Human olfactory neuroepithelial cells: tyrosine phosphorylation and process extension are increased by the combination of IL-1beta, IL-6, NGF, and bFGF

Exp Neurol. 1996 Nov;142(1):179-94. doi: 10.1006/exnr.1996.0189.

Abstract

Olfactory neuroepithelial cells (ONC) grown from biopsies of human donors are a novel cell culture system that may facilitate studies into normal and disease-related human neurobiology. We further characterized the expression of cell surface markers and intermediate filaments, and responses to neurotrophic factors by ONC. ONC are positive for cell surface markers N-CAM, PSA-N-CAM, neutral endopeptidase, N-aminopeptidase, NGF low-affinity receptor homologue (CD40), and transferrin receptor by flow cytometry for the intermediate filament proteins peripherin, vimentin, and NF-H by immunocytochemistry. Responses to neurotrophic factors measured were process outgrowth, cytoskeletal protein expression, and protein phosphorylation. Process outgrowth was increased by interleukin-beta 164-171 (IL-1beta) or by the combination of IL-1beta, interleukin-6 (IL-6), nerve growth factor (NGF), and basic fibroblast growth factor (bFGF). This combination of IL-1beta, IL-6, NGF, and bFGF (16NF) increased expression of two cytoskeletal proteins, NF-H protein and microtubule-associated protein tau. Application of the individual neurotrophic factors IL-1beta, IL-6, NGF, and bFGF increased protein phosphorylation, while 16NF produced an immediate increase in tyrosine phosphorylation of several proteins (MW of 40-80, 120, 150, and 190 kDa). The 16NF combination appears to act through a tyrosine-kinase-mediated pathway to induce process extension and increase NF-H expression. The ONC culture has the potential to be further explored to examine the relationship among process outgrowth, protein phosphorylation, and synergy between neurotrophin and cytokine receptor systems.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Antigens, CD / analysis
  • Antigens, Differentiation, B-Lymphocyte / analysis
  • Biomarkers
  • CD13 Antigens / analysis
  • CD40 Antigens / analysis
  • Cell Differentiation / drug effects
  • Cytoskeletal Proteins / drug effects
  • Cytoskeletal Proteins / metabolism
  • Epithelium / chemistry
  • Epithelium / drug effects
  • Epithelium / enzymology
  • Eye Proteins / analysis
  • Fibroblast Growth Factor 2 / pharmacology*
  • Flow Cytometry
  • GAP-43 Protein
  • GTP-Binding Proteins / analysis
  • Humans
  • Immunohistochemistry
  • Interleukin-1 / pharmacology*
  • Interleukin-6 / pharmacology*
  • Intermediate Filament Proteins / analysis
  • Membrane Glycoproteins / analysis
  • Microtubule-Associated Proteins / analysis
  • Neprilysin / analysis
  • Nerve Growth Factors / pharmacology*
  • Nerve Tissue Proteins / analysis
  • Neural Cell Adhesion Molecules / analysis
  • Neurofilament Proteins / analysis
  • Neuropeptides / analysis
  • Olfactory Mucosa
  • Olfactory Nerve
  • Olfactory Pathways / cytology*
  • Olfactory Pathways / enzymology
  • Olfactory Receptor Neurons
  • Peripherins
  • Phosphorylation
  • Protein-Tyrosine Kinases / metabolism
  • Receptors, Transferrin
  • Signal Transduction / physiology
  • Tyrosine / drug effects
  • Tyrosine / metabolism*
  • Vimentin / analysis

Substances

  • Antigens, CD
  • Antigens, Differentiation, B-Lymphocyte
  • Biomarkers
  • CD40 Antigens
  • CD71 antigen
  • Cytoskeletal Proteins
  • Eye Proteins
  • GAP-43 Protein
  • Interleukin-1
  • Interleukin-6
  • Intermediate Filament Proteins
  • Membrane Glycoproteins
  • Microtubule-Associated Proteins
  • Nerve Growth Factors
  • Nerve Tissue Proteins
  • Neural Cell Adhesion Molecules
  • Neurofilament Proteins
  • Neuropeptides
  • PRPH protein, human
  • Peripherins
  • Receptors, Transferrin
  • Vimentin
  • neurofilament protein L
  • Fibroblast Growth Factor 2
  • neurofilament protein H
  • Tyrosine
  • Protein-Tyrosine Kinases
  • CD13 Antigens
  • Neprilysin
  • GTP-Binding Proteins