Basic Information
Description
The mouse Tnfr2 gene was replaced by human TNFR2 coding sequence in B-hTNFR2 MC38 cells. Human TNFR2 is highly expressed on the surface of B-hTNFR2 MC38 cells.
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Targeting strategy
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The exogenous promoter and human TNFR2 coding sequence was inserted to replace the extracellular region of the mouse. The insertion disrupts the endogenous murine Tnfr2 gene, resulting in a non-functional transcript.
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Protein expression analysis
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TNFR2 expression analysis in B-hTNFR2 MC38 cells by flow cytometry. Single cell suspensions from wild-type MC38 and B-hTNFR2 MC38 cultures were stained with species-specific anti-TNFR2 antibody. Mouse TNFR2 was detected on the surface of wild-type MC38 cells. Human TNFR2 was detected on the surface of B-hTNFR2 MC38 cells but not wild-type MC38 cells. The 6-D05 clone of B-hTNFR2 MC38 cells was used for in vivo experiments.
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Tumor growth curve
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Subcutaneous homograft tumor growth of B-hTNFR2 MC38 cells. B-hTNFR2 MC38 cells (5×105) and wild-type MC38 cells (5×105) were subcutaneously implanted into C57BL/6N mice (female, 6-9-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-hTNFR2 MC38 cells were able to establish tumors in vivo and can be used for efficacy studies.
