Partner: Mike White

University of Manchester (GB)

Recent publications
1.Downton P., Bagnall James S., England H., Spiller David G., Humphreys Neil E., Jackson Dean A., Paszek P., White Michael R.R., Adamson Antony D., Overexpression of IκB⍺ modulates NF-κB activation of inflammatory target gene expression, Frontiers in Molecular Biosciences, ISSN: 2296-889X, DOI: 10.3389/fmolb.2023.1187187, Vol.10, pp.1187187-1-15, 2023
Abstract:

Cells respond to inflammatory stimuli such as cytokines by activation of the nuclear factor-κB (NF-κB) signalling pathway, resulting in oscillatory translocation of the transcription factor p65 between nucleus and cytoplasm in some cell types. We investigate the relationship between p65 and inhibitor-κB⍺ (IκBα) protein levels and dynamic properties of the system, and how this interaction impacts on the expression of key inflammatory genes. Using bacterial artificial chromosomes, we developed new cell models of IκB⍺-eGFP protein overexpression in a pseudo-native genomic context. We find that cells with high levels of the negative regulator IκBα remain responsive to inflammatory stimuli and maintain dynamics for both p65 and IκBα. In contrast, canonical target gene expression is dramatically reduced by overexpression of IκBα, but can be partially rescued by overexpression of p65. Treatment with leptomycin B to promote nuclear accumulation of IκB⍺ also suppresses canonical target gene expression, suggesting a mechanism in which nuclear IκB⍺ accumulation prevents productive p65 interaction with promoter binding sites. This causes reduced target promoter binding and gene transcription, which we validate by chromatin immunoprecipitation and in primary cells. Overall, we show how inflammatory gene transcription is modulated by the expression levels of both IκB⍺ and p65. This results in an anti-inflammatory effect on transcription, demonstrating a broad mechanism to modulate the strength of inflammatory response.

Keywords:

NF-κB, inflammation, IκB⍺, overexpression, gene expression, localisation

Affiliations:
Downton P.-other affiliation
Bagnall James S.-other affiliation
England H.-other affiliation
Spiller David G.-other affiliation
Humphreys Neil E.-other affiliation
Jackson Dean A.-other affiliation
Paszek P.-IPPT PAN
White Michael R.R.-University of Manchester (GB)
Adamson Antony D.-other affiliation
2.Papoutsopoulou S., Burkitt Michael D., Bergey F., England H., Hough R., Schmidt L., Spiller David G., White Michael H. R.R., Paszek P., Jackson Dean A., Martins Dos Santos Vitor A. P., Sellge G., Pritchard D. M., Campbell Barry J., Müller W., Probert Chris S., Macrophage-Specific NF-κB Activation Dynamics Can Segregate Inflammatory Bowel Disease Patients, Frontiers in Immunology, ISSN: 1664-3224, DOI: 10.3389/fimmu.2019.02168, Vol.10, pp.2168-1-11, 2019
Abstract:

The heterogeneous nature of inflammatory bowel disease (IBD) presents challenges, particularly when choosing therapy. Activation of the NF-κB transcription factor is a highly regulated, dynamic event in IBD pathogenesis. Using a lentivirus approach, NF-κB-regulated luciferase was expressed in patient macrophages, isolated from frozen peripheral blood mononuclear cell samples. Following activation, samples could be segregated into three clusters based on the NF-κB-regulated luciferase response. The ulcerative colitis (UC) samples appeared only in the hypo-responsive Cluster 1, and in Cluster 2. Conversely, Crohn's disease (CD) patients appeared in all Clusters with their percentage being higher in the hyper-responsive Cluster 3. A positive correlation was seen between NF-κB-induced luciferase activity and the concentrations of cytokines released into medium from stimulated macrophages, but not with serum or biopsy cytokine levels. Confocal imaging of lentivirally-expressed p65 activation revealed that a higher proportion of macrophages from CD patients responded to endotoxin lipid A compared to controls. In contrast, cells from UC patients exhibited a shorter duration of NF-κB p65 subunit nuclear localization compared to healthy controls, and CD donors. Analysis of macrophage cytokine responses and patient metadata revealed a strong correlation between CD patients who smoked and hyper-activation of p65. These in vitro dynamic assays of NF-κB activation in blood-derived macrophages have the potential to segregate IBD patients into groups with different phenotypes and may therefore help determine response to therapy.

