The mouse Cxcr2 gene was replaced by human CXCR2 coding sequence in B-hCXCR2 MC38 cells. Human CXCR2 is highly expressed on the surface of B-hCXCR2 MC38 cells.

Gene targeting strategy for B-hCXCR2 MC38 cells. The exogenous promoter and human CXCR2 coding sequence were inserted to replace part of murine exon 2 ~ 3’UTR. The insertion disrupts the endogenous murine Cxcr2 gene, resulting in a non-functional transcript.

CXCR2 expression analysis in B-hCXCR2 MC38 cells by flow cytometry. Single cell suspensions from wild-type MC38 and B-hCXCR2 MC38 cultures were stained with species-specific anti-CXCR2 antibody. Human CXCR2 was detected on the surface of B-hCXCR2 MC38 cells, but not on the surface of wild-type MC38 cells. The 6-F02 clone of B-hCXCR2 MC38 cells was used for in vivo experiments.

Subcutaneous homograft homograft tumor growth of B-hCXCR2 MC38 cells. B-hCXCR2 MC38 cells (5x10⁵) and wild-type MC38 cells (5x10⁵) were subcutaneously implanted into C57BL/6N mice (female, 7-week-old, n=5). Tumor volume and body weight were measured twice a week. (A) Average tumor volume ± SEM. (B) Body weight (Mean ± SEM). Volume was expressed in mm³ using the formula: V=0.5 X long diameter X short diameter². As shown in panel A, B-hCXCR2 MC38 cells were able to establish tumors in vivo and can be used for efficacy studies.

B-hCXCR2 MC38 tumor growth of individual mice. B-hCXCR2 MC38 cells (5x10⁵) and wild-type MC38 cells (5x10⁵) were subcutaneously implanted into C57BL/6N mice (female, 7-week-old, n=5). As shown in panel, B-hCXCR2 MC38 cells were able to establish tumors in vivo and can be used for efficacy studies.