Lipsky N G, Pagano R E
Science. 1985 May 10;228(4700):745-7. doi: 10.1126/science.2581316.
The Golgi complex, a membranous organelle with important functions in membrane traffic and macromolecular synthesis, has been stained in living cells with a fluorescent sphingolipid. Cells were first incubated with liposomes containing N-[7-(4-nitrobenzo-2-oxa-1,3-diazole)]-6-aminocaproyl sphingosine (C6-NBD-ceramide), or with a bovine serum albumin complex of the fluorescent lipid, and then examined by fluorescence microscopy. An intensely fluorescent perinuclear structure was identified as the Golgi apparatus by its colocalization with known Golgi markers in fixed cells. C6-NBD-ceramide was used to observe the morphology of the Golgi apparatus in living cells in the presence or absence of monensin or Colcemid, and during mitosis. In all cases, C6-NBD-ceramide revealed a Golgi apparatus in the living cell that was identical to that obtained with conventional procedures that require fixation.
高尔基体是一种在膜运输和大分子合成中具有重要功能的膜性细胞器,已用荧光鞘脂对活细胞进行了染色。细胞首先与含有N-[7-(4-硝基苯并-2-恶唑-1,3-二氮杂环戊二烯)]-6-氨基己酰鞘氨醇(C6-NBD-神经酰胺)的脂质体一起孵育,或与荧光脂质的牛血清白蛋白复合物一起孵育,然后通过荧光显微镜检查。通过与固定细胞中已知的高尔基体标记物共定位,一个强烈荧光的核周结构被鉴定为高尔基体。C6-NBD-神经酰胺用于观察在有或没有莫能菌素或秋水仙酰胺的情况下以及在有丝分裂期间活细胞中高尔基体的形态。在所有情况下,C6-NBD-神经酰胺在活细胞中显示出的高尔基体与通过需要固定的传统方法获得的高尔基体相同。