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C57BL/6JCya-Vdrem1/Cya
Common Name:
Vdr-KO
Product ID:
S-KO-15778
Background:
C57BL/6JCya
Product Type
Age
Genotype
Sex
Quantity
Price:
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Basic Information
Strain Name
Vdr-KO
Strain ID
KOCMP-22337-Vdr-B6J-VB
Gene Name
Vdr
Product ID
S-KO-15778
Gene Alias
Nr1i1
Background
C57BL/6JCya
NCBI ID
22337
Modification
Conventional knockout
Chromosome
15
Phenotype
MGI:103076
Document
Click here to download >>
Application
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Note
Note: When using this mouse strain in a publication, please cite “C57BL/6JCya-Vdrem1/Cya mice (Catalog S-KO-15778) were purchased from Cyagen.”
Strain Description
Ensembl Number
ENSMUST00000023119
NCBI RefSeq
NM_009504
Target Region
Exon 4
Size of Effective Region
~1.4 kb
Detailed Document
Click here to download >>
Overview of Gene Research
Vdr, short for Vitamin D receptor, is a nuclear receptor that plays a crucial role in mediating the biological functions of 1α,25-dihydroxyvitamin D3. It is essential for the regulation of intestinal cell proliferation, barrier function, and immunity, and is involved in various pathways such as the regulation of innate and adaptive immune responses [2,3,4]. Genetic models, like gene knockout mice, have been valuable in studying its functions.

In a VDR gene knockout mouse model (VDR-/ -), when combined with a murine model of cardiac steatosis expressing DGAT1 in cardiac myocytes, there was an amplification of lipotoxic cardiomyopathy. The double-modified mice showed increased myocyte size, heart weight/body weight ratio, natriuretic peptide gene expression, interstitial fibrosis, and up-regulation of related genes, along with significant reduction in ejection fraction and fractional shortening, suggesting that VDR deficiency enhances the pathological phenotype in this cardiomyopathy model [5]. Also, in vitro studies using VDR siRNA in HK-2 cells under high glucose/transforming growth factor beta stimulation demonstrated that VDR siRNA negated the activating effects of paricalcitol on mitochondrial function, indicating VDR's role in maintaining mitochondrial function in renal tubular cells [1].

In conclusion, Vdr is a key regulator in multiple biological processes. The use of Vdr KO mouse models has revealed its importance in diseases such as cardiomyopathy and in maintaining mitochondrial function in renal tubular cells, providing insights into the underlying mechanisms and potential therapeutic targets for these disease areas.

References:

1. Chen, Hong, Zhang, Hao, Li, Ai-Mei, Zhan, Ming, Yang, Shikun. 2024. VDR regulates mitochondrial function as a protective mechanism against renal tubular cell injury in diabetic rats. In Redox biology, 70, 103062. doi:10.1016/j.redox.2024.103062. https://pubmed.ncbi.nlm.nih.gov/38320454/

2. Aggeletopoulou, Ioanna, Thomopoulos, Konstantinos, Mouzaki, Athanasia, Triantos, Christos. 2022. Vitamin D-VDR Novel Anti-Inflammatory Molecules-New Insights into Their Effects on Liver Diseases. In International journal of molecular sciences, 23, . doi:10.3390/ijms23158465. https://pubmed.ncbi.nlm.nih.gov/35955597/

3. Shang, Mei, Sun, Jun. . Vitamin D/VDR, Probiotics, and Gastrointestinal Diseases. In Current medicinal chemistry, 24, 876-887. doi:10.2174/0929867323666161202150008. https://pubmed.ncbi.nlm.nih.gov/27915988/

4. Bakke, Danika, Sun, Jun. . Ancient Nuclear Receptor VDR With New Functions: Microbiome and Inflammation. In Inflammatory bowel diseases, 24, 1149-1154. doi:10.1093/ibd/izy092. https://pubmed.ncbi.nlm.nih.gov/29718408/

5. Glenn, Denis J, Cardema, Michelle C, Gardner, David G. 2015. Amplification of lipotoxic cardiomyopathy in the VDR gene knockout mouse. In The Journal of steroid biochemistry and molecular biology, 164, 292-298. doi:10.1016/j.jsbmb.2015.09.034. https://pubmed.ncbi.nlm.nih.gov/26429397/

Quality Control Standard
Sperm Test

Pre-cryopreservation: Measurement of sperm concentration, determination of sperm viability.

Post-cryopreservation: A vial of cryopreserved sperms is selected for in-vitro fertilization from each batch.

Environmental Standards:SPF
Available Region:Global
Source:Cyagen
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