断裂样本进行观察,在中高放大倍数下生成了完整和断裂神经细胞的高质量图像。这些图像与硬骨鱼小脑神经元的传统SE-III图像以及通过薄切片或冷冻蚀刻复制品获得的小鼠小脑神经细胞的透射电子显微照片进行了比较。经铬涂层处理的恒河猴颗粒细胞和高尔基细胞表面显示出光滑、精确勾勒的真实细胞表面特征轮廓,缺乏传统硬骨鱼金或金钯修饰神经元中以SE-III为主的亮度。经铬涂层处理的断裂神经突起显示出相互连接的吻合网络或内质网管、囊泡和平行池的外表面光滑。分子层中平行纤维的交叉断裂突触前末梢呈现出球形突触囊泡,SE-I边缘亮度对比勾勒出它们的限制质膜。断裂的突触末梢显示突触囊泡周围有均匀的囊泡外物质。突触前致密突起呈现为柱状结构。突触后膜和相关的突触后致密物质显示出由直径25 - 35nm的圆形亚基形成的不连续表面。包裹神经突起的神经胶质细胞质呈现出光滑的不连续表面。髓鞘表面显示出直径为10 - 30nm的球状结构混合群体,根据冷冻蚀刻图像,这些结构显然对应于蛋白质和磷脂微区。