J1/tenascin in substrate-bound and soluble form displays contrary effects on neurite outgrowth

J Cell Biol. 1991 Jun;113(5):1159-71. doi: 10.1083/jcb.113.5.1159.

Abstract

The influence of J1/tenascin adsorbed to polyornithine-conditioned plastic (substrate-bound J1/tenascin) and J1/tenascin present in the culture medium (soluble J1/tenascin) on neurite outgrowth was studied with cultured single cells from hippocampus and mesencephalon of embryonic rats. Neurons at low density grew well on J1/tenascin substrates and extended neurites that were approximately 40% longer than on the polyornithine control substrate after 24 h in vitro. The neurite outgrowth promoting effect of substrate bound J1/tenascin was largely abolished in the presence of mAb J1/tn2, but not by mAb J1/tn1. In contrast to the neurite growth-promoting effects of substrate bound J1/tenascin, neurite outgrowth on polyornithine, laminin, fibronectin, or J1/tenascin as substrates was inhibited by addition of soluble J1/tenascin to the cultures. Neither of the two mAbs neutralized the neurite outgrowth-inhibitory properties of soluble J1/tenascin. In contrast to their opposite effects on neurite outgrowth, both substrate-bound and soluble J1/tenascin reduced spreading of the neuronal cell bodies, suggesting that the neurite outgrowth-promoting and antispreading effects are mediated by two different sites on the molecule. This was further supported by the inability of the mAb J1/tn2 to neutralize the antispreading effect. The J1/tn2 epitope localizes to a fibronectin type III homology domain that is presumably distinct from the putative Tn68 cell-binding domain of chicken tenascin for fibroblasts, as shown by electronmicroscopic localization of antibody binding sites. We infer from these experiments that J1/tenascin contains a neurite outgrowth promoting domain that is distinguishable from the cell-binding site and presumably not involved in the inhibition of neurite outgrowth or cell spreading. Our observations support the notion that J1/tenascin is a multifunctional extracellular matrix molecule.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Antibodies, Monoclonal
  • Axons / drug effects
  • Axons / physiology*
  • Axons / ultrastructure
  • Binding Sites, Antibody
  • Cell Adhesion / drug effects
  • Cell Adhesion Molecules, Neuronal / pharmacology*
  • Cells, Cultured
  • Embryo, Mammalian
  • Epitopes / analysis
  • Extracellular Matrix / physiology
  • Extracellular Matrix Proteins / pharmacology*
  • Hippocampus / physiology*
  • Hippocampus / ultrastructure
  • Kinetics
  • Mesencephalon / physiology*
  • Mesencephalon / ultrastructure
  • Microscopy, Electron
  • Neurons / drug effects
  • Neurons / physiology*
  • Neurons / ultrastructure
  • Rats
  • Tenascin

Substances

  • Antibodies, Monoclonal
  • Cell Adhesion Molecules, Neuronal
  • Epitopes
  • Extracellular Matrix Proteins
  • Tenascin