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[用新型吖啶染料对活的海拉细胞和LM细胞中的线粒体进行荧光染色(作者译)]

[The fluorescent staining of mitochondria in living HeLa- and LM-cells with new acridine dyes (author's transl)].

作者信息

Erbrich U, Naujok A, Petschel K, Zimmermann H W

出版信息

Histochemistry. 1982;74(1):1-7. doi: 10.1007/BF00495046.

DOI:10.1007/BF00495046
PMID:7085344
Abstract

The fluorescent staining of mitochondria in living cells with new acridine dyes is reported. The fluorescent dyes used are derivatives of acridine orange (AO) and of 3-amino-6-methoxyacridine (AMA) with various residues in 9- or 10-position (Scheme 1). They are either permanent cationic dyes or cations which are formed by protonation in the culture medium. HeLa cells and mouse fibroblasts (LM cells) have been used for our staining experiments. On favourable conditions we succeeded in staining the mitochondria not only orthochromatically but also metachromatically. Photodynamical effects which have been observed during the exposure of the stained cells in the fluorescence microscope are described. The residues in 9- or 10-position favour the dye accumulation in the mitochondria. Vital staining with the basic compounds AO and AMA however leads to the formation of metachromatically stained lysosomes in the orthochromatically stained cytoplasm. The dye 3-amino-6-methoxy-9-(2-hydroxyethyl)acridine stains the nucleus of living cells.

摘要

报道了用新型吖啶染料对活细胞中线粒体进行荧光染色的情况。所用的荧光染料是吖啶橙(AO)和3-氨基-6-甲氧基吖啶(AMA)的衍生物,在9位或10位带有各种取代基(方案1)。它们要么是永久性阳离子染料,要么是在培养基中通过质子化形成的阳离子。我们使用了HeLa细胞和小鼠成纤维细胞(LM细胞)进行染色实验。在有利条件下,我们成功地不仅以正色方式而且以异染方式对线粒体进行了染色。描述了在荧光显微镜下对染色细胞进行照射期间观察到的光动力效应。9位或10位的取代基有利于染料在线粒体中的积累。然而,用碱性化合物AO和AMA进行活体染色会导致在正色染色的细胞质中形成异染染色的溶酶体。染料3-氨基-6-甲氧基-9-(2-羟乙基)吖啶可对活细胞的细胞核进行染色。

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[The fluorescent staining of mitochondria in living HeLa- and LM-cells with new acridine dyes (author's transl)].[用新型吖啶染料对活的海拉细胞和LM细胞中的线粒体进行荧光染色(作者译)]
Histochemistry. 1982;74(1):1-7. doi: 10.1007/BF00495046.
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Histochemistry. 1993 Jan;99(1):75-83. doi: 10.1007/BF00268024.
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[Fluorescent staining of chromosomes and nuclear structures in living LM- and HeLa-cells with new acridine dyes].[利用新型吖啶染料对活的LM细胞和HeLa细胞中的染色体及核结构进行荧光染色]
Histochemistry. 1982;76(2):219-28. doi: 10.1007/BF00501924.
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[Effect of acridine dyes on the ultrastructure of mitochondria in HeLa and LM cells].[吖啶染料对HeLa细胞和LM细胞线粒体超微结构的影响]
Histochemistry. 1982;76(2):211-8. doi: 10.1007/BF00501923.
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[Hydrophobic acridine dyes for fluorescence staining of mitochondria in living cells. 2. Comparison of staining of living and fixed Hela-cells with NAO and DPPAO].[用于活细胞中线粒体荧光染色的疏水性吖啶染料。2. 用NAO和DPPAO对活的和固定的Hela细胞进行染色的比较]
Histochemistry. 1984;80(4):385-8. doi: 10.1007/BF00495422.
9
[Hydrophobic acridine dyes for fluorescence staining of mitochondria in living cells. 1. Thermodynamic and spectroscopic properties of 10-n-alkylacridine orange chlorides].用于活细胞中线粒体荧光染色的疏水性吖啶染料。1. 10 - n - 烷基吖啶橙氯化物的热力学和光谱性质
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10
[Hydrophobic acridine dyes for fluorescent staining of mitochondria in living cells. 3. Specific accumulation of the fluorescent dye NAO on the mitochondrial membranes in HeLa cells by hydrophobic interaction. Depression of respiratory activity, changes in the ultrastructure of mitochondria due to NAO. Increase of fluorescence in vital stained mitochondria in situ by irradiation].[用于活细胞中线粒体荧光染色的疏水性吖啶染料。3. 荧光染料NAO通过疏水相互作用在HeLa细胞线粒体膜上的特异性积累。NAO对呼吸活性的抑制,线粒体超微结构的变化。通过照射使原位活体染色线粒体中的荧光增强]
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