Debbage P L, O'Dell D S, Fraser D, James D W
Histochemistry. 1980;68(2):183-95. doi: 10.1007/BF00489513.
We report here the results observed when tubulin fluorescence immunohistochemistry is performed upon dissociated cultures of nervous tissue, principally of chick embryo spinal cord. When fixation includes nonpolar solvents or detergents, a uniform fluorescence is seen in neuron perikarya (with the exception of their nuclei), and the processes to which they give rise. Fixation with formaldehyde or glutaraldehyde alone, however, results in a discontinuous staining of neurites, and a less regular staining of their perikarya. The former pattern of response can be elicited if aldehyde fixation is followed by exposure to non-polar solvents. Such results are obtained both in thinly spread regions of the cultures, where neurons and their processes can easily be seen, and in the cell aggregates that also characterise them. Possible interpretations of these results are discussed.
我们在此报告了对主要来自鸡胚脊髓的神经组织解离培养物进行微管蛋白荧光免疫组织化学检测时所观察到的结果。当固定剂中含有非极性溶剂或去污剂时,在神经元胞体(除细胞核外)及其发出的突起中可见均匀的荧光。然而,单独使用甲醛或戊二醛固定会导致神经突出现间断染色,其胞体染色也不太规则。如果在醛类固定后再用非极性溶剂处理,就能引发前一种反应模式。在培养物的稀薄铺展区域(此处神经元及其突起易于观察)以及同样具有代表性的细胞聚集体中均获得了此类结果。文中讨论了这些结果可能的解释。