top
Please input keywords
Order
*Country
한국
미국
일본
중국
영국
호주
프랑스
독일
이탈리아
싱가포르
인도
러시아
캐나다
스위스
기타 국가
*Province
*City
*Name
*Telephone
*Company
*Position
*Email
*Verification code
*Verification Code
B-hHLA-DRB1*7.1 mice
Strain Name

C57BL/6-H2-Eatm1(HLA-DRA1*1.1-I-Ea)Bcgen 

H2-Eb1tm1(HLA-DRB1*7.1-I-Eb1)Bcgen 

H2-Atm1Bcgen H2-Eb2tm1Bcgen/Bcgen

Common Name 

B-hHLA-DRB1*7.1 mice

Background C57BL/6 Catalog number 112948
Related Genes 

HLA-DRA1; SS1, DRB1, HLA-DRB, HLA-DR1B

NCBI Gene ID

3122, 3123

Description

  • HLA-DRA is one of the HLA class II alpha chain paralogues. HLA-DRB1 belongs to the HLA class II beta chain paralogs. This class II molecule is a heterodimer consisting of an alpha (DRA) and a beta (DRB) chain, both anchored in the membrane. It plays a central role in the immune system by presenting peptides derived from extracellular proteins. Class II molecules are expressed in antigen presenting cells (APC: B lymphocytes, dendritic cells, macrophages). The alpha chain is approximately 33-35 kDa and its gene contains 5 exons. The beta chain is approximately 26-28 kDa and its gene contains 6 exons. DRA does not have polymorphisms in the peptide binding part and acts as the sole alpha chain for DRB1, DRB3, DRB4 and DRB5.
  • The exon 2 of mouse I-Ea gene that encodes the extracellular domain of I-Ea was replaced by human HLA-DRA encoding the α1 domain in B-hHLA-DRB1*7.1 mice. The exon 2 of mouse I-Eb1 gene that encodes the extracellular domain of I-Eb1 was replaced by human HLA-DRB encoding the β1 domain in B-hHLA-DRB1*7.1 mice. The  mouse I-Aa, I-Ab1 and I-Eb2 were knocked out in B-hHLA-DRB1*7.1 mice.
  • Human HLA-DR was exclusively detectable in homozygous B-hHLA-DRB1*7.1 mice, but not in wild-type C57BL/6 mice.
  • B-hHLA-DRB1*7.1 mice provide a powerful preclinical model for in vivo evaluation of vaccines.
  • Application: For example, this product is used for pharmacodynamics and safety evaluation of vaccines for cancers.

Targeting strategy

Gene targeting strategy for B-hHLA-DRB1*7.1 mice. The exon 2 of mouse I-Ea gene that encodes the extracellular domain of I-Ea was replaced by human HLA-DRA encoding the α1 domain in B-hHLA-DRB1*7.1 mice. The exon 2 of mouse I-Eb1 gene that encodes the extracellular domain of I-Eb1 was replaced by human HLA-DRB encoding the β1 domain in B-hHLA-DRB1*7.1 mice. The  mouse I-Aa, I-Ab1 and I-Eb2 were knocked out in B-hHLA-DRB1*7.1 mice.

Protein expression analysis in spleen

from clipboard

Strain specific HLA-DR expression analysis in wild-type C57BL/6 mice and homozygous B-hHLA-DRB1*7.1 mice by flow cytometry. Spleen cells were collected from wild-type C57BL/6 mice (+/+) and homozygous humanized B-hHLA-DRB1*7.1 mice, respectively, and analyzed by flow cytometry with species-specific anti-mouse I-A/I-E antibody (Biolegend, 107607), and species-specific anti-human HLA-DR antibody (Biolegend, 307610). Human HLA-DR was exclusively detectable in homozygous B-hHLA-DRB1*7.1 mice, but not in wild-type C57BL/6 mice. 


