He migration of macrophages, important in pathophysiological processes such as atherosclerosis and inflammatory diseases, has not been well established. This paper investigates whether the Nox2-dependent NADPH oxidase modulates the migration of macrophages and in particular to a common tissue chemoattractant, CSF-1.GSK -3203591 site Materials and Methods ReagentsAll chemicals and DMEM were purchased from Sigma. CSF-1 was purchased from RandD systems, USA. Versene for cell detachment was purchased from Gibco. Phalloidin-FITC was purchased from Sigma. Antibodies to phospho and total ERK1/2 and Akt were purchased from Cell Signalling Technology.Animal Husbandry and MaintenanceAll mice were maintained in a designated facility in accordance with the Code of Practice for the Housing and Care of Animals Used in Scientific Procedures. Mice were housed up to a maximum of 5 per cage and had free access to water and normal food chow. The mice were anaesthetised using Isoflurane (2?.5 isoflurane/oxygen). Once deep anaesthesia had been reached the mice were terminally culled by cervical dislocation. All experimental procedures were carried out under the authority of a Home Office Personal Licence and Project Licence. All animal procedures were performed following in accordance with the Guidance on the Operation of the Animals (Scientific Procedures) Act,1986 (UK Home Office) and approved by the King’s College London Animal Care and Use Committee.frame every 5 min for 18 h using AQM acquisition software (Andor, UK). Subsequently all the acquired time-lapse sequences were displayed as a movie and each cell in the first frame was tracked for the whole of the time-lapse sequence, using Motion Analysis software (Andor, UK) This resulted in the generation of a sequence of position co-ordinates relating to each cell in each frame. All the tracks were centred to co-ordinate (0,0) to better view the distance travelled. A circular horizon distance was set and the number of cells from the total population that reached the horizon distance was monitored. The random speed and the persistence in the random motion was calculated and compared. Mathematical analysis was carried out using Mathematica 6.0TM workbooks [17]. P-values less 0.05 were accepted as statistically significant. To study chemotaxis, cells were seeded on acid washed coverslips at a density of 26104 cells/ml in macrophage growth medium 15857111 and incubated overnight. Following incubation cells were starved of CSF-1 in macrophage starve medium for 8 hours. The coverslips were then mounted onto Dunn chemotaxis chambers as previously described [18] using recombinant murine CSF-1 (30 ng/ml) as the chemoattractant. Cell images were collected and analysed as described above.ImmunofluoresenceBMMs were seeded on glass coverslips at 26105 cells per coverslip and maintained in macrophage growth or macrophage starve medium followed by CSF-1 stimulation as indicated. 1317923 Cells were washed with PBS, fixed with 4 paraformaldehyde permeabilised and stained for actin using phalloidin-FITC. The actin images were collected on IX71 Olympus microscope and cell images were analysed using ImageJ.ImmunoblottingCells were seeded onto 6 well plates and maintained or CSF-1 deprived as get Gracillin outlined above. Following stimulation cells were lysed as previously described [17] and lysates subjected to acrylamide gel electrophoresis as previously described [17]. Protein membranes were blocked and probed with primary and secondary antibodies as indicated. The b.He migration of macrophages, important in pathophysiological processes such as atherosclerosis and inflammatory diseases, has not been well established. This paper investigates whether the Nox2-dependent NADPH oxidase modulates the migration of macrophages and in particular to a common tissue chemoattractant, CSF-1.Materials and Methods ReagentsAll chemicals and DMEM were purchased from Sigma. CSF-1 was purchased from RandD systems, USA. Versene for cell detachment was purchased from Gibco. Phalloidin-FITC was purchased from Sigma. Antibodies to phospho and total ERK1/2 and Akt were purchased from Cell Signalling Technology.Animal Husbandry and MaintenanceAll mice were maintained in a designated facility in accordance with the Code of Practice for the Housing and Care of Animals Used in Scientific Procedures. Mice were housed up to a maximum of 5 per cage and had free access to water and normal food chow. The mice were anaesthetised using Isoflurane (2?.5 isoflurane/oxygen). Once deep anaesthesia had been reached the mice were terminally culled by cervical dislocation. All experimental procedures were carried out under the authority of a Home Office Personal Licence and Project Licence. All animal procedures were performed following in accordance with the Guidance on the Operation of the Animals (Scientific Procedures) Act,1986 (UK Home Office) and approved by the King’s College London Animal Care and Use Committee.frame every 5 min for 18 h using AQM acquisition software (Andor, UK). Subsequently all the acquired time-lapse sequences were displayed as a movie and each cell in the first frame was tracked for the whole of the time-lapse sequence, using Motion Analysis software (Andor, UK) This resulted in the generation of a sequence of position co-ordinates relating to each cell in each frame. All the tracks were centred to co-ordinate (0,0) to better view the distance travelled. A circular horizon distance was set and the number of cells from the total population that reached the horizon distance was monitored. The random speed and the persistence in the random motion was calculated and compared. Mathematical analysis was carried out using Mathematica 6.0TM workbooks [17]. P-values less 0.05 were accepted as statistically significant. To study chemotaxis, cells were seeded on acid washed coverslips at a density of 26104 cells/ml in macrophage growth medium 15857111 and incubated overnight. Following incubation cells were starved of CSF-1 in macrophage starve medium for 8 hours. The coverslips were then mounted onto Dunn chemotaxis chambers as previously described [18] using recombinant murine CSF-1 (30 ng/ml) as the chemoattractant. Cell images were collected and analysed as described above.ImmunofluoresenceBMMs were seeded on glass coverslips at 26105 cells per coverslip and maintained in macrophage growth or macrophage starve medium followed by CSF-1 stimulation as indicated. 1317923 Cells were washed with PBS, fixed with 4 paraformaldehyde permeabilised and stained for actin using phalloidin-FITC. The actin images were collected on IX71 Olympus microscope and cell images were analysed using ImageJ.ImmunoblottingCells were seeded onto 6 well plates and maintained or CSF-1 deprived as outlined above. Following stimulation cells were lysed as previously described [17] and lysates subjected to acrylamide gel electrophoresis as previously described [17]. Protein membranes were blocked and probed with primary and secondary antibodies as indicated. The b.
