Table 2

Phenotypic analysis of lck-ERT2-SCL tumors and derived cell lines

Primary tumor
Derived cell line
Animal no.Survival on TAM, moPredominant phenotypeNOTCH1+(%)Predominant phenotypeNOTCH1+%)NOTCH1 mutations
Fold change, quantitative RT-PCR
HDPESTNOTCH1
151 DN TCRβlow ND NA NA NA NA NA 
049 11 CD8 TCRβlow 86 CD8 TCRβlow 95 None None 3.3 
044 CD8 TCRβlow 61 CD8 TCRβlow 94 None 56676 C>CC* 6.7 
065 17 DP TCRβhigh 51 CD8 TCRβlow 86 None None 4.8 
Primary tumor
Derived cell line
Animal no.Survival on TAM, moPredominant phenotypeNOTCH1+(%)Predominant phenotypeNOTCH1+%)NOTCH1 mutations
Fold change, quantitative RT-PCR
HDPESTNOTCH1
151 DN TCRβlow ND NA NA NA NA NA 
049 11 CD8 TCRβlow 86 CD8 TCRβlow 95 None None 3.3 
044 CD8 TCRβlow 61 CD8 TCRβlow 94 None 56676 C>CC* 6.7 
065 17 DP TCRβhigh 51 CD8 TCRβlow 86 None None 4.8 

Thymic tumors of tamoxifen-treated lck-ERT2-SCL mice and corresponding cell lines were stained with antibodies against CD4, CD8, TCRβ, and NOTCH1 and analyzed by flow cytometry. Genomic DNA was isolated from the cell lines and NOTCH1 HD and PEST domain sequence analysis was performed. mRNA of the tumor cell lines was isolated, and quantitative RT-PCR was performed for NOTCH1. Fold change data represent change compared with normal wild-type FVB/N thymocytes.

TAM indicates tamoxifen; DN, double-negative; ND, not determined; NA, not applicable; and DP, double-positive.

*

Heterozygous mutation.

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