Tion of NADPH oxidase [37]. Moreover, actin activates Nox2 in neutrophils in

Tion of NADPH oxidase [37]. Moreover, actin activates Nox2 in neutrophils in a cell-free system, implying their direct effect on NADPH oxidase enzyme activity, and the destabilization of the actin cytoskeleton robustly enhances the neutrophil respiratory burst activity [38,39]. A more complete understanding of this bidirectional relation between NADPH oxidases and the actin cytoskeleton may shed further light on how it mediates migration. The significantly reduced phosphorylation of ERK1/2 was in line with its important role in cellular migration and that of Nox2 in the activation of Ras/Raf/MEK/ERK signalling cascade downstream from the tyrosine receptors. ERK1/2 localise to the cell membrane [40] and to focal adhesions [41] and promote lamellipodium formation and spreading in epithelial cells [42]. Smith et al found that ERK1/2 activity was reduced in PAK12/2 BMMs which displayed spreading defects compared with WT BMMs thus suggesting that optimal activation of ERK1/2 is required during BMM spreading. [19] We also found reduced activation of ERK1/2 in the Nox2KO BMM following CSF-1 stimulation suggesting a possible mechanism whereby Nox2 generated ROS is able to modulate the downstream response via activation of ERK. Our data points to an involvement of NOX2 in BMM migration. It is interesting to note that different isoforms ofFigure 4. Nox2KO BMMs cannot chemotax towards a source of CSF-1. A) WT and Nox2KO BMMs were seeded on glass coverslips, deprived of CSF-1 and then placed in a gradient of CSF-1 using the Dunn chemotaxis Filgotinib chemical information chamber. Cells were tracked and the tracks re-set to co-ordinate (0,0) and represented by a circular histogram where the mean direction of cells is represented by a red arrow with 95 confidence interval (green wedge). Representative of three independent experiments. B and C) mean cell speed and mean persistence of direction were calculated from the tracks generated in (A). ** = p,0.001. doi:10.1371/journal.pone.0054869.gNox2 and ChemotaxisFigure 5. Nox2KO BMMs have reduced ERK phosphorylation downstream of CSF-1. A) WT and Nox2KO BMMs were CSF-1 deprived, then re-stimulated with CSF-1for the times indicated. Cells were lysed and probed for pAKt, pERK and total protein.B) Entospletinib site autoradiographs were analysed using AndorIQ and levels of pERK1, pERK2 and pAKT were normalised to loading controls. Data represents three independent experiments. * 15857111 = p,0.05. doi:10.1371/journal.pone.0054869.gNADPH oxidase have also been shown to be involved in the migration of other cell types. Nox4 has also recently been found to be a key player in the regulation of stress fibre formation and focal adhesion turnover in VSMCs [11]. These findings suggest a potentially novel mechanism of local ROS production by which focal adhesion turnover 24786787 is coordinated. Certainly a role of Nox2 in the regulation of such adhesion formation in BMM could explain the difference observed in their shape and then in their speed and persistence. Further studies of differences in the expression of integrins would increase the understanding of the exact underlying mechanism whereby the loss of Nox2 results in a reduction in the speed of migration in BMM. An important role for Nox1 in the migration of VSMC to bFGF agonist stimulation has also been identified [43] in rat SMC where inhibition of Nox1 significantly blocked migration. In summary in order to initiate inflammation and tissue repair, the migration of macrophages into tissue is an important initial step. Howev.Tion of NADPH oxidase [37]. Moreover, actin activates Nox2 in neutrophils in a cell-free system, implying their direct effect on NADPH oxidase enzyme activity, and the destabilization of the actin cytoskeleton robustly enhances the neutrophil respiratory burst activity [38,39]. A more complete understanding of this bidirectional relation between NADPH oxidases and the actin cytoskeleton may shed further light on how it mediates migration. The significantly reduced phosphorylation of ERK1/2 was in line with its important role in cellular migration and that of Nox2 in the activation of Ras/Raf/MEK/ERK signalling cascade downstream from the tyrosine receptors. ERK1/2 localise to the cell membrane [40] and to focal adhesions [41] and promote lamellipodium formation and spreading in epithelial cells [42]. Smith et al found that ERK1/2 activity was reduced in PAK12/2 BMMs which displayed spreading defects compared with WT BMMs thus suggesting that optimal activation of ERK1/2 is required during BMM spreading. [19] We also found reduced activation of ERK1/2 in the Nox2KO BMM following CSF-1 stimulation suggesting a possible mechanism whereby Nox2 generated ROS is able to modulate the downstream response via activation of ERK. Our data points to an involvement of NOX2 in BMM migration. It is interesting to note that different isoforms ofFigure 4. Nox2KO BMMs cannot chemotax towards a source of CSF-1. A) WT and Nox2KO BMMs were seeded on glass coverslips, deprived of CSF-1 and then placed in a gradient of CSF-1 using the Dunn chemotaxis chamber. Cells were tracked and the tracks re-set to co-ordinate (0,0) and represented by a circular histogram where the mean direction of cells is represented by a red arrow with 95 confidence interval (green wedge). Representative of three independent experiments. B and C) mean cell speed and mean persistence of direction were calculated from the tracks generated in (A). ** = p,0.001. doi:10.1371/journal.pone.0054869.gNox2 and ChemotaxisFigure 5. Nox2KO BMMs have reduced ERK phosphorylation downstream of CSF-1. A) WT and Nox2KO BMMs were CSF-1 deprived, then re-stimulated with CSF-1for the times indicated. Cells were lysed and probed for pAKt, pERK and total protein.B) autoradiographs were analysed using AndorIQ and levels of pERK1, pERK2 and pAKT were normalised to loading controls. Data represents three independent experiments. * 15857111 = p,0.05. doi:10.1371/journal.pone.0054869.gNADPH oxidase have also been shown to be involved in the migration of other cell types. Nox4 has also recently been found to be a key player in the regulation of stress fibre formation and focal adhesion turnover in VSMCs [11]. These findings suggest a potentially novel mechanism of local ROS production by which focal adhesion turnover 24786787 is coordinated. Certainly a role of Nox2 in the regulation of such adhesion formation in BMM could explain the difference observed in their shape and then in their speed and persistence. Further studies of differences in the expression of integrins would increase the understanding of the exact underlying mechanism whereby the loss of Nox2 results in a reduction in the speed of migration in BMM. An important role for Nox1 in the migration of VSMC to bFGF agonist stimulation has also been identified [43] in rat SMC where inhibition of Nox1 significantly blocked migration. In summary in order to initiate inflammation and tissue repair, the migration of macrophages into tissue is an important initial step. Howev.