scholarly journals A membrane-activatable near-infrared fluorescent probe with ultra-photostability for mitochondrial membrane potentials

The Analyst ◽  
2016 ◽  
Vol 141 (12) ◽  
pp. 3679-3685 ◽  
Author(s):  
Wei Ren ◽  
Ao Ji ◽  
Omran Karmach ◽  
David G. Carter ◽  
Manuela M. Martins-Green ◽  
...  
Keyword(s):  
Membrane Potential ◽  
Fluorescent Probe ◽  
Mitochondrial Membrane Potential ◽  
Mitochondrial Membrane ◽  
Near Infrared ◽  
Living Cells ◽  
Membrane Potentials ◽  
Fluorescence Quencher

Dark for light: A fluorescence quencher was turned into a near-infrared probe for mitochondrial membrane potential in living cells and mice.

Fabrication of a fluorescent probe for reversibly monitoring mitochondrial membrane potential in living cells

2021 ◽  
Vol 13 (14) ◽  
pp. 1715-1719
Author(s):  
Dingyi Guo ◽  
Jie Sun ◽  
Minggang Tian ◽  
Weiying Lin
Keyword(s):  
Reactive Oxygen Species ◽  
Membrane Potential ◽  
Fluorescent Probe ◽  
Mitochondrial Membrane Potential ◽  
Mitochondrial Membrane ◽  
Cell Damage ◽  
Reactive Oxygen ◽  
Living Cells ◽  
Oxygen Species

A fluorescent probe for reversibly monitoring mitochondrial membrane potential in living cells has been constructed successfully, which could be employed to visualize cell damage by reactive oxygen species.

scholarly journals Near infrared light exposure is associated with increased mitochondrial membrane potential in retinal pigmented epithelial cells

2020 ◽  
Vol 19 (10) ◽  
pp. 1455-1459
Author(s):  
Catherine Rono ◽  
Tiffany R Oliver
Keyword(s):  
Membrane Potential ◽  
Epithelial Cells ◽  
Mitochondrial Membrane Potential ◽  
Mitochondrial Membrane ◽  
Near Infrared ◽  
Light Exposure ◽  
Infrared Light ◽  
Near Infrared Light ◽  
Retinal Pigmented Epithelial Cells

The goal of this study was to characterize the effect of near-infrared light exposure on mitochondrial membrane potential, in vitro.

scholarly journals Development of a High Throughput Screening Assay for Mitochondrial Membrane Potential in Living Cells

2002 ◽  
Vol 7 (4) ◽  
pp. 383-389 ◽  
Author(s):  
Shu-Gui Huang
Keyword(s):  
Membrane Potential ◽  
Mitochondrial Membrane Potential ◽  
High Throughput ◽  
High Throughput Screening ◽  
Mitochondrial Membrane ◽  
Living Cells ◽  
Screening Assay ◽  
Mitochondrial Inner Membrane ◽  
Obesity And Diabetes ◽  
High Throughput Screening Assay

The mitochondrion plays a pivotal role in energy metabolism in eukaryotic cells. The electrochemical potential across the mitochondrial inner membrane is regulated to cope with cellular energy needs and thus reflects the bioenergetic state of the cell. Traditional assays for mitochondrial membrane potential are not amenable to high-throughput drug screening. In this paper, I describe a high-throughput assay that measures the mitochondrial membrane potential of living cells in 96- or 384-well plates. Cells were first treated with test compounds and then with a fluorescent potentiometric probe, the cationic-lipophilic dye tetramethylrhodamine methyl ester (TMRM). The cells were then washed to remove free compounds and probe. The amount of TMRM retained in the mitochondria, which is proportional to the mitochondrial membrane potential, was measured on an LJL Analyst fluorescence reader. Under optimal conditions, the assay measured only the mitochondrial membrane potential. The chemical uncouplers carbonylcyanide m-chlorophenyl hydrazone and dinitrophenol decreased fluorescence intensity, with IC50 values (concentration at 50% inhibition) similar to those reported in the literature. A Z' factor of greater than 0.5 suggests that this cell-based assay can be adapted for high-throughput screening of chemical libraries. This assay may be used in screens for drugs to treat metabolic disorders such as obesity and diabetes, as well as cancer and neurodegenerative diseases.

