Genetic dissection of clonal lineage relationships with hydroxytamoxifen liposomes

Nat Commun. 2018 Jul 30;9(1):2971. doi: 10.1038/s41467-018-05436-6.

Abstract

Targeted genetic dissection of tissues to identify precise cell populations has vast biological and therapeutic applications. Here we develop an approach, through the packaging and delivery of 4-hydroxytamoxifen liposomes (LiTMX), that enables localized induction of CreERT2 recombinase in mice. Our method permits precise, in vivo, tissue-specific clonal analysis with both spatial and temporal control. This technology is effective using mice with both specific and ubiquitous Cre drivers in a variety of tissue types, under conditions of homeostasis and post-injury repair, and is highly efficient for lineage tracing and genetic analysis. This methodology is directly and immediately applicable to the developmental biology, stem cell biology and regenerative medicine, and cancer biology fields.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adipose Tissue / metabolism
  • Animals
  • Cartilage, Articular / metabolism
  • Cell Lineage*
  • Cells, Cultured
  • Chondrocytes / metabolism
  • Disease Models, Animal
  • Homeostasis
  • Injections, Intraperitoneal
  • Integrases / metabolism
  • Liposomes / chemistry*
  • Mice
  • Mice, Transgenic
  • Recombinases
  • Regenerative Medicine
  • Skin / metabolism
  • Stem Cells / cytology
  • Stem Cells / metabolism
  • Tamoxifen / analogs & derivatives*
  • Tamoxifen / chemistry
  • Wound Healing

Substances

  • Liposomes
  • Recombinases
  • Tamoxifen
  • afimoxifene
  • Cre recombinase
  • Integrases