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Comparison of immunophenotypes between Rag2 knockout mice derived from two different sources.

Yu Jeong Roh1, Jeong Eun Gong1, Ji Eun Kim1

  • 1Department of Biomaterials Science (BK21 FOUR Program)/Life and Industry Convergence Research Institute/Laboratory Animal Resources Center, College of Natural Resources and Life Science, Pusan National University, Miryang, 50463, Korea.

Laboratory Animal Research
|January 10, 2023
PubMed
Summary

Recombination activating gene2 (Rag2) knockout mice from different sources show similar spleen and thymus changes. However, Rag2/Korl and Rag2/J KO mice exhibit distinct CD8+ T and B cell subpopulation counts.

Keywords:
B cellsImmunophenotypesKnockout miceRag2SpleenT cellsThymus

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Area of Science:

  • Immunology
  • Genetics
  • Animal Models

Background:

  • Recombination activating gene2 (Rag2) knockout (KO) mice are crucial research tools in immunology, vaccine development, and transplantation.
  • Phenotypic variations among Rag2 KO mice from different sources are not well-documented.
  • This study addresses the need for comparative analysis of Rag2 KO mouse immunophenotypes.

Purpose of the Study:

  • To investigate and compare the immunophenotypes of Rag2 KO mice from distinct genetic backgrounds.
  • To identify potential differences in spleen and thymus characteristics between C57BL/6-Rag2em1hwl/Korl (Rag2/Korl KO) and B6.Cg-Rag2tm1.1Cgn/J (Rag2/J KO) mice.
  • To evaluate organ weight, histological structure, and immune cell subpopulations.

Main Methods:

  • Comparative analysis of organ weights (spleen, thymus) between Rag2 KO and wild-type (WT) mice.
  • Histological examination of spleen and thymus tissues.
  • Flow cytometry to quantify immune cell subpopulations, including CD4+ T cells, CD8+ T cells, and B cells.

Main Results:

  • Both Rag2/Korl KO and Rag2/J KO mice exhibited reduced spleen and thymus weights compared to WT mice.
  • Histological analysis revealed decreased white pulp in the spleen and cortex in the thymus of both Rag2 KO groups.
  • Significant differences were observed in CD8+ T and B cell counts between Rag2/Korl KO and Rag2/J KO mice, while CD4+ T cell counts remained similar.

Conclusions:

  • Rag2/Korl KO and Rag2/J KO mice display largely similar immunophenotypes in spleen and thymus.
  • Key differences lie in the specific counts of CD8+ T and B cell subpopulations between these two Rag2 KO mouse models.
  • These findings highlight the importance of source-specific characterization of KO mouse models for research reproducibility.