Generation of foxn1/Casper Mutant Zebrafish for Allograft and Xenograft of Normal and Malignant Cells

Stem Cell Reports. 2020 Sep 8;15(3):749-760. doi: 10.1016/j.stemcr.2020.07.020. Epub 2020 Aug 20.

Abstract

Cell transplantation into immunodeficient recipients is a widely used approach to study stem cell and cancer biology; however, studying cell states post transplantation in vivo is inconvenient in mammals. Here, we generated a foxn1/Casper mutant zebrafish that is transparent and exhibits T cell deficiency. By employing the line for hematopoietic stem cell (HSC) transplantation (HSCT), we could achieve nonconditioned transplantation. Meanwhile, we found that fetal HSCs from 3 days post fertilization zebrafish embryos produce a better transplant outcome in foxn1/Casper mutants, compared with adult HSCs. In addition to HSCT, the foxn1/Casper mutant is feasible for allografts of myelodysplastic syndrome-like and muscle cells, as well as xenografts of medaka muscle cells. In summary, foxn1/Casper mutants permit the nonconditioned engraftment of multiple cell types and visualized characterization of transplanted cells in vivo.

Keywords: foxn1/Casper mutant; hematopoietic stem cells; nonconditioned cell transplantation; xenograft; zebrafish.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Allografts / transplantation*
  • Animals
  • Base Sequence
  • Fetal Stem Cells / cytology
  • Forkhead Transcription Factors / genetics*
  • Forkhead Transcription Factors / metabolism
  • Hematopoietic Stem Cell Transplantation
  • Hematopoietic Stem Cells / cytology
  • Heterografts / transplantation*
  • Mutation / genetics*
  • Neoplasms / pathology*
  • Treatment Outcome
  • Zebrafish / embryology
  • Zebrafish / genetics*
  • Zebrafish Proteins / genetics*
  • Zebrafish Proteins / metabolism

Substances

  • Forkhead Transcription Factors
  • Foxn1 protein, zebrafish
  • Zebrafish Proteins