Up-Regulation of P2X 4 Receptors in Spinal Microglia after Peripheral Nerve Injury Mediates BDNF Release and Neuropathic Pain
ATP is a known mediator of inflammatory and neuropathic pain. However, the mechanisms by which specific purinergic receptors contribute to chronic pain states are still poorly characterized. Here, we demonstrate that in response to peripheral nerve injury, P2X 4 receptors (P2X 4 R) are expressed de...
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Published in | The Journal of neuroscience Vol. 28; no. 44; pp. 11263 - 11268 |
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Main Authors | , , , , , , , , , |
Format | Journal Article |
Language | English |
Published |
29.10.2008
|
Online Access | Get full text |
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Summary: | ATP is a known mediator of inflammatory and neuropathic pain. However, the mechanisms by which specific purinergic receptors contribute to chronic pain states are still poorly characterized. Here, we demonstrate that in response to peripheral nerve injury, P2X
4
receptors (P2X
4
R) are expressed
de novo
by activated microglia in the spinal cord. Using
in vitro
and
in vivo
models, we provide direct evidence that P2X
4
R stimulation leads to the release of BDNF from activated microglia and, most likely phosphorylation of the NR1 subunit of NMDA receptors in dorsal horn neurons of the spinal cord. Consistent with these findings, P2X4-deficient mice lack mechanical hyperalgesia induced by peripheral nerve injury and display impaired BDNF signaling in the spinal cord. Furthermore, ATP stimulation is unable to stimulate BDNF release from P2X
4
-deficient mice microglia in primary cultures. These results indicate that P2X
4
R contribute to chronic pain through a central inflammatory pathway. P2X
4
R might thus represent a potential therapeutic target to limit microglia-mediated inflammatory responses associated with brain injury and neurodegenerative disorders. |
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ISSN: | 0270-6474 1529-2401 |
DOI: | 10.1523/JNEUROSCI.2308-08.2008 |