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Vascular Biology - COBRE

Interdisciplinary Research in Vascular Biology

Interdisciplinary Research in Vascular Biology Center of Biomedical Research Excellence (COBRE)

  • Welcome
  • Administrative Core
    • Internal Steering Committee
    • External Advisory Committee
    • Mentoring
  • Pilot Project Core
  • Microscopy Core
  • Phenotyping Core
    • Equipment
    • Mouse Genetic Resources for Vascular Studies

Mouse Genetic Resources for Vascular Studies

Inducible or tissue-specific gene deletion or in vivo labeling of gene expression have become major research approaches for accurate assessment of complex cardiovascular phenotypes in mice. This approach requires crossing mice with the targeted gene of interest with a validated specific Cre or reporter mouse line. However, developing and obtaining these unique mouse genetic tools is often time consuming and expensive. Over the past 10 years, the COBRE has collected and characterized 19 tissue-specific Cre lines, 5 reporter lines, and 4 commonly used vascular disease lines and mouse strains (Table). To reduce the cost of breeding and accelerate the breeding process, the Core has established a centralized system to maintain breeding pairs of these valuable lines, which are available to COBRE or non-COBRE investigators upon request (2 months in advance to allow breeding). The Core has also established a relationship with a gene-targeting company to provide rapid, competitively priced genetically engineered mice.

 

Inducible or tissue specific Cre lines Reporter lines and other mouse genetic lines
  • Cdh5-CreERT2 (inducible Cre in endothelial cells) from Dr. Ralf Adams.
  • Tie2-Cre (endothelial and hematopoietic cells) from Dr. Masashi Yanagisawa.
  • Prox1-CreERT2 (prox1+ cells including lymphatic ECs) from Dr. Guillermo Oliver.
  • VE-Cadherin-Cre (endothelial cells) from Dr. Iruela-Arispe.
  • Pdgfrβ-Cre (stromal and smooth muscle cells) from Dr. Ralf Adams.
  • Lyve1-Cre (lymphatic endothelium).
  • SM22-Cre (vascular smooth muscle).
  • Pf4-Cre (megakaryocytes and platelets).
  • LysM-Cre (myeloid cells).
  • Cag-CreERT2 (global inducible Cre).
  • Villin-Cre (intestinal epithelial cells).
  • UBC-CreER (ubiquitous CreER).
  • Tagln-Cre (smooth muscle)
  • Myh11-CreER (very specific smooth muscle CreER)
  • Adiponectin-Cre (mature adipocytes).
  • Nestin-Cre (neural cells, pericytes, muscle).
  • Ng2-Cre (nervous system, adipose tissue, pericytes)
  • Ng2-CreER (nervous system, adipose tissue, pericytes).
  • Myf5-Cre (knockin line, skeletal muscle, brown fat).
  • Tie2GFP (endothelial specific).
  • LysM-eGFP (myeloid cells)
  • R26-mTomato/mEGFP (constitutively global red until Cre recombination turns it green in specific cell types).
  • R26-tdTomato-WPRE (global expression, very bright red).
  • R26-Neo/lacZ/EGFP (Cre turns on nuclear lacZ, then Flp turns on green).
  • ApoE-/- (atherosclerosis prone model).
  • Ldlr-/- (atherosclerosis prone model).
  • SJL/J (for transplant studies)
  • C57BL/6J (available for controls)
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  • Welcome
  • Administrative Core
    • Internal Steering Committee
    • External Advisory Committee
    • Mentoring
  • Pilot Project Core
  • Microscopy Core
  • Phenotyping Core
    • Equipment
    • Mouse Genetic Resources for Vascular Studies