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Andres, C.* ; Hasenauer, J. ; Ahn, H.S.* ; Joseph, E.K.* ; Isensee, J.* ; Theis, F.J. ; Allgöwer, F.* ; Levine, J.D.* ; Dib-Hajj, S.D.* ; Waxman, S.G.* ; Hucho, T.*

Wound-healing growth factor, basic FGF, induces Erk1/2-dependent mechanical hyperalgesia.

Pain 154, 2216-2226 (2013)
DOI PMC
Open Access Gold möglich sobald Verlagsversion bei der ZB eingereicht worden ist.
Growth factors such as nerve growth factor and glial cell line-derived neurotrophic factor are known to induce pain sensitization. However, a plethora of other growth factors is released during inflammation and tissue regeneration, and many of them are essential for wound healing. Which wound-healing factors also alter the sensitivity of nociceptive neurons is not well known. We studied the wound-healing factor, basic fibroblast growth factor (bFGF), for its role in pain sensitization. Reverse transcription polymerase chain reaction showed that the receptor of bFGF, FGFR1, is expressed in lumbar rat dorsal root ganglia (DRG). We demonstrated presence of FGFR1 protein in DRG neurons by a recently introduced quantitative automated immunofluorescent microscopic technique. FGFR1 was expressed in all lumbar DRG neurons as quantified by mixture modeling. Corroborating the mRNA and protein expression data, bFGF induced Erk1/2 phosphorylation in nociceptive neurons, which could be blocked by inhibition of FGF receptors. Furthermore, bFGF activated Erk1/2 in a dose- and time-dependent manner. Using single-cell electrophysiological recordings, we found that bFGF treatment of DRG neurons increased the current-density of NaV1.8 channels. Erk1/2 inhibitors abrogated this increase. Importantly, intradermal injection of bFGF in rats induced Erk1/2-dependent mechanical hyperalgesia. Perspective: Analyzing intracellular signaling dynamics in nociceptive neurons has proven to be a powerful approach to identify novel modulators of pain. In addition to describing a new sensitizing factor, our findings indicate the potential to investigate wound-healing factors for their role in nociception.
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Publikationstyp Artikel: Journalartikel
Dokumenttyp Wissenschaftlicher Artikel
Schlagwörter Pain ; Nociception ; Peripheral Sensory Neuron ; Sensitization Signaling ; Inflammatory Pain ; Wound Healing ; Quantitative Automated Microscopy ; Bfgf ; Fgf-2 ; Fgf-beta ; Map Kinase ; Erk1/2 ; Na(v)1.8 ; Voltage Gated Sodium Channels ; Randall Selitto; Nociceptive Sensory Neurons ; Protein-kinase-c ; Congenital Insensitivity ; Neurogenic Inflammation ; Rheumatoid-arthritis ; Tyrosine Kinase ; Sodium-channels ; Messenger-rna ; Nerve Injury ; Pain
Sprache englisch
Veröffentlichungsjahr 2013
HGF-Berichtsjahr 2013
ISSN (print) / ISBN 0304-3959
e-ISSN 1872-6623
Zeitschrift Pain
Quellenangaben Band: 154, Heft: 10, Seiten: 2216-2226 Artikelnummer: , Supplement: ,
Verlag Elsevier
Begutachtungsstatus Peer reviewed
Institut(e) Institute of Bioinformatics and Systems Biology (IBIS)
POF Topic(s) 30505 - New Technologies for Biomedical Discoveries
Forschungsfeld(er) Enabling and Novel Technologies
PSP-Element(e) G-503700-004
PubMed ID 23867734
DOI 10.1016/j.pain.2013.07.005
WOS ID WOS:000324475500040
Scopus ID 84884291453
Erfassungsdatum 2013-09-23
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