Real-Time Detection of Neuronal Cell Death by Impedance-Based Analysis using the xCELLigence System
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Time course analyses of neuronal cell death and its underlying mechanisms require laborious experiments and multiple endpoint assays, often involving labelling with irritating compounds and cell disruption. A recent study used the xCELLigence System of Roche to investigate the response of the neuronal-like cell line HT-22 and cultured primary rat cortical neurons to different cell death stimuli and neuroprotectants.
The xCELLigence System provides a non-invasive and label-free way to continuously monitor cellular parameters such as viability, death, adhesion, and proliferation. It records electrical impedance of cells grown on microelectrode arrays integrated into the bottom of each well of an E-Plate 96. Cell-sensor impedance is expressed as the Cell Index (CI), changes in the CI correlate to modifications in cell morphology.
In the study, xCELLigence System’s recording of CI values allowed monitoring of primary cortical neuronal culture conditions, including plating, removal of glial cells, compound administration and cell death profiling. In addition, the system clearly revealed neurotoxic and neuroprotective effects in real-time. The system adds significant information to data gained from conventional endpoint assays, identifying optimal time points for performing such assays.
Following an initial rise in impedance HT-22 cells displayed a constant growth rate over time with absolute CI values proportional to the initial seeding density, caused by adherence of the cells to the bottom of the well. After treatment with glutamate, CI values began to decrease rapidly, correlating with dose-dependent glutamate-induced cell death, which was in turn confirmed by the results of MTT viability assays, as well as being consistent with the kinetics of cell death reported in mitochondrial fragmentation and AIF nuclear translocation assays.
In the next step of the experiment, BI-6C9 (an inhibitor of the pro-apoptotic BH-3 protein BID) was used to prevent glutamate toxicity in HT-22 cells. BI-6C9-mediated neuroprotection was reflected in the xCELLigence System by a continued rise in CI values, demonstrating that the compound preserved cell morphology and cell survival.
As with HT-22 cells, primary rat cortical neurons showed at first an increase in CI values due to initial cellular attachment to the bottom of the well. Subsequent removal of proliferating glial cells with cytosine-arabinofuranoside caused an expected slight decrease in CI values. To monitor cell death, the primary neuronal cultures were treated with ionomycin or glutamate.
Treatment with ionomycin caused a marked drop in CI correlating with the formation of pyknotic, rounded cell bodies. By comparison, cell death induced by glutamate was significantly delayed, and was reflected by a steady decline in CI values within 48 to 72 hours of treatment. These different cell death effects reflect the delayed activation of cell death signalling by glutamate compared to the more rapid loss of cell membrane integrity and necrotic cell death following ionomycin treatment.
The xCELLigence System provides a non-invasive and label-free way to continuously monitor cellular parameters such as viability, death, adhesion, and proliferation. It records electrical impedance of cells grown on microelectrode arrays integrated into the bottom of each well of an E-Plate 96. Cell-sensor impedance is expressed as the Cell Index (CI), changes in the CI correlate to modifications in cell morphology.
In the study, xCELLigence System’s recording of CI values allowed monitoring of primary cortical neuronal culture conditions, including plating, removal of glial cells, compound administration and cell death profiling. In addition, the system clearly revealed neurotoxic and neuroprotective effects in real-time. The system adds significant information to data gained from conventional endpoint assays, identifying optimal time points for performing such assays.
Following an initial rise in impedance HT-22 cells displayed a constant growth rate over time with absolute CI values proportional to the initial seeding density, caused by adherence of the cells to the bottom of the well. After treatment with glutamate, CI values began to decrease rapidly, correlating with dose-dependent glutamate-induced cell death, which was in turn confirmed by the results of MTT viability assays, as well as being consistent with the kinetics of cell death reported in mitochondrial fragmentation and AIF nuclear translocation assays.
In the next step of the experiment, BI-6C9 (an inhibitor of the pro-apoptotic BH-3 protein BID) was used to prevent glutamate toxicity in HT-22 cells. BI-6C9-mediated neuroprotection was reflected in the xCELLigence System by a continued rise in CI values, demonstrating that the compound preserved cell morphology and cell survival.
As with HT-22 cells, primary rat cortical neurons showed at first an increase in CI values due to initial cellular attachment to the bottom of the well. Subsequent removal of proliferating glial cells with cytosine-arabinofuranoside caused an expected slight decrease in CI values. To monitor cell death, the primary neuronal cultures were treated with ionomycin or glutamate.
Treatment with ionomycin caused a marked drop in CI correlating with the formation of pyknotic, rounded cell bodies. By comparison, cell death induced by glutamate was significantly delayed, and was reflected by a steady decline in CI values within 48 to 72 hours of treatment. These different cell death effects reflect the delayed activation of cell death signalling by glutamate compared to the more rapid loss of cell membrane integrity and necrotic cell death following ionomycin treatment.
