hCRBN

Background : C57BL/6Smoc

Catalog : NM-HU-225071

Strain Name : C57BL/6Smoc-Crbntm1(hCRBN)Smoc

Gene Summary

Gene Name
  • Synonyms :

    piL, AF229032, AW108261, 2610203G15Rik, 2900045O07Rik

  • NCBI ID :

    58799

  • MGI ID :

    1913277

  • Ensembl ID :

    ENSMUSG00000005362

  • Strain State :

    活体

Model Description

The endogenous mouse Crbn gene was replaced by human CRBN gene.

Validation Data

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Fig.1 Detection of CRBN expression in spleen, brain, liver, intestine and muscle tissues by RT-PCR. 

Wild type: only one band at 185 bp with primers F1/R1 (mCrbn);

Homozygous: one band at 262 bp with primers F2/R2 (hCRBN) and one band at 374 bp with primers F3/R3 (hCRBN);

Abbr. M, DNA marker; HO, homozygous;  WT, wild type.

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Fig.2 Expression characterization of hCRBN in homozygous hCRBN KI mice by Western blot.

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Fig. 3 The degradation of GSPT1, CK1a and Myc by Lenalidomide and CC-885 in hCRBN knockin mice were determined by western blot.

The splenocytes derived from wild-type C57BL/6 (WT) and homozygous hCRBN KI (HO) mice were treated with 1% DMSO, Lenalidomide (10 nM, 100 nM, 1000 nM) and CC-885 (10 nM, 100 nM, 1000 nM) ,respectively, in RPMI-1640 cell culture medium for 18 hours ex vivo.

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Fig.4 Blood concentration curves of Lenalidomidein in C57BL/6 and HO hCRBN mice (female, 10wks, n=3).

(In cooperation with a client)

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Fig.5 Blood concentration of CC-885 in C57BL/6 and  hCRBN mice 1h after first administration (female, 10wks). (In cooperation with a client)

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Fig.6 Mean body weight (A) and survival curve (B) of C57BL/6 and HO hCRBN KI mice treated with CC-885 or vehicle (n=8/group). 

All hCRBN mice treated with CC-885 dead within 2 days, while mice from other groups survived. The result indicates that CC-885 exhibits significant toxicity only in hCRBN humanized mice (In cooperation with a client).

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Fig.7 The degradation of GSPT1, CK1a and Myc by CC-885 in C57BL/6 and hom hCRBN knockin mice in vivo (In cooperation with a client).

The wild-type C57BL/6 (WT, group 1&2) and homozygous hCRBN KI (HO, group 3&4) mice were treated with vehicle (group 1&3)  and 5 mg/kg CC-885 (group 2&4) , respectively. The mice were anesthetized, perfused, and tissues were harvested at 6 hr post the 2nd administration.

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Fig.8 Partial representative pictures of small intestine pathology (Magnification: 200x).

(In cooperation with a client)

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Fig.9 Partial representative pictures of liver pathology (Magnification: 200x).

(In cooperation with a client)

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Fig.10 Partial representative pictures of spleen pathology (Magnification: 200x).

(In cooperation with a client)

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