C57BL/6-Tfrctm1(TFRC)Bcgen Slc3a2tm1(SLC3A2)Bcgen Igf1rtm5(IGF1R)Bcgen/Bcgen • 114637
TFR1: Target for Drug Delivery Across the BBB
TFR1:
The exons 4 19 of mouse Tfr1 gene that encode extracellular domain are replaced by human counterparts.
The genomic region of mouse Tfr1 gene that encodes cytoplasmic portion is retained. The promoter, 5’UTR and 3’UTR region of the mouse gene are also retained.
The chimeric TFR1 expression is driven by endogenous mouse Tfr1 promoter, while mouse Tfr1 gene transcription and translation will be disrupted.
CD98HC:
The exons 2 10 of mouse CD98HC gene that encode extracellular domain are replaced by human CD98HC exons 4 12.
The genomic region of mouse CD98HC gene that encodes cytoplasmic portion is retained. The promoter, 5’UTR and 3’UTR region of the mouse gene are also retained.
The chimeric CD98HC expression is driven by endogenous mouse CD98HC promoter, while mouse CD98HC gene transcription and translation will be disrupted.
IGF1R:
A chimeric CDS that encodes mouse Igf1r signal peptide and human extracellular domain, human transmembrane and mouse cytoplasmic domain, as well as mouse 3’UTR regionwere inserted right after mouse Igf1r exon 2 to replace the exon 2 of mouse Igf1r gene.
The chimeric IGF1R protein expression will be driven by endogenous mouse Igf1r promoter, while mouse Igf1r gene transcription and translation will be disrupted.
B-hTFR1/hCD98HC/hIGF1R plus mice were obtained by mating B-hTFR1 mice (110861), B-hCD98HC mice (110983) and B-hIGF1R mice plus (111974).
Strain-specific TFR1, CD98HC and IGF1R expression analysis in wild-type C57BL/6JNifdc mice, homozygous B-hCD98HC/hIGF1R plus mice and homozygousB-hTFR1/hCD98HC/hIGF1R plus mice. Cortex lysates were collected from wild-type C57BL/6JNifdc mice (+/+), homozygous B-hCD98HC/hIGF1R plus mice andhomozygous B-hTFR1/hCD98HC/hIGF1R plus mice, and then analyzed by western blot with anti-transferrin receptor antibody (abcam, ab214039), anti-CD98antibody (abcam, ab307587) and anti-IGF1R antibody (CST, 3027). 30 μg total proteins were loaded for western blotting analysis.