Genetically modified mice expressing humanized CD47
The present disclosure relates to genetically modified non-human animals that express a human or chimeric (e.g., humanized) CD47, and methods of use thereof.
1. A genetically modified mouse whose genome comprises a nucleic acid sequence encoding a chimeric CD47 comprising a humanized extracellular region and five endogenous transmembrane domains, wherein the nucleic acid sequence is operably linked to an endogenous CD47 promoter and the mouse functionally expresses the chimeric CD47.
2. The genetically modified mouse of claim 1 , wherein the mouse does not express endogenous CD47.
3. The genetically modified mouse of claim 1 , wherein the mouse is homozygous with respect to the nucleic acid sequence encoding the chimeric CD47.
4. The genetically modified mouse of claim 1 , wherein the genome of the mouse further comprises a nucleic acid sequence encoding a humanized SIRPα.
5. A method of evaluating a drug for treating a tumor, the method comprising:
a) administering the drug to the genetically modified mouse of claim 1 , wherein the mouse has a tumor comprising human cancer cells; and
b) determining whether the drug inhibits the tumor.
6. The method of claim 5 , wherein the drug is an anti-CD47 antibody.
7. A genetically modified mouse whose genome comprises a chimeric CD47 gene comprising a replacement of a nucleic acid sequence encoding an extracellular domain within exon 2 of an endogenous CD47 gene with a nucleic acid sequence encoding an extracellular domain within exon 2 of a human CD47 gene, and endogenous exons 3-7, wherein the mouse functionally expresses a chimeric CD47.
8. The genetically modified mouse of claim 7 , wherein the mouse does not express endogenous CD47.
9. The genetically modified mouse of claim 7 , wherein the mouse is homozygous with respect to the nucleic acid sequence encoding the chimeric CD47.
10. The genetically modified mouse of claim 7 , wherein the genome of the mouse further comprises a nucleic acid sequence encoding a humanized SIRPα.
11. The genetically modified mouse of claim 7 , wherein the nucleic acid sequence encoding an extracellular domain within exon 2 of a human CD47 gene is at least 300 nucleotides.
12. A method of preparing a genetically modified mouse, the method comprising:
1) providing a plasmid comprising a human CD47 gene fragment from exon 2 of the human CD47 gene, a 5′ homology arm, and a 3′ homology arm, wherein the 5′ and 3′ homology arms target exon 2 of a mouse CD47 gene;
2) providing a first single guide RNA (sgRNA) that targets a nucleic acid sequence selected from the group consisting of SEQ ID NO: 1, SEQ ID NO: 2, SEQ ID NO: 3, SEQ ID NO: 4, SEQ ID NO: 5, SEQ ID NO: 6, SEQ ID NO: 7, and SEQ ID NO: 8;
3) providing a second sgRNA that targets a nucleic acid sequence selected from the group consisting of SEQ ID NO: 9, SEQ ID NO: 10, SEQ ID NO: 11, SEQ ID NO: 12, SEQ ID NO: 13, SEQ ID NO: 14, SEQ ID NO: 15, and SEQ ID NO: 16;
4) modifying the genome of a mouse embryo using the plasmid of step 1), the first sgRNA of step 2), the second sgRNA of step 3), and Cas9; and
5) transplanting the embryo obtained in step 4) into a recipient mouse such that a transgenic mouse is obtained whose genome comprises a nucleic acid sequence encoding a chimeric CD47 comprising a humanized extracellular region and five endogenous transmembrane domains, wherein the nucleic acid sequence is operably linked to an endogenous CD47 promoter and the mouse functionally expresses the chimeric CD47.
13. The genetically modified mouse of claim 12 , wherein the first sgRNA targets the nucleic acid sequence of SEQ ID NO: 6 and the second sgRNA targets the nucleic acid sequence of SEQ ID NO: 9.