Tamoxifen-inducible glia-specific Cre mice for somatic mutagenesis in oligodendrocytes and Schwann cells

Mol Cell Neurosci. 2003 Apr;22(4):430-40. doi: 10.1016/s1044-7431(03)00029-0.

Abstract

Inducible transgenesis provides a valuable technique for the analysis of gene function in vivo. We report the generation and characterization of mouse lines carrying glia lineage-specific transgenes expressing an improved variant of the tamoxifen-inducible Cre recombinase, CreERT2, where the recombinase is fused to a mutated ligand binding domain of the human estrogen receptor. Using a PLP-CreERT2 transgene, we have generated mice that show specific inducible Cre function, as analyzed by cross-breeding experiments into the Rosa26 Cre-LacZ reporter line, in developing and adult Schwann cells, in mature myelinating oligodendrocytes, and in undifferentiated NG2-positive oligodendrocyte precursors in the adult. Using a P0Cx-CreERT2 transgene, we have also established mouse lines with inducible Cre function specifically in the Schwann cell lineage. These tamoxifen-inducible CreERT2 lines will allow detailed spatiotemporally controlled analysis of gene functions in loxP-based conditional mutant mice in both developing and adult Schwann cells and in the oligodendrocyte lineage.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Animals, Newborn
  • Brain / cytology
  • Brain / drug effects
  • Brain / growth & development
  • Cell Lineage / genetics
  • Dose-Response Relationship, Drug
  • Female
  • Fetus
  • Gene Expression Regulation / genetics*
  • Genes, Reporter / genetics
  • Integrases / genetics*
  • Lactation / drug effects
  • Male
  • Mice
  • Mice, Transgenic
  • Mutagenesis / drug effects
  • Mutagenesis / genetics*
  • Oligodendroglia / drug effects
  • Oligodendroglia / metabolism*
  • Peripheral Nervous System / cytology
  • Peripheral Nervous System / drug effects
  • Peripheral Nervous System / growth & development
  • Protein Structure, Tertiary / genetics
  • Receptors, Estrogen / genetics
  • Recombinant Fusion Proteins
  • Schwann Cells / drug effects
  • Schwann Cells / metabolism*
  • Stem Cells / cytology
  • Stem Cells / metabolism
  • Tamoxifen / pharmacology*
  • Transgenes / drug effects
  • Transgenes / genetics*
  • Viral Proteins / genetics*

Substances

  • Receptors, Estrogen
  • Recombinant Fusion Proteins
  • Viral Proteins
  • Tamoxifen
  • Cre recombinase
  • Integrases