Keywords:

inflammatory bowel disease, NF-kB, macrophages, cytokines, Crohn’s disease, ulcerative colitis

Affiliations:
Papoutsopoulou S.-other affiliation
Burkitt Michael D.-other affiliation
Bergey F.-other affiliation
England H.-other affiliation
Hough R.-other affiliation
Schmidt L.-other affiliation
Spiller David G.-other affiliation
White Michael H. R.R.-University of Manchester (GB)
Paszek P.-other affiliation
Jackson Dean A.-other affiliation
Martins Dos Santos Vitor A. P.-other affiliation
Sellge G.-other affiliation
Pritchard D. M.-other affiliation
Campbell Barry J.-other affiliation
Müller W.-other affiliation
Probert Chris S.-other affiliation
3.Kardyńska M., Paszek A., Śmieja J., Spiller David G., Widłak W., White Michael R. H.R., Paszek P., Kimmel M., Quantitative analysis reveals crosstalk mechanisms of heat shock-induced attenuation of NF-κB signaling at the single cell level, PLOS COMPUTATIONAL BIOLOGY, ISSN: 1553-7358, DOI: 10.1371/journal.pcbi.1006130, Vol.14, No.4, pp.e1006130-1-25, 2018
Abstract:

Elevated temperature induces the heat shock (HS) response, which modulates cell proliferation, apoptosis, the immune and inflammatory responses. However, specific mechanisms linking the HS response pathways to major cellular signaling systems are not fully understood. Here we used integrated computational and experimental approaches to quantitatively analyze the crosstalk mechanisms between the HS-response and a master regulator of inflammation, cell proliferation, and apoptosis the Nuclear Factor κB (NF-κB) system. We found that populations of human osteosarcoma cells, exposed to a clinically relevant 43°C HS had an attenuated NF-κB p65 response to Tumor Necrosis Factor α (TNFα) treatment. The degree of inhibition of the NF-κB response depended on the HS exposure time. Mathematical modeling of single cells indicated that individual crosstalk mechanisms differentially encode HS-mediated NF-κB responses while being consistent with the observed population-level responses. In particular “all-or-nothing” encoding mechanisms were involved in the HS-dependent regulation of the IKK activity and IκBα phosphorylation, while others involving transport were “analogue”. In order to discriminate between these mechanisms, we used live-cell imaging of nuclear translocations of the NF-κB p65 subunit. The single cell responses exhibited “all-or-nothing” encoding. While most cells did not respond to TNFα stimulation after a 60 min HS, 27% showed responses similar to those not receiving HS. We further demonstrated experimentally and theoretically that the predicted inhibition of IKK activity was consistent with the observed HS-dependent depletion of the IKKα and IKKβ subunits in whole cell lysates. However, a combination of “all-or-nothing” crosstalk mechanisms was required to completely recapitulate the single cell data. We postulate therefore that the heterogeneity of the single cell responses might be explained by the cell-intrinsic variability of HS-modulated IKK signaling. In summary, we show that high temperature modulates NF-κB responses in single cells in a complex and unintuitive manner, which needs to be considered in hyperthermia-based treatment strategies.

Affiliations:
Kardyńska M.-other affiliation
Paszek A.-other affiliation
Śmieja J.-Silesian University of Technology (PL)
Spiller David G.-other affiliation
Widłak W.-other affiliation
White Michael R. H.R.-University of Manchester (GB)
Paszek P.-other affiliation
Kimmel M.-Rice University (US)
4.Bagnall J., Boddington C., England H., Brignall R., Downton P., Alsoufi Z., Boyd J., Rowe W., Bennett A., Walker C., Adamson A., Patel Nisha M. X., O’Cualain R., Schmidt L., Spiller David G., Jackson Dean A., Müller W., Muldoon M., White Michael R. H.R., Paszek P., Quantitative analysis of competitive cytokine signaling predicts tissue thresholds for the propagation of macrophage activation, Science Signaling, ISSN: 1945-0877, DOI: 10.1126/scisignal.aaf3998, Vol.11, No.540, pp.1-15, 2018
Abstract:

Toll-like receptor (TLR) signaling regulates macrophage activation and effector cytokine propagation in the constrained environment of a tissue. In macrophage populations, TLR4 stimulates the dose-dependent transcription of nuclear factor κB (NF-κB) target genes. However, using single-RNA counting, we found that individual cells exhibited a wide range (three orders of magnitude) of expression of the gene encoding the proinflammatory cytokine tumor necrosis factor–α (TNF-α). The TLR4-induced TNFA transcriptional response correlated with the extent of NF-κB signaling in the cells and their size. We compared the rates of TNF-α production and uptake in macrophages and mouse embryonic fibroblasts and generated a mathematical model to explore the heterogeneity in the response of macrophages to TLR4 stimulation and the propagation of the TNF-α signal in the tissue. The model predicts that the local propagation of the TLR4-dependent TNF-α response and cellular NF-κB signaling are limited to small distances of a few cell diameters between neighboring tissue-resident macrophages. In our predictive model, TNF-α propagation was constrained by competitive uptake of TNF-α from the environment, rather than by heterogeneous production of the cytokine. We propose that the highly constrained architecture of tissues enables effective localized propagation of inflammatory cues while avoiding out-of-context responses at longer distances.

