-
Categories
-
Pharmaceutical Intermediates
-
Active Pharmaceutical Ingredients
-
Food Additives
- Industrial Coatