Cell signaling via the P2X nucleotide receptor: Linkage to ROS production, gene transcription, and receptor trafficking
Purinergic Signalling, ISSN: 1573-9538, Vol: 5, Issue: 2, Page: 175-187
2009
- 48Citations
- 69Captures
Metric Options: CountsSelecting the 1-year or 3-year option will change the metrics count to percentiles, illustrating how an article or review compares to other articles or reviews within the selected time period in the same journal. Selecting the 1-year option compares the metrics against other articles/reviews that were also published in the same calendar year. Selecting the 3-year option compares the metrics against other articles/reviews that were also published in the same calendar year plus the two years prior.
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Example: if you select the 1-year option for an article published in 2019 and a metric category shows 90%, that means that the article or review is performing better than 90% of the other articles/reviews published in that journal in 2019. If you select the 3-year option for the same article published in 2019 and the metric category shows 90%, that means that the article or review is performing better than 90% of the other articles/reviews published in that journal in 2019, 2018 and 2017.
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Metrics Details
- Citations48
- Citation Indexes48
- 48
- CrossRef42
- Captures69
- Readers69
- 69
Article Description
Extracellular nucleotides can act as important intercellular signals in diverse biological processes, including the enhanced production of factors that are key to immune response regulation. One receptor that binds extracellular adenosine triphosphate released at sites of infection and injury is P2X, which is an ionotrophic receptor that can also lead to the formation of a non-specific pore, activate multiple mitogen-activated protein kinases (MAPKs), and stimulate the production of immune mediators including interleukin family members and reactive oxygen species (ROS). In the present report, we have investigated the signaling mechanisms by which P2X promotes monocytic cell mediator production and induces transcription factor expression/phosphorylation, as well as how receptor-associated pore activity is regulated by intracellular trafficking. We report that P2X stimulates ROS production in macrophages through the MAPKs ERK1/2 and the nicotinamide adenine dinucleotide phosphate oxidase complex, activates several transcription factors including cyclic-AMP response element-binding protein and components of the activating protein-1 complex, and contains specific sequences within its intracellular C-terminus that appear critical for its activity. Altogether, these data further implicate P2X activation and signaling as a fundamental modulator of macrophage immune responses. © Springer Science+Business Media B.V. 2009.
Bibliographic Details
http://www.scopus.com/inward/record.url?partnerID=HzOxMe3b&scp=67349098560&origin=inward; http://dx.doi.org/10.1007/s11302-009-9133-7; http://www.ncbi.nlm.nih.gov/pubmed/19263245; http://link.springer.com/10.1007/s11302-009-9133-7; http://www.springerlink.com/index/10.1007/s11302-009-9133-7; http://www.springerlink.com/index/pdf/10.1007/s11302-009-9133-7; https://dx.doi.org/10.1007/s11302-009-9133-7; https://link.springer.com/article/10.1007/s11302-009-9133-7
Springer Science and Business Media LLC
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