The Constitutive Activation of Extracellular Signal-Regulated Kinase 1 and 2 in Periodontal Ligament Nerve Fibers

被引:6
作者
Korkmaz, Yueksel [1 ]
Bloch, Wilhelm [2 ]
Klinz, Franz-Josef [3 ]
Kuebler, Alexander C. [4 ]
Schneider, Kurt [1 ]
Zimmer, Stefan [5 ]
Addicks, Klaus [3 ]
Raab, Wolfgang H. -M. [1 ]
机构
[1] Univ Dusseldorf, Dept Operat & Prevent Dent & Endodont, D-40225 Dusseldorf, Germany
[2] German Sports Univ, Dept Mol & Cellular Sports Med, Cologne, Germany
[3] Univ Cologne, Dept Anat 1, Cologne, Germany
[4] Univ Wurzburg, Dept Oral & Maxillofacial Surg, Wurzburg, Germany
[5] Univ Witten Herdecke, Dept Operat & Prevent Dent, Witten, Germany
关键词
Extracellular signal-regulated kinases; mitogen-activated protein kinase; nociception; periodontal ligament; PRIMARY AFFERENT NEURONS; NOCICEPTIVE NEURONS; SYNAPTIC PLASTICITY; SENSORY NEURONS; PROTEIN-KINASE; MAP KINASE; PAIN; PHOSPHORYLATION; SENSITIZATION; MECHANISMS;
D O I
10.1902/jop.2009.080550
中图分类号
R78 [口腔科学];
学科分类号
1003 ;
摘要
Background: The extracellular signal-regulated kinases 1 and 2 (ERK 1/2) have been implicated in the inflammation-dependent sensitization of nociceptors. Because the periodontal ligament (PDL) contains numerous nociceptors and mechanoceptors, phosphorylation of ERK1/2 was investigated in nerve fibers of the PDL to elucidate the role of constitutive local activation of ERK1/2 in peripheral sensitization. Methods: Decalcified free-floating sections of rat molars with PDL were incubated using total (t)-ERK1/2 and phosphorylated (p)-ERK1/2 antibodies. For identification of nerve fibers in the PDL, double staining was performed using protein gene product 9.5 (PGP 9.5) with p-ERK 1/2. To test whether p-ERK1/2 activated in sensory and mechanoreceptive terminals, double incubations were performed using p-ERK1/2 with calcitonin gene-related peptide (CGRP) and with calretinin. Labeled nerve fibers were quantified by the point-counting method. Results: In cervical, midroot, and apical zones of the PDL, t-ERK1/2- and p-ERK1/2-labeled nerve fibers were found in close association with blood vessels. The p-ERK1/2-labeled free nerve fibers were often detected in cervical and apical areas of the PDL. In nerve fibers of the PDL, p-ERK1/2 was colocalized with PGP 9.5, CGRP, and calretinin. Conclusions: The perivascular distribution of t-ERK1/2 and p-ERK 1/2 in nerve fibers in the PDL is compatible with a role for the constitutive activation of ERK1/2 in the neural regulation of blood vessels in the PDL. The colocalizations of p-ERK 1/2 with CGRP and calretinin indicate that ERK1/2 is constitutively activated in a subpopulation of sensory and mechanoreceptive nerve terminals in the PDL. J Periodontol 2009;80:850-859.
引用
收藏
页码:850 / 859
页数:10
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