NSG mouse

NSG, or NOD scid gamma (NOD.Cg-Prkdc^scid Il2rg^tm1Wjl/SzJ), is a strain of inbred laboratory mice, among the most immunodeficient described to date.^[1] NSG mice lack mature T cells, B cells, and natural killer (NK) cells.^[2] NSG mice are also deficient in multiple cytokine signaling pathways, and they have many defects in innate immunity.^[2][3] The compound immunodeficiencies in NSG mice permit the engraftment of a wide range of primary human cells, and enable sophisticated modeling of many areas of human biology and disease. NSG mice were developed in the laboratory of Dr. Leonard Shultz at The Jackson Laboratory.

Features of NSG mice

• The genetic background, derived from inbred NOD mouse strain NOD/ShiLtJ, contributes reductions in innate immunity that include an absent hemolytic complement system, reduced dendritic cell function, and defective macrophage activity.^[3] The NOD/ShiLtJ background also contributes an allele of the Sirpa gene that renders the bone marrow niche very permissive to colonization by human hematopoietic stem cells.^[4]
• The Prkdc^scid mutation^a, commonly known as “scid” or “severe combined immunodeficiency”, essentially eliminates adaptive immunity.^[5] Prkdc^scid is a loss-of-function mutation in the mouse homologue of the human PRKDC gene, which encodes a protein that resolves DNA strand breaks that occur during V(D)J recombination in developing T and B lymphocytes.^[6] Mice homozygous for the mutation have severely reduced numbers of mature T and B cells.^[3][5] The phenotypic penetrance of Prkdc^scid varies among inbred strain backgrounds, but the mutation is most effective at eliminating adaptive immunity on the NOD genetic background.^[3]
• The Il2rg^tm1Wjl targeted mutation^b is a complete null mutation in the gene encoding the interleukin 2 receptor gamma chain (IL2Rγ, homologous to IL2RG in humans).^[7] IL2Rγ is a common component of the cell surface receptors that bind and transduce signals from six distinct interleukins. Signaling through IL2Rγ is required for the differentiation and function of many hematopoietic cells.^[7] Notably, the absence of IL2Rγ blocks NK cell differentiation, and thereby removes a major obstacle preventing the efficient engraftment of primary human cells.^[2][5]

Research applications of NSG include

• Primary human lung tumor xenografts that preserve the tumor microenvironment during long-term engraftment ^[8]
• Humanized model for evaluation of possible cancer curing gene therapy. ^[9]
• Models of acute or chronic leukemia established using cancer cells collected from patients (A complete list of publications is available here)
• A highly sensitive platform for studying epithelial ^[10] and cancer stem cells ^[11]
• Establishing a functional, humanized immune system from engrafted human hematopoietic stem cells ^[12][13] and progenitors ^[14]
• Humanized models for studying human-specific infectious diseases like HIV,^[15] Epstein Barr virus,^[16] malaria,^[17] and Dengue fever.^[18][19] Humanized models also aid in testing new therapies ^[15]
• Studying allograft rejection after pancreatic islet transplantation therapy for type 1 diabetes ^[20]

References

Notes

1.^ Mouse Genome Informatics entry for Prkdc^scid

2.^ Mouse Genome Informatics entry for Il2rg^tm1Wjl

External links

• NSG strain datasheet at The Jackson Laboratory
• NSG discussion forum
• Categorized list of references