Alpha Hemolysin Induces an Increase of Erythrocytes Calcium: A FLIM 2-Photon Phasor Analysis Approach
نویسندگان
چکیده
α-Hemolysin (HlyA) from Escherichia coli is considered as the prototype of a family of toxins called RTX (repeat in toxin), a group of proteins that share genetic and structural features. HlyA is an important virulence factor in E. coli extraintestinal infections, such as meningitis, septicemia and urinary infections. High concentrations of the toxin cause the lysis of several cells such as erythrocytes, granulocytes, monocytes, endothelial and renal epithelial cells of different species. At low concentrations it induces the production of cytokines and apoptosis. Since many of the subcytolytic effects in other cells have been reported to be triggered by the increase of intracellular calcium, we followed the calcium concentration inside the erythrocytes while incubating with sublytic concentrations of HlyA. Calcium concentration was monitored using the calcium indicator Green 1, 2-photon excitation, and fluorescence lifetime imaging microscopy (FLIM). Data were analyzed using the phasor representation. In this report, we present evidence that, at sublytic concentrations, HlyA induces an increase of calcium concentration in rabbit erythrocytes in the first 10 s. Results are discussed in relation to the difficulties of measuring calcium concentrations in erythrocytes where hemoglobin is present, the contribution of the background and the heterogeneity of the response observed in individual cells.
منابع مشابه
Hardware-friendly bi-exponential fluorescence lifetime imaging algorithms and phasor approaches
A newly developed hardware-friendly non-iterative fluorescence lifetime imaging (FLIM) analysis method was verified in an FPGA chip. Its performances were demonstrated on two-photon FLIM images of gold nanorods (GNRs)-Cy5 labelled Hela cells. The results obtained by the proposed method can be presented in a polor plot to be compared to the widely used phasor (Phasor) approach. Combining our met...
متن کاملPhasor-based single-molecule fluorescence lifetime imaging using a wide-field photon-counting detector.
Fluorescence lifetime imaging (FLIM) is a powerful approach to studying the immediate environment of molecules. For example, it is used in biology to study changes in the chemical environment, or to study binding processes, aggregation, and conformational changes by measuring Förster resonance energy transfer (FRET) between donor and acceptor fluorophores. FLIM can be acquired by time-domain me...
متن کاملApplying phasor approach analysis of multiphoton FLIM measurements to probe the metabolic activity of three-dimensional in vitro cell culture models
Fluorescence lifetime imaging microscopy (FLIM) can measure and discriminate endogenous fluorophores present in biological samples. This study seeks to identify FLIM as a suitable method to non-invasively detect a shift in cellular metabolic activity towards glycolysis or oxidative phosphorylation in 3D Caco-2 models of colorectal carcinoma. These models were treated with potassium cyanide or h...
متن کاملFLIM Analysis using the Phasor Plots
for the population to decrease by 1 e , or about 36.8% of the initial value. The process is accomplished with the emission photons, or fluorescence. The natural fluorescence lifetime of a fluorophore in the absence of non-radiative processes is an intrinsic property of the fluorophore. The fluorescence lifetime of a fluorescent molecule carries information about its local microenvironment and c...
متن کاملInvestigation of the Polar Representation for Td-flim
Fluorescence Lifetime Imaging Microscopy (FLIM) is a well established technique which is routinely performed in many laboratories. Since the fluorescence lifetime is sensitive to the local environment of the fluorophore (e.g. [Ca 2+ ], pH, temperature,...), FLIM was largely used to explore dynamic interactions between proteins by detecting lifetime modifications associated with Förster Resonanc...
متن کامل