Affiliations:
Bagnall J.-other affiliation
Boddington C.-other affiliation
England H.-other affiliation
Brignall R.-other affiliation
Downton P.-other affiliation
Alsoufi Z.-other affiliation
Boyd J.-other affiliation
Rowe W.-other affiliation
Bennett A.-other affiliation
Walker C.-other affiliation
Adamson A.-other affiliation
Patel Nisha M. X.-other affiliation
O’Cualain R.-other affiliation
Schmidt L.-other affiliation
Spiller David G.-other affiliation
Jackson Dean A.-other affiliation
Müller W.-other affiliation
Muldoon M.-other affiliation
White Michael R. H.R.-University of Manchester (GB)
Paszek P.-other affiliation
5.Adamson A., Boddington C., Downton P., Rowe W., Bagnall J., Lam C., Maya-Mendoza A., Schmidt L., Harper Claire V.V., Spiller David G., Rand David A.A., Jackson Dean A., White Michael R. H.R., Paszek P., Signal transduction controls heterogeneous NF-κB dynamics and target gene expression through cytokine-specific refractory states, Nature Communications, ISSN: 2041-1723, DOI: 10.1038/ncomms12057, Vol.7, pp.12057-1-14, 2016
Abstract:

Cells respond dynamically to pulsatile cytokine stimulation. Here we report that single, or well-spaced pulses of TNFα (>100 min apart) give a high probability of NF-κB activation. However, fewer cells respond to shorter pulse intervals (<100 min) suggesting a heterogeneous refractory state. This refractory state is established in the signal transduction network downstream of TNFR and upstream of IKK, and depends on the level of the NF-κB system negative feedback protein A20. If a second pulse within the refractory phase is IL-1β instead of TNFα, all of the cells respond. This suggests a mechanism by which two cytokines can synergistically activate an inflammatory response. Gene expression analyses show strong correlation between the cellular dynamic response and NF-κB-dependent target gene activation. These data suggest that refractory states in the NF-κB system constitute an inherent design motif of the inflammatory response and we suggest that this may avoid harmful homogenous cellular activation.

Affiliations:
Adamson A.-other affiliation
Boddington C.-other affiliation
Downton P.-other affiliation
Rowe W.-other affiliation
Bagnall J.-other affiliation
Lam C.-other affiliation
Maya-Mendoza A.-other affiliation
Schmidt L.-other affiliation
Harper Claire V.V.-University of Manchester (GB)
Spiller David G.-other affiliation
Rand David A.A.-University of Warwick (GB)
Jackson Dean A.-other affiliation
White Michael R. H.R.-University of Manchester (GB)
Paszek P.-other affiliation
6.Martín-Sánchez F., Diamond C., Zeitler M., Gomez A., Baroja-Mazo A., Bagnall J., Spiller David G., White M.R., Daniels Michael J.D., Mortellaro A., Peñalver M., Paszek P., Steringer J., Nickel W., Brough D., Pelegrín P., Inflammasome-dependent IL-1β release depends upon membrane permeabilisation, Cell Death & Differentiation, ISSN: 1350-9047, DOI: 10.1038/cdd.2015.176, Vol.23, pp.1219-1231, 2016
Abstract:

Interleukin-1β (IL-1β) is a critical regulator of the inflammatory response. IL-1β is not secreted through the conventional ER–Golgi route of protein secretion, and to date its mechanism of release has been unknown. Crucially, its secretion depends upon the processing of a precursor form following the activation of the multimolecular inflammasome complex. Using a novel and reversible pharmacological inhibitor of the IL-1β release process, in combination with biochemical, biophysical, and real-time single-cell confocal microscopy with macrophage cells expressing Venus-labelled IL-1β, we have discovered that the secretion of IL-1β after inflammasome activation requires membrane permeabilisation, and occurs in parallel with the death of the secreting cell. Thus, in macrophages the release of IL-1β in response to inflammasome activation appears to be a secretory process independent of nonspecific leakage of proteins during cell death. The mechanism of membrane permeabilisation leading to IL-1β release is distinct from the unconventional secretory mechanism employed by its structural homologues fibroblast growth factor 2 (FGF2) or IL-1α, a process that involves the formation of membrane pores but does not result in cell death. These discoveries reveal key processes at the initiation of an inflammatory response and deliver new insights into the mechanisms of protein release.

