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JNK-induced MCP-1 production in spinal cord astrocytes contributes to central sensitization and neuropathic pain.

Publication ,  Journal Article
Gao, Y-J; Zhang, L; Samad, OA; Suter, MR; Yasuhiko, K; Xu, Z-Z; Park, J-Y; Lind, A-L; Ma, Q; Ji, R-R
Published in: J Neurosci
April 1, 2009

Our previous study showed that activation of c-jun-N-terminal kinase (JNK) in spinal astrocytes plays an important role in neuropathic pain sensitization. We further investigated how JNK regulates neuropathic pain. In cultured astrocytes, tumor necrosis factor alpha (TNF-alpha) transiently activated JNK via TNF receptor-1. Cytokine array indicated that the chemokine CCL2/MCP-1 (monocyte chemoattractant protein-1) was strongly induced by the TNF-alpha/JNK pathway. MCP-1 upregulation by TNF-alpha was dose dependently inhibited by the JNK inhibitors SP600125 (anthra[1,9-cd]pyrazol-6(2H)-one) and D-JNKI-1. Spinal injection of TNF-alpha produced JNK-dependent pain hypersensitivity and MCP-1 upregulation in the spinal cord. Furthermore, spinal nerve ligation (SNL) induced persistent neuropathic pain and MCP-1 upregulation in the spinal cord, and both were suppressed by D-JNKI-1. Remarkably, MCP-1 was primarily induced in spinal cord astrocytes after SNL. Spinal administration of MCP-1 neutralizing antibody attenuated neuropathic pain. Conversely, spinal application of MCP-1 induced heat hyperalgesia and phosphorylation of extracellular signal-regulated kinase in superficial spinal cord dorsal horn neurons, indicative of central sensitization (hyperactivity of dorsal horn neurons). Patch-clamp recordings in lamina II neurons of isolated spinal cord slices showed that MCP-1 not only enhanced spontaneous EPSCs but also potentiated NMDA- and AMPA-induced currents. Finally, the MCP-1 receptor CCR2 was expressed in neurons and some non-neuronal cells in the spinal cord. Together, we have revealed a previously unknown mechanism of MCP-1 induction and action. MCP-1 induction in astrocytes after JNK activation contributes to central sensitization and neuropathic pain facilitation by enhancing excitatory synaptic transmission. Inhibition of the JNK/MCP-1 pathway may provide a new therapy for neuropathic pain management.

Duke Scholars

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Published In

J Neurosci

DOI

EISSN

1529-2401

Publication Date

April 1, 2009

Volume

29

Issue

13

Start / End Page

4096 / 4108

Location

United States

Related Subject Headings

  • Up-Regulation
  • Tumor Necrosis Factor-alpha
  • Time Factors
  • Synaptic Transmission
  • Spinal Cord
  • Receptors, Tumor Necrosis Factor, Type I
  • Receptors, CCR2
  • Reaction Time
  • Patch-Clamp Techniques
  • Pain Threshold
 

Citation

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Gao, Y.-J., Zhang, L., Samad, O. A., Suter, M. R., Yasuhiko, K., Xu, Z.-Z., … Ji, R.-R. (2009). JNK-induced MCP-1 production in spinal cord astrocytes contributes to central sensitization and neuropathic pain. J Neurosci, 29(13), 4096–4108. https://doi.org/10.1523/JNEUROSCI.3623-08.2009
Gao, Yong-Jing, Ling Zhang, Omar Abdel Samad, Marc R. Suter, Kawasaki Yasuhiko, Zhen-Zhong Xu, Jong-Yeon Park, Anne-Li Lind, Qiufu Ma, and Ru-Rong Ji. “JNK-induced MCP-1 production in spinal cord astrocytes contributes to central sensitization and neuropathic pain.J Neurosci 29, no. 13 (April 1, 2009): 4096–4108. https://doi.org/10.1523/JNEUROSCI.3623-08.2009.
Gao Y-J, Zhang L, Samad OA, Suter MR, Yasuhiko K, Xu Z-Z, et al. JNK-induced MCP-1 production in spinal cord astrocytes contributes to central sensitization and neuropathic pain. J Neurosci. 2009 Apr 1;29(13):4096–108.
Gao, Yong-Jing, et al. “JNK-induced MCP-1 production in spinal cord astrocytes contributes to central sensitization and neuropathic pain.J Neurosci, vol. 29, no. 13, Apr. 2009, pp. 4096–108. Pubmed, doi:10.1523/JNEUROSCI.3623-08.2009.
Gao Y-J, Zhang L, Samad OA, Suter MR, Yasuhiko K, Xu Z-Z, Park J-Y, Lind A-L, Ma Q, Ji R-R. JNK-induced MCP-1 production in spinal cord astrocytes contributes to central sensitization and neuropathic pain. J Neurosci. 2009 Apr 1;29(13):4096–4108.

Published In

J Neurosci

DOI

EISSN

1529-2401

Publication Date

April 1, 2009

Volume

29

Issue

13

Start / End Page

4096 / 4108

Location

United States

Related Subject Headings

  • Up-Regulation
  • Tumor Necrosis Factor-alpha
  • Time Factors
  • Synaptic Transmission
  • Spinal Cord
  • Receptors, Tumor Necrosis Factor, Type I
  • Receptors, CCR2
  • Reaction Time
  • Patch-Clamp Techniques
  • Pain Threshold