Protein expression analysis in blood

from clipboardStrain specific HLA-DR expression analysis in wild-type C57BL/6 mice and homozygous B-hHLA-DRB1*7.1 mice by flow cytometry. Blood cells were collected from wild-type C57BL/6 mice (+/+) and homozygous humanized B-hHLA-DRB1*7.1 mice, respectively, and analyzed by flow cytometry with species-specific anti-mouse I-A/I-E antibody (Biolegend, 107607), and species-specific anti-human HLA-DR antibody (Biolegend, 307610). Human HLA-DR was exclusively detectable in homozygous B-hHLA-DRB1*7.1 mice, but not in wild-type C57BL/6 mice. 

Protein expression analysis in bone marrow

from clipboard

Strain specific HLA-DR expression analysis in wild-type C57BL/6 mice and homozygous B-hHLA-DRB1*7.1 mice by flow cytometry. Bone marrow was collected from wild-type C57BL/6 mice (+/+) and homozygous humanized B-hHLA-DRB1*7.1 mice, respectively, and analyzed by flow cytometry with species-specific anti-mouse I-A/I-E antibody (Biolegend, 107607), and species-specific anti-human HLA-DR antibody (Biolegend, 307610). Human HLA-DR was exclusively detectable in homozygous B-hHLA-DRB1*7.1 mice, but not in wild-type C57BL/6 mice. 

Frequency of leukocyte subpopulations in spleen

from clipboard

Frequency of leukocyte subpopulations in spleen by flow cytometry. Splenocytes were isolated from wild-type C57BL/6 mice and homozygous B-hHLA-DRB1*7.1 mice (Female,8-week-old, n=3). A. Flow cytometry analysis of the splenocytes was performed to assess the frequency of leukocyte subpopulations. B. Frequency of T cell subpopulations. Frequencies of T cells, B cells, NK cells, DCs, monocytes, macrophages, neutrophils, and Tregs in B-hHLA-DRB1*7.1 mice were similar to those in C57BL/6 mice. Percent of CD8+ T cells were significantly decreased while percent of CD4+ T cells were significantly increased, demonstrating that introduction of HLA-DRB1*7.1 in place of mouse H2-E may affected the development of CD4+ T and CD8+T cells, which in turn affected the proportion of T cell subtypes in the spleen. Values are expressed as mean ± SEM. 

Frequency of leukocyte subpopulations in blood

from clipboard


Frequency of leukocyte subpopulations in blood by flow cytometry. Blood cells were isolated from wild-type C57BL/6 mice and homozygous B-hHLA-DRB1*7.1 mice (Female,8-week-old, n=3). A. Flow cytometry analysis of the blood cells was performed to assess the frequency of leukocyte subpopulations. B. Frequency of T cell subpopulations. Frequencies of T cells, B cells, NK cells, DCs, monocytes, macrophages, neutrophils, CD4+ T cells, CD8+ T cells  and Tregs in B-hHLA-DRB1*7.1 mice were similar to those in C57BL/6 mice, demonstrating that humanization of HLA-DRB1*7.1 does not change the frequency or distribution of these cell types in blood.

Frequency of leukocyte subpopulations in lymph node

from clipboard

Frequency of leukocyte subpopulations in lymph node by flow cytometry. Lymph nodes were isolated from wild-type C57BL/6 mice and homozygous B-hHLA-DRB1*7.1 mice (Female,8-week-old, n=3). A. Flow cytometry analysis of the lymph nodes cells was performed to assess the frequency of leukocyte subpopulations. B. Frequency of T cell subpopulations. Frequencies of T cells, B cells, NK cells, DCs, monocytes, macrophages, neutrophils, CD4+ T cells, CD8+ T cells  and Tregs in B-hHLA-DRB1*7.1 mice were similar to those in C57BL/6 mice, demonstrating that humanization of HLA-DRB1*7.1 does not change the frequency or distribution of these cell types in lymph nodes.