A Novel Mouse Model of iNKT Cell-deficiency Generated by CRISPR/Cas9 Reveals a Pathogenic Role of iNKT Cells in Metabolic Disease

Sci Rep. 2017 Oct 6;7(1):12765. doi: 10.1038/s41598-017-12475-4.

Abstract

iNKT cells play important roles in immune regulation by bridging the innate and acquired immune systems. The functions of iNKT cells have been investigated in mice lacking the Traj18 gene segment that were generated by traditional embryonic stem cell technology, but these animals contain a biased T cell receptor (TCR) repertoire that might affect immune responses. To circumvent this confounding factor, we have generated a new strain of iNKT cell-deficient mice by deleting the Traj18 locus using CRISPR/Cas9 technology, and these animals contain an unbiased TCR repertoire. We employed these mice to investigate the contribution of iNKT cells to metabolic disease and found a pathogenic role of these cells in obesity-associated insulin-resistance. The new Traj18-deficient mouse strain will assist in studies of iNKT cell biology.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • CRISPR-Associated Protein 9 / metabolism*
  • CRISPR-Cas Systems / genetics*
  • Diet, High-Fat
  • Disease Models, Animal
  • Genetic Loci
  • Glucose Intolerance / pathology
  • HEK293 Cells
  • Humans
  • Insulin Resistance
  • Metabolic Diseases / immunology*
  • Metabolic Diseases / pathology
  • Mice, Inbred BALB C
  • Mice, Inbred C57BL
  • Mutation / genetics
  • Natural Killer T-Cells / immunology*
  • Obesity / pathology
  • RNA, Guide, CRISPR-Cas Systems / metabolism
  • Receptors, Antigen, T-Cell, alpha-beta / genetics
  • Receptors, Antigen, T-Cell, alpha-beta / metabolism

Substances

  • RNA, Guide, CRISPR-Cas Systems
  • Receptors, Antigen, T-Cell, alpha-beta
  • CRISPR-Associated Protein 9