scholarly journals Energy transduction in intact synaptosomes. Influence of plasma-membrane depolarization on the respiration and membrane potential of internal mitochondria determined in situ

1980 ◽  
Vol 186 (1) ◽  
pp. 21-33 ◽  
Author(s):  
I D Scott ◽  
D G Nicholls
Keyword(s):  
Plasma Membrane ◽  
Membrane Potential ◽  
Mitochondrial Membrane Potential ◽  
Mitochondrial Membrane ◽  
Significant Proportion ◽  
Membrane Potentials ◽  
Simultaneous Estimation ◽  
Anaerobic Glycolysis ◽  
Mitochondrial Potential ◽  
Plasma Membrane Potential

A method is described, based on the differential accumulation of Rb+ and methyltriphenylphosphonium, for the simultaneous estimation of the membrane potentials across the plasma membrane of isolated nerve endings (synaptosomes), and across the inner membrane of mitochondria within the synaptosomal cytoplasm. These determinations, together with measurements of respiratory rates, and ATP and phosphocreatine concentrations, are used to define the bioenergetic behaviour of isolated synaptosomes under a variety of conditions. Under control conditions, in the presence of glucose, the plasma and mitochondrial membrane potentials are respectively 45 and 148mV. Addition of a proton translocator induces a 5-fold increase in respiration, and abolishes the mitochondrial membrane potential. The addition of rotenone to inhibit respiration does not affect the plasma membrane potential, and only lowers the mitochondrial membrane potential to 128mV. Evidence is presented that ATP synthesis by anaerobic glycolysis is sufficient under these conditions to maintain ATP-dependent processes, including the reversal of the mitochondrial ATP synthetase. Addition of oligomycin under non-respiring conditions leads to a complete collapse of the mitochondrial potential. Even under control conditions the plasma membrane (Na+ + K+)-dependent ATPase is responsible for a significant proportion of the synaptosomal ATP turnover. Veratridine greatly increases respiration, and depolarizes the plasma membrane, but only slightly lowers the mitochondrial membrane potential. High K+ and ouabain also lower the plasma membrane potential without decreasing the mitochondrial membrane potential. In non-respiring synaptosomes, anaerobic glycolysis is incapable of maintaining cytosolic ATP during the increased turnover induced by veratridine, and the mitochondrial membrane potential collapses. It is concluded that the internal mitochondria must be considered in any study of synaptosomal transport.

Mitochondrial membrane potential regulation is independent of c-fos expression

1999 ◽  
Vol 77 (3) ◽  
pp. 195-203
Author(s):  
Roger A Moorehead ◽  
Gurmit Singh
Keyword(s):  
Membrane Potential ◽  
Ovarian Carcinoma ◽  
Mitochondrial Membrane Potential ◽  
Mitochondrial Membrane ◽  
Membrane Potentials ◽  
Rhodamine 123 ◽  
Parental Line ◽  
Rat Fibroblasts ◽  
Human Ovarian Carcinoma ◽  
Fos Expression

Tumour cells contain mitochondria with elevated membrane potentials compared with normal cells, and thus this feature provides a selective target for destroying tumour cells. To improve mitochondrial-based therapies, a better understanding of the factors involved in regulating mitochondria are required. Since v-fos overexpression has been shown to elevate mitochondrial membrane potentials in rat fibroblasts, we investigated whether the human homologue, c-fos, was also capable of regulating the mitochondrial membrane potential in cells. Rat fibroblasts transfected with the c-fos gene did not accumulate more rhodamine 123 (Rh123) nor did they retain this Rh123 for extended periods of time compared with their parental line. Moreover, there was no difference in survival following dequalinium chloride (Deca) treatment between transfectants and controls. Similarly, reduction of c-fos expression in rat fibroblasts did not significantly alter their mitochondrial membrane potential. In addition, human ovarian carcinoma cells, which overexpress the c-fos gene, did not accumulate more Rh123 nor were they hypersensitive to Deca compared with their parental line. In another human ovarian carcinoma cell line, selection of variants with lower mitochondrial membrane potential did not alter c-fos mRNA or protein levels. These data suggest that alterations in c-fos expression do not regulate the magnitude of the mitochondrial membrane potential.Key words: c-fos, mitochondria, membrane potential, rhodamine 123 (Rh123), lipophilic cations.

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