Neurotrophins in cultured cells from periodontal tissues

J Periodontol. 2003 Jan;74(1):76-84. doi: 10.1902/jop.2003.74.1.76.

Abstract

We review the basic functions of neurotrophins and their receptors and discuss the expression and functions of neurotrophins and their specific receptors based on recent data using cultured cells from human periodontal tissues. Neurotrophins, nerve growth factor (NGF), brain-derived neurotrophic factor (BDNF), and neurotrophin-3 (NT-3) play crucial roles in the differentiation and survival of neural cells. Neurotrophins activate 2 different receptor classes: the tropomyosin-related kinase (Trk) family of receptor tyrosine kinases (TrkA, TrkB, and TrkC) and the p75 receptor, a member of the tumor necrosis factor receptor superfamily. Neurotrophins regulate both cell death and cell survival through activations of Trk receptors and/or p75 neurotrophin receptor. It has been reported that neurotrophins are also produced from non-neuronal cells, such as leukocytes, osteoblasts, or fibroblasts, and act in many other ways on non-neuronal cells. Neurotrophin expression during bone fracture healing is especially interesting, and neurotrophins are now implicated in hard tissue regeneration. It is well known that neurotrophins and their receptors are expressed in tooth development. Recent studies have found that neurotrophins and Trk receptors are expressed in mouse osteoblastic cell lines. Human periodontal ligament cells, human gingival fibroblasts, and human gingival keratinocytes expressed mRNA for NGF and TrkA. The secretion of bioactive NGF peptides from human periodontal ligament cells and human gingival keratinocytes was confirmed by bioassay using PC12 cells (rat adrenal pheochromocytoma cells). The expression of NGF and TrkA.mRNA was regulated by interleukin (IL)-1beta. NGF increased DNA synthesis and expressions of mRNA for bone-related proteins, alkaline phosphatase, and osteopontin in human periodontal ligament cells. Neurotrophins and Trk receptors expressed in human periodontal tissue may contribute to regeneration as well as innervation of periodontal tissue through local autocrine and paracrine pathways. Recent data suggest that some functions of neurotrophins and Trk receptors relate to periodontal disease and periodontal tissue regeneration. However, in vivo studies will be required to clarify the roles of neurotrophins and their receptors, including p75, in periodontal disease and periodontal tissue regeneration.

Publication types

  • Research Support, Non-U.S. Gov't
  • Review

MeSH terms

  • Alkaline Phosphatase / metabolism
  • Animals
  • Autocrine Communication / physiology
  • Brain-Derived Neurotrophic Factor / physiology
  • Cell Death / physiology
  • Cell Differentiation / physiology
  • Cell Survival / physiology
  • Cells, Cultured
  • Fibroblasts / physiology
  • Gingiva / cytology
  • Humans
  • Interleukin-1 / physiology
  • Keratinocytes / physiology
  • Mice
  • Nerve Growth Factors / physiology*
  • Neurons / physiology
  • Neurotrophin 3 / physiology
  • Osteopontin
  • Paracrine Communication / physiology
  • Periodontal Ligament / cytology
  • Periodontium / cytology
  • Periodontium / physiology*
  • Phosphoproteins / metabolism
  • Protein Kinases / physiology
  • Rats
  • Receptor Protein-Tyrosine Kinases / physiology
  • Receptors, Nerve Growth Factor / physiology
  • Receptors, Tumor Necrosis Factor / physiology
  • Regeneration / physiology
  • Sialoglycoproteins / metabolism
  • Tropomyosin / physiology

Substances

  • Brain-Derived Neurotrophic Factor
  • Interleukin-1
  • Nerve Growth Factors
  • Neurotrophin 3
  • Phosphoproteins
  • Receptors, Nerve Growth Factor
  • Receptors, Tumor Necrosis Factor
  • SPP1 protein, human
  • Sialoglycoproteins
  • Spp1 protein, mouse
  • Spp1 protein, rat
  • Tropomyosin
  • Osteopontin
  • Protein Kinases
  • Receptor Protein-Tyrosine Kinases
  • tropomyosin kinase
  • Alkaline Phosphatase