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Genetic Lineage Tracing of Non-cardiomyocytes in Mice.
Chen, Zhongming; van Berlo, Jop H.
Affiliation
  • Chen Z; Department of Medicine, Cardiovascular Division, Lillehei Heart Institute, University of Minnesota, Minneapolis, MN, USA.
  • van Berlo JH; Department of Medicine, Cardiovascular Division, Lillehei Heart Institute, University of Minnesota, Minneapolis, MN, USA. jvanberl@umn.edu.
Methods Mol Biol ; 2158: 323-336, 2021.
Article in En | MEDLINE | ID: mdl-32857384
ABSTRACT
Genetic lineage tracing is accomplished using bi-transgenic mice, where one allele is altered to express Cre recombinase, and another allele encodes a Cre-dependent genetic reporter protein. Once Cre is activated (constitutive or in response to tamoxifen), the marker gene-expressing cells become indelibly labeled by the reporter protein. Therefore, daughter cells derived from labeled cells are permanently labeled even if the marker gene that drove Cre recombinase expression is no longer expressed in these cells. This system is commonly used to label putative progenitor cells and determine the fate of their progeny. Here, we describe the use of c-kit-based genetic lineage-tracing mouse line as an example and discuss caveats for performing these types of experiments.
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Stem Cells / Cell Lineage / Cell Tracking Type of study: Prognostic_studies Limits: Animals Language: En Journal: Methods Mol Biol Journal subject: BIOLOGIA MOLECULAR Year: 2021 Document type: Article Affiliation country: United States

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Stem Cells / Cell Lineage / Cell Tracking Type of study: Prognostic_studies Limits: Animals Language: En Journal: Methods Mol Biol Journal subject: BIOLOGIA MOLECULAR Year: 2021 Document type: Article Affiliation country: United States