Basic Information
Description
The mouse Pdl1 gene and Cd39 gene were replaced by human PD-L1 and CD39 coding sequence in B-hPD-L1/hCD39 MC38 cells. Human PD-L1 and CD39 are highly expressed on the surface of B-hPD-L1/hCD39 MC38 cells.
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Targeting strategy
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Gene targeting strategy for B-hPD-L1/hCD39 MC38 cells. The exogenous promoter and human PD-L1 coding sequence was inserted to replace part of murine exon 3. The insertion disrupts the endogenous murine Pdl1 gene, resulting in a non-functional transcript. The exogenous promoter and human CD39 coding sequence were inserted into the targeting vector used in the lentivirus system.
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Protein expression analysis
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PD-L1 and CD39 expression analysis in B-hPD-L1/hCD39 MC38 cells by flow cytometry. Single cell suspensions from wild-type MC38 and B-hPD-L1/hCD39 MC38 cultures were stained with species-specific anti-PD-L1 and anti-CD39 antibody. Human PD-L1 and CD39 were detected on the surface of B-hPD-L1/hCD39 MC38 cells but not wild-type MC38 cells. The 3-A09 clone of B-hPD-L1/hCD39 MC38 cells was used for in vivo experiments. -
Tumor growth curve & Body weight changes
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Subcutaneous homograft tumor growth of B-hPD-L1/hCD39 MC38 cells. B-hPD-L1/hCD39 MC38 cells (5×105, 1×106) and wild-type MC38 cells (5×105) were subcutaneously implanted into B-hPD-1/hCD39 mice (female, 8-week-old, n=8). 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-hPD-L1/hCD39 MC38 cells were able to establish tumors in vivo and can be used for efficacy studies.
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Protein expression analysis of tumor cells
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B-hPD-L1/hCD39 MC38 cells were subcutaneously transplanted into B-hPD-1/hCD39 mice (n=8), and on 39 days post inoculation, tumor cells were harvested and assessed for human PD-L1 and CD39 expression by flow cytometry. As shown, human PD-L1 and CD39 were highly expressed on the surface of tumor cells. Therefore, B-hPD-L1/hCD39 MC38 cells can be used for in vivo efficacy studies of novel PD-L1 and CD39 therapeutics.
