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Staining of viable and nonviable myotubes and of myofibrils by the fluorescent dye merocyanine 540.

作者信息

Falke J, Lazarides E

出版信息

Differentiation. 1980;17(3):199-204. doi: 10.1111/j.1432-0436.1980.tb01097.x.

DOI:10.1111/j.1432-0436.1980.tb01097.x
PMID:6161052
Abstract

Merocyanine 540 (MC 540) has been reported to interact specifically with excitable plasma membranes in live cells [3]. Here we show that the MC 540 fluorescence staining pattern previously believed to be characteristic of viable myotubes [3] is observed in formaldehyde-fixed cells. In contrast, viable myotubes show an MC 540 fluorescence staining pattern that is characteristic of cell surface staining (no internal structures fluoresce). The specific I-band and H-zone fluorescence of isolated myofibrils is also consistent with the interpretation that the fluorescence patterns previously reported for viable myotubes are in fact characteristic of cells with disrupted plasma membranes. Time-course observations of MC 540 and trypan blue staining of myotubes suggest that when plasma membrane integrity is lost, MC 540 fluorescence can be visualized inside the cell 5-10 min before trypan blue absorbance. Thus the trypan blue viability assay can be misleading when applied to myotubes.

摘要

相似文献

1
Staining of viable and nonviable myotubes and of myofibrils by the fluorescent dye merocyanine 540.
Differentiation. 1980;17(3):199-204. doi: 10.1111/j.1432-0436.1980.tb01097.x.
2
Merocyanine 540 as a fluorescent probe of membranes: staining of electrically excitable cells.部花青540作为膜的荧光探针:可电兴奋细胞的染色
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Myofibrillogenesis in living cells microinjected with fluorescently labeled alpha-actinin.在注射了荧光标记α-辅肌动蛋白的活细胞中的肌原纤维生成。
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7
Electrostatic interaction between merocyanine 540 and liposomal and mitochondrial membranes.部花青540与脂质体膜和线粒体膜之间的静电相互作用。
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A permanent cell viability assay using alcian blue.使用阿尔新蓝的永久性细胞活力测定法。
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