Affiliations:
Martín-Sánchez F.-other affiliation
Diamond C.-other affiliation
Zeitler M.-other affiliation
Gomez A.-other affiliation
Baroja-Mazo A.-other affiliation
Bagnall J.-other affiliation
Spiller David G.-other affiliation
White M.R.-University of Manchester (GB)
Daniels Michael J.D.-other affiliation
Mortellaro A.-other affiliation
Peñalver M.-other affiliation
Paszek P.-other affiliation
Steringer J.-other affiliation
Nickel W.-other affiliation
Brough D.-other affiliation
Pelegrín P.-other affiliation
7.Ankers John M., Awais R., Jones Nicholas A., Boyd J., Ryan S., Adamson Antony D., Harper Claire V.V., Bridge L., Spiller David G., Jackson Dean A., Paszek P., Sée V., White Michael R.R., Dynamic NF-κB and E2F interactions control the priority and timing of inflammatory signalling and cell proliferation, eLife, ISSN: 2050-084X, DOI: 10.7554/eLife.10473, Vol.5, pp.e10473-1-35, 2016
Abstract:

Dynamic cellular systems reprogram gene expression to ensure appropriate cellular fate responses to specific extracellular cues. Here we demonstrate that the dynamics of Nuclear Factor kappa B (NF-κB) signalling and the cell cycle are prioritised differently depending on the timing of an inflammatory signal. Using iterative experimental and computational analyses, we show physical and functional interactions between NF-κB and the E2 Factor 1 (E2F-1) and E2 Factor 4 (E2F-4) cell cycle regulators. These interactions modulate the NF-κB response. In S-phase, the NF-κB response was delayed or repressed, while cell cycle progression was unimpeded. By contrast, activation of NF-κB at the G1/S boundary resulted in a longer cell cycle and more synchronous initial NF-κB responses between cells. These data identify new mechanisms by which the cellular response to stress is differentially controlled at different stages of the cell cycle.

Affiliations:
Ankers John M.-other affiliation
Awais R.-other affiliation
Jones Nicholas A.-Massachusetts Institute of Technology (US)
Boyd J.-other affiliation
Ryan S.-other affiliation
Adamson Antony D.-other affiliation
Harper Claire V.V.-University of Manchester (GB)
Bridge L.-other affiliation
Spiller David G.-other affiliation
Jackson Dean A.-other affiliation
Paszek P.-other affiliation
Sée V.-other affiliation
White Michael R.R.-University of Manchester (GB)
8.Finkenstädt B., Woodcock D.J., Komorowski M., Harper C.V., Davis J.R.E., White M.R.H., Rand D.A., Quantifying intrinsic and extrinsic noise in gene transcription using the linear noise approximation: An application to single cell data, Annals of Applied Statistics, ISSN: 1932-6157, DOI: 10.1214/13-AOAS669, Vol.7, No.4, pp.1960-1982, 2013
Abstract:

A central challenge in computational modeling of dynamic biological systems is parameter inference from experimental time course measurements. However, one would not only like to infer kinetic parameters but also study their variability from cell to cell. Here we focus on the case where single-cell fluorescent protein imaging time series data are available for a population of cells. Based on van Kampen’s linear noise approximation, we derive a dynamic state space model for molecular populations which is then extended to a hierarchical model. This model has potential to address the sources of variability relevant to single-cell data, namely, intrinsic noise due to the stochastic nature of the birth and death processes involved in reactions and extrinsic noise arising from the cell-to-cell variation of kinetic parameters. In order to infer such a model from experimental data, one must also quantify the measurement process where one has to allow for nonmeasurable molecular species as well as measurement noise of unknown level and variance. The availability of multiple single-cell time series data here provides a unique testbed to fit such a model and quantify these different sources of variation from experimental data.

