Bozdech M J, Bainton D F
J Exp Med. 1981 Jan 1;153(1):182-95. doi: 10.1084/jem.153.1.182.
A reaction for an esterase, with a nonhalogenated, short-chain naphthyl ester (alpha-naphthyl butyrate or alpha-naphthyl acetate) as the substrate, has been used to identify mononuclear phagocytes by light microscopy. By analyzing techniques used in the collection, separation, fixation, processing, and embedding of human blood leukocytes for electron microscopy, we adapted the light microscopic method for use in determining the fine structural localization of this reaction. In monocytes, the reaction product covered the external surface of the plasma membrane. This distribution indicated that monocytic esterase is an ectoenzyme. The addition of NaF completely inhibited the monocytic reaction. In lymphocytes, the reaction product was localized in membrane-bounded intracellular organelles, similar to those previously shown to contain phospholipid and called Gall bodies. These organelles correspond with the punctate densities or focal reaction product observed by light microscopy. Other investigators believe that this distribution of enzyme in lymphocytes marks a subset of T cells, the Tmicro. The lymphocytic reaction was not inhibited by NaF.
以非卤代短链萘酯(α-萘丁酸酯或α-萘乙酸酯)为底物的酯酶反应,已被用于通过光学显微镜鉴定单核吞噬细胞。通过分析用于电子显微镜检查的人血白细胞采集、分离、固定、处理和包埋技术,我们对光学显微镜方法进行了改进,以用于确定该反应的精细结构定位。在单核细胞中,反应产物覆盖质膜的外表面。这种分布表明单核细胞酯酶是一种外切酶。添加氟化钠完全抑制了单核细胞反应。在淋巴细胞中,反应产物定位于膜结合的细胞内细胞器中,类似于先前显示含有磷脂并称为高尔基体的细胞器。这些细胞器与光学显微镜下观察到的点状密度或局灶性反应产物相对应。其他研究者认为,淋巴细胞中这种酶的分布标志着T细胞的一个亚群,即T微小细胞。淋巴细胞反应不受氟化钠抑制。