FGF-2-responsive neural stem cell proliferation requires CCg, a novel autocrine/paracrine cofactor

Philippe Taupin, Jasodhara Ray, Wolfgang H. Fischer, Steven T. Suhr, Katarina Hakansson, Anders Grubb, Fred H. Gage

Research output: Contribution to journalArticlepeer-review

Abstract

We have purified and characterized a factor, from the conditioned medium of neural stem cell cultures, which is required for fibroblast growth factor 2's (FGF-2) mitogenic activity on neural stem cells. This autocrine/paracrine cofactor is a glycosylated form of cystatin C (CCg), whose N-glycosylation is required for its activity. We further demonstrated that, both in vitro and in vivo, neural stem cells undergoing cell division are immunopositive for cystatin C. Finally, we showed in vivo functional activity of CCg by demonstrating that the combined delivery of FGF-2 and CCg to the adult dentate gyrus stimulated neurogenesis. We propose that the process of neurogenesis is controlled by the cooperation between trophic factors and autocrine/paracrine cofactors, of which CCg is a prototype.

Original languageEnglish
Pages (from-to)385-97
JournalNeuron
Volume28
Issue number2
DOIs
Publication statusPublished - 2000
Externally publishedYes

Free keywords

  • Animals
  • Autocrine Communication/drug effects
  • Cell Division/drug effects
  • Cells, Cultured
  • Culture Media, Conditioned/chemistry
  • Cystatin C
  • Cystatins/chemistry
  • Dentate Gyrus/cytology
  • Fibroblast Growth Factor 2/genetics
  • Glycosylation
  • Hippocampus/cytology
  • Molecular Sequence Data
  • Molecular Weight
  • Neurons/cytology
  • Paracrine Communication/drug effects
  • Protein Processing, Post-Translational
  • Rats
  • Sequence Analysis, Protein
  • Stem Cell Transplantation
  • Stem Cells/cytology

Fingerprint

Dive into the research topics of 'FGF-2-responsive neural stem cell proliferation requires CCg, a novel autocrine/paracrine cofactor'. Together they form a unique fingerprint.

Cite this