Presence of NGF and its receptor TrkA in degenerative lumbar facet joint specimens

被引:0
|
作者
M. F. Surace
D. Prestamburgo
M. Campagnolo
A. Fagetti
L. Murena
机构
[1] Universitas Studiorum Insubriae,Department of Orthopaedic and Trauma Sciences “M. Boni”
来源
European Spine Journal | 2009年 / 18卷
关键词
Nerve growth factor; Receptor trkA; Spine; Low back pain; Osteoarthritis;
D O I
暂无
中图分类号
学科分类号
摘要
In a preliminary study, the recurrent presence of nervous terminations was demonstrated with optical microscopy in several slides of degenerative lumbar facet joints and surrounding soft tissues. The purpose of this study was to prove the presence of NGF (nerve growth factor) and its receptor TrkA (tyrosine kinase receptor) with immunofluorescence. The peri/articular tissues were harvested from the lumbar facet joints of ten patients surgically treated for degenerative diseases. There were seven females (one bilateral) and two males whose mean age at surgery was 72 years (range, 67–80 years). The affected levels were L3–L4 in two cases and L4–L5 in seven cases (one bilateral). All specimens were fixed in formalin, dehydrated and enclosed in paraffin. From each specimen, four slides were obtained. Two slides were employed for the search of NGF: one was treated with specific antibodies and marked with FITC (fluorescein isothiocyanate conjugated), and the second slide was for control purposes. It was exposed to FITC, but without prior exposure to the specific antibody. The same procedure was repeated to obtain on two more slides, to repeat the search for Trka with specific antibodies. All the slides were finally studied on a fluoromicroscope. The analysis of these specimens revealed the presence of the neurotrophin (NGF) and its own receptor (TrkA) in all cases: the immunohistochemical reaction between the specimens and the specific antibodies marked with FITC was seen under fluoromicroscopy, but in none of the control cases treated with FITC only. NGF is released by mastocytes, fibroblasts and other cell types involved in the inflammatory processes. The level of peripheral NGF is increased in inflammatory processes, while the administration of exogenous NGF has a hyperalgesic effect on rats and produces muscular pain in humans. Furthermore, NGF produces hypersensitization to heat stimulation in humans and mammals in general. There is considerable evidence showing that the system constituted by the NGF and its high-affinity receptor TrkA plays a fundamental role in the molecular processes underlying the main forms of “persistent” pain. This indicates a possible therapeutic area for the antibodies that could block the NGF/TrkA system, in order to modulate the frequency and the duration of the action potential of nociceptive neurons during chronic inflammation. This study demonstrated the presence of NGF and TrkA in specimens collected from degenerative facet joints, suggesting that specific molecules could be used in order to modulate chronic pain in patients with degenerative lumbar spine.
引用
收藏
页码:122 / 125
页数:3
相关论文
共 50 条
  • [41] The Neurotrophic Tyrosine Kinase Receptor TrkA and Its Ligand NGF are Increased in Squamous Cell Carcinomas of the Lung
    Gao, Fangfang
    Griffin, Nathan
    Faulkner, Sam
    Rowe, Christopher W.
    Williams, Lily
    Roselli, Severine
    Thorne, Rick F.
    ASIA-PACIFIC JOURNAL OF CLINICAL ONCOLOGY, 2018, 14 : 20 - 20
  • [42] The neurotrophic tyrosine kinase receptor TrkA and its ligand NGF are increased in squamous cell carcinomas of the lung
    Gao, Fangfang
    Griffin, Nathan
    Faulkner, Sam
    Rowe, Christopher W.
    Williams, Lily
    Roselli, Severine
    Thorne, Rick F.
    Ferdoushi, Aysha
    Jobling, Phillip
    Walker, Marjorie M.
    Hondermarck, Hubert
    SCIENTIFIC REPORTS, 2018, 8
  • [43] The neurotrophic tyrosine kinase receptor TrkA and its ligand NGF are increased in squamous cell carcinomas of the lung
    Fangfang Gao
    Nathan Griffin
    Sam Faulkner
    Christopher W. Rowe
    Lily Williams
    Severine Roselli
    Rick F. Thorne
    Aysha Ferdoushi
    Phillip Jobling
    Marjorie M. Walker
    Hubert Hondermarck
    Scientific Reports, 8
  • [44] Characterization of the recombinant extracellular domain of the neurotrophin receptor TrkA and its interaction with nerve growth factor (NGF)
    Woo, SB
    Whalen, C
    Neet, KE
    PROTEIN SCIENCE, 1998, 7 (04) : 1006 - 1016
  • [45] MMP-1 overexpression induced by IL-1β: possible mechanism for inflammation in degenerative lumbar facet joint
    Xu, Dawei
    Sun, Yuyu
    Bao, Guofeng
    Liu, Wei
    Zhu, Xinhui
    Cui, Shengyu
    Fan, Jianbo
    Cui, Zhiming
    JOURNAL OF ORTHOPAEDIC SCIENCE, 2013, 18 (06) : 1012 - 1019
  • [46] Human lumbar spine facet joint osteoarthritis displays predominant NGF expression and signaling in synovial and subchondral bone marrow tissues
    Seidel, M. F.
    Busso, N.
    Chobaz, V
    Netzer, C.
    Huegle, T.
    Geurts, J.
    SWISS MEDICAL WEEKLY, 2019, : 4S - 4S
  • [47] The relationship between the prevalance and size of lumbar ossified ligamentum flavum and the presence and degree of facet joint degeneration
    Ergun, Tarkan
    Lakadamyali, Hatice
    EUROPEAN JOURNAL OF RADIOLOGY, 2012, 81 (11) : 3456 - 3460
  • [48] Atherosclerotic Disease and its Relationship to Lumbar Degenerative Disk Disease, Facet Arthritis, and Stenosis With Computed Tomography Angiography
    Beckworth, William J.
    Holbrook, John F.
    Foster, Lisa G.
    Ward, Laura A.
    Welle, James R.
    PM&R, 2018, 10 (04) : 331 - 337
  • [49] Prevalence of lumbar facet arthrosis and its relationship to age, sex, and race - An anatomic study of cadaveric specimens
    Eubanks, Jason David
    Lee, Michael J.
    Cassinelli, Ezequiel
    Ahn, Nicholas U.
    SPINE, 2007, 32 (19) : 2058 - 2062
  • [50] Can facet joint fluid on MRI and dynamic instability be a predictor of improvement in back pain following lumbar fusion for degenerative spondylolisthesis?
    Mark C. Snoddy
    John A. Sielatycki
    Ahilan Sivaganesan
    Stephen M. Engstrom
    Matthew J. McGirt
    Clinton J. Devin
    European Spine Journal, 2016, 25 : 2408 - 2415