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Adrenoceptor Expression during Intervertebral Disc Degeneration

  • Johannes Kupka
  • , Annika Kohler
  • , Karima El Bagdadi
  • , Richard Bostelmann
  • , Marco Brenneis
  • , Christoph Fleege
  • , Danny Chan
  • , Frank Zaucke
  • , Andrea Meurer
  • , Marcus Rickert
  • , Zsuzsa Jenei-Lanzl
  • Dr. Rolf M. Schwiete Research Unit for Osteoarthritis
  • Orthopedic University Hospital Friedrichsheim gGmbH
  • The Chinese University of Hong Kong

Research output: Contribution to journalOriginal Articlepeer-review

Abstract

Healthy and degenerating intervertebral discs (IVDs) are innervated by sympathetic nerves, however, adrenoceptor (AR) expression and functionality have never been investigated systematically. Therefore, AR gene expression was analyzed in both tissue and isolated cells from degenerated human IVDs. Furthermore, human IVD samples and spine sections of wildtype mice (WT) and of a mouse line that develops spontaneous IVD degeneration (IVDD, in SM/J mice) were stained for ARs and extracellular matrix (ECM) components. In IVD homogenates and cells α1a-, α1b-, α2a-, α2b-, α2c-, β1-, and β2-AR genes were expressed. In human sections, β2-AR was detectable, and its localization parallels with ECM alterations. Similarly, in IVDs of WT mice, only β2-AR was expressed, and in IVDs of SM/J mice, β2AR expression was stronger accompanied by increased collagen II, collagen XII, decorin as well as decreased cartilage oligomeric matrix protein expression. In addition, norepinephrine stimulation of isolated human IVD cells induced intracellular signaling via ERK1/2 and PKA. For the first time, the existence and functionality of ARs were demonstrated in IVD tissue samples, suggesting that the sympathicus might play a role in IVDD. Further studies will address relevant cellular mechanisms and thereby help to develop novel therapeutic options for IVDD.

Original languageEnglish
JournalINTERNATIONAL JOURNAL OF MOLECULAR SCIENCES
Volume21
Issue number6
DOIs
Publication statusPublished - 18 Mar 2020
Externally publishedYes

Keywords

  • Aged
  • Animals
  • Female
  • Gene Expression Regulation
  • Humans
  • Intervertebral Disc Degeneration/metabolism
  • MAP Kinase Signaling System
  • Male
  • Mice
  • Mice, Transgenic
  • Mitogen-Activated Protein Kinase 1/metabolism
  • Mitogen-Activated Protein Kinase 3/metabolism
  • Receptors, Adrenergic/biosynthesis

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