Keywords:

Linear noise approximation, kinetic parameter estimation, intrinsic and extrinsic noise, state space model and Kalman filter, Bayesian hierarchical modeling

Affiliations:
Finkenstädt B.-University of Warwick (GB)
Woodcock D.J.-University of Warwick (GB)
Komorowski M.-IPPT PAN
Harper C.V.-University of Manchester (GB)
Davis J.R.E.-University of Manchester (GB)
White M.R.H.-University of Manchester (GB)
Rand D.A.-University of Warwick (GB)
9.Harper Claire V.V., Featherstone K., Semprini S., Friedrichsen S., McNeilly J., Paszek P., Spiller David G., McNeilly Alan S., Mullins John J., Davis Julian R., White Michael R.R., Dynamic organisation of prolactin gene expression in living pituitary tissue, Journal of Cell Science, ISSN: 0021-9533, DOI: 10.1242/jcs.060434, Vol.123, No.3, pp.424-430, 2010
Abstract:

Gene expression in living cells is highly dynamic, but temporal patterns of gene expression in intact tissues are largely unknown. The mammalian pituitary gland comprises several intermingled cell types, organised as interdigitated networks that interact functionally to generate co-ordinated hormone secretion. Live-cell imaging was used to quantify patterns of reporter gene expression in dispersed lactotrophic cells or intact pituitary tissue from bacterial artificial chromosome (BAC) transgenic rats in which a large prolactin genomic fragment directed expression of luciferase or destabilised enhanced green fluorescent protein (d2EGFP). Prolactin promoter activity in transgenic pituitaries varied with time across different regions of the gland. Although amplitude of transcriptional responses differed, all regions of the gland displayed similar overall patterns of reporter gene expression over a 50-hour period, implying overall co-ordination of cellular behaviour. By contrast, enzymatically dispersed pituitary cell cultures showed unsynchronised fluctuations of promoter activity amongst different cells, suggesting that transcriptional patterns were constrained by tissue architecture. Short-term, high resolution, single cell analyses in prolactin-d2EGFP transgenic pituitary slice preparations showed varying transcriptional patterns with little correlation between adjacent cells. Together, these data suggest that pituitary tissue comprises a series of cell ensembles, which individually display a variety of patterns of short-term stochastic behaviour, but together yield long-range and long-term coordinated behaviour.

Keywords:

Live-cell, Microscopy, Pituitary, Prolactin, Transcription

Affiliations:
Harper Claire V.V.-University of Manchester (GB)
Featherstone K.-other affiliation
Semprini S.-other affiliation
Friedrichsen S.-other affiliation
McNeilly J.-other affiliation
Paszek P.-other affiliation
Spiller David G.-other affiliation
McNeilly Alan S.-other affiliation
Mullins John J.-other affiliation
Davis Julian R.-University of Manchester (GB)
White Michael R.R.-University of Manchester (GB)
10.Ashall L., Horton Caroline A., Nelson David E., Paszek P., Harper Claire V.V., Sillitoe K., Ryan S., Spiller David G., Unitt John F., Broomhead David S., Kell Douglas B., Rand David A.A., Sée V., White Michael R.R., Pulsatile Stimulation Determines Timing and Specificity of NF-κB-Dependent Transcription, Science, ISSN: 0036-8075, DOI: 10.1126/science.1164860, Vol.324, No.5924, pp.242-246, 2009
Abstract:

The nuclear factor κB (NF-κB) transcription factor regulates cellular stress responses and the immune response to infection. NF-κB activation results in oscillations in nuclear NF-κB abundance. To define the function of these oscillations, we treated cells with repeated short pulses of tumor necrosis factor–α at various intervals to mimic pulsatile inflammatory signals. At all pulse intervals that were analyzed, we observed synchronous cycles of NF-κB nuclear translocation. Lower frequency stimulations gave repeated full-amplitude translocations, whereas higher frequency pulses gave reduced translocation, indicating a failure to reset. Deterministic and stochastic mathematical models predicted how negative feedback loops regulate both the resetting of the system and cellular heterogeneity. Altering the stimulation intervals gave different patterns of NF-κB–dependent gene expression, which supports the idea that oscillation frequency has a functional role.

Affiliations:
Ashall L.-other affiliation
Horton Caroline A.-other affiliation
Nelson David E.-other affiliation
Paszek P.-other affiliation
Harper Claire V.V.-University of Manchester (GB)
Sillitoe K.-other affiliation
Ryan S.-other affiliation
Spiller David G.-other affiliation
Unitt John F.-other affiliation
Broomhead David S.-other affiliation
Kell Douglas B.-other affiliation
Rand David A.A.-University of Warwick (GB)
Sée V.-other affiliation
White Michael R.R.-University of Manchester (GB)