Boer G J, Nolten J W, Koenders Y, van Rheenen-Verberg C M
Brain Res. 1976 Sep 17;114(2):257-77. doi: 10.1016/0006-8993(76)90670-3.
A microcellular dispersion procedure for the rat neurohypophysis was developed, comprising tissue softening and dissociation using a special sieving sytringe. In preparatory studies the influence of mesh width, and treatment with trypsin, pronase or collagenase-hyaluronidase was investigated using light and electron microscopy, as well as with microchemistry by means of protein and lactate dehydrogenase activity determinations. Trypsinization gave the best results. In the final adopted procedure, 3 incubated neurohypophyses were sequentially sieved through a 200- and a 50-mum mesh. The resulting 50-mul dispersion was found to contain numerous ultrastructurally well-preserved pinched-off axonal endings (neurosecretosomes), and pituicytes often revealing processes. On the basis of DNA and oxytocin assays 11% of the pituicytes and 28% of the axonal cytoplasm were recovered. Oxytocin immunofluorescence microscopy showed hormone within the neurosecretosomes, but often also in the cytoplasm of pituicytes. Microdensity gradient centrifugation was performed on neurohypophyseal disperions, in order to obtain fractions enriched for neurosecretosomes and pituicytes. Fractions were characterized by means of phase contrast, oxytocin immunofluorescence and electron microscopy, as well as by oxytocin and DNA assays as respective markers. With a 10:14:22% (w/v) Ficoll gradient, fractions were obtained for which the relative purification was by a factor of 4 on the basis of DNA/oxytocin ratios.
已开发出一种用于大鼠神经垂体的微细胞分散程序,该程序包括使用特殊的筛网注射器进行组织软化和解离。在前期研究中,通过光学显微镜和电子显微镜,以及通过蛋白质和乳酸脱氢酶活性测定的微量化学方法,研究了筛网宽度以及用胰蛋白酶、链霉蛋白酶或胶原酶 - 透明质酸酶处理的影响。胰蛋白酶消化产生了最佳结果。在最终采用的程序中,将3个孵育过的神经垂体依次通过200微米和50微米的筛网进行筛选。发现所得的50微升分散液含有大量超微结构保存良好的缩窄轴突末梢(神经分泌小体),以及经常显示出突起的垂体细胞。基于DNA和催产素测定,回收了11%的垂体细胞和28%的轴突细胞质。催产素免疫荧光显微镜检查显示神经分泌小体内有激素,但在垂体细胞的细胞质中也经常有。对神经垂体分散液进行了微量密度梯度离心,以获得富含神经分泌小体和垂体细胞的组分。通过相差显微镜、催产素免疫荧光和电子显微镜,以及分别以催产素和DNA测定作为标记来对各组分进行表征。使用10:14:22%(w/v)的菲可梯度,获得了基于DNA/催产素比率相对纯化因子为4的组分。