Endothelial-Specific Cre Mouse Models

Arterioscler Thromb Vasc Biol. 2018 Nov;38(11):2550-2561. doi: 10.1161/ATVBAHA.118.309669.

Abstract

The field of vascular biology has gained enormous insight from the use of Cre and inducible Cre mouse models to temporally and spatially manipulate gene expression within the endothelium. Models are available to constitutively or inducibly modulate gene expression in all or a specified subset of endothelial cells. However, caution should be applied to both the selection of allele and the analysis of resultant phenotype: many similarly named Cre models have divergent activity patterns while ectopic or inconsistent Cre or inducible Cre expression can dramatically affect results. In an effort to disambiguate previous data and to provide a resource to aid appropriate experimental design, here we summarize what is known about Cre recombinase activity in the most widely used endothelial-specific Cre and Cre/ERT2 mouse models.

Keywords: endothelial cells; gene expression; mice; phenotype; recombinases.

Publication types

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

MeSH terms

  • Animals
  • Cardiovascular Diseases / genetics
  • Cardiovascular Diseases / metabolism
  • Cardiovascular Diseases / pathology
  • Disease Models, Animal
  • Endothelial Cells / drug effects
  • Endothelial Cells / metabolism*
  • Endothelial Cells / pathology
  • Gene Expression Regulation / drug effects
  • Gene Targeting / methods*
  • Genotype
  • Integrases / genetics*
  • Integrases / metabolism
  • Mice, Transgenic
  • Phenotype
  • Protein Interaction Domains and Motifs / genetics
  • Receptors, Estrogen / drug effects
  • Receptors, Estrogen / genetics*
  • Receptors, Estrogen / metabolism
  • Selective Estrogen Receptor Modulators / pharmacology
  • Tamoxifen / pharmacology

Substances

  • Receptors, Estrogen
  • Selective Estrogen Receptor Modulators
  • Tamoxifen
  • Cre recombinase
  • Integrases