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DOI 10.1016/s0165-0270(02)00040-7

Медицинская библиотека · Journal of neuroscience methods · 2002

Tracking sodium channels in live cells: confocal imaging using fluorescently labeled toxins.

Massensini Andre R, Suckling John, Brammer Michael J, Moraes-Santos Tasso, Gomez Marcus V, Romano-Silva Marco A

СтатьяПоддержка исследования: вне правительства СШАПеревод в очереди

Аннотация

One particularly important class of ion channels in excitable cells are the voltage-dependent sodium channels (VDSC). Knowledge of the distribution of VDSC in living cells is important for studies of neuronal excitability, development, and plasticity. Here, we demonstrate a new method for visualizing the spatial distribution of VDSC in living cells. To illustrate the capabilities of the technique, the distribution of VDSC in GH3 cells was revealed with fluorescent derivatives of the alpha-type and beta-type scorpion toxins in conjunction with laser scanning confocal microscopy. Cells exhibited fluorescent hot spots on the surface of the membrane. This characteristic staining pattern was prevented by pre-incubation with unlabeled native toxins and blocked by membrane depolarization for alpha-type toxins. Labeling was not observed in cells lacking sodium channels (HEK 293) after incubation with fluorescent-labeled toxins. Image processing techniques were applied to identify the location of each cluster of labeled VDSC in these cells. The proposed method eliminates artefacts commonly introduced during sample preparation for immunostaining and should prove to be a valuable research tool for investigating VDSC distribution in living specimens.

Для цитирования: Massensini Andre R, Suckling John, Brammer Michael J, Moraes-Santos Tasso, Gomez Marcus V, Romano-Silva Marco A. Tracking sodium channels in live cells: confocal imaging using fluorescently labeled toxins.. Journal of neuroscience methods. 2002. DOI: 10.1016/s0165-0270(02)00040-7.

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