Persistent TNF-alpha exposure impairs store operated calcium influx in CD4+ T lymphocytes |
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Authors: | Church Leigh D Goodall John E Rider David A Bacon Paul A Young Stephen P |
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Affiliation: | Division of Immunity and Infection, Department of Rheumatology, University of Birmingham, Edgbaston, Birmingham, B15 2TT, UK. l.d.church@bham.ac.uk |
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Abstract: | Persistent tumour necrosis factor alpha (TNF-alpha) exposure uncouples proximal T-cell receptor (TCR)-signalling events. Here, we demonstrate that chronic TNF-alpha exposure also attenuates signalling distal to the TCR, by specifically inhibiting Ca2+ influx evoked by thapsigargin in CD4+ T-cells. Mitogen-induced Ca2+ responses were impaired in a dose dependent manner, and TCR-induced Ca2+ responses were also significantly reduced. The impairment of Ca2+ influx strongly correlated with poor function as proliferative responses to both mitogen and anti-CD3/CD28 stimulation were suppressed. Our findings show that persistent TNF-alpha exposure of T-cells specifically inhibits store operated Ca2+ influx. This may affect gene activation and contribute to the poor T-cell function in chronic inflammatory disease. |
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Keywords: | Tumour necrosis factor-α Calcium (Ca2+) T-cell Store operated Ca2+ influx T-cell receptor |
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