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Optical estimation of absolute membrane potential using fluorescence lifetime imaging.

Julia R Lazzari-Dean | Anneliese Mm Gest | Evan W Miller
eLife | 2019

All cells maintain ionic gradients across their plasma membranes, producing transmembrane potentials (Vmem). Mounting evidence suggests a relationship between resting Vmem and the physiology of non-excitable cells with implications in diverse areas, including cancer, cellular differentiation, and body patterning. A lack of non-invasive methods to record absolute Vmem limits our understanding of this fundamental signal. To address this need, we developed a fluorescence lifetime-based approach (VF-FLIM) to visualize and optically quantify Vmem with single-cell resolution in mammalian cell culture. Using VF-FLIM, we report Vmem distributions over thousands of cells, a 100-fold improvement relative to electrophysiological approaches. In human carcinoma cells, we visualize the voltage response to growth factor stimulation, stably recording a 10-15 mV hyperpolarization over minutes. Using pharmacological inhibitors, we identify the source of the hyperpolarization as the Ca2+-activated K+ channel KCa3.1. The ability to optically quantify absolute Vmem with cellular resolution will allow a re-examination of its signaling roles.

Pubmed ID: 31545164

Associated grants

  • Agency: National Science Foundation, International
    Id: GRFP
  • Agency: March of Dimes Foundation, International
    Id: 5-FY-16-65
  • Agency: Alfred P. Sloan Foundation, International
    Id: FG-2016-6359
  • Agency: NIH HHS, United States
    Id: R35GM119855
  • Agency: NIGMS NIH HHS, United States
    Id: R35 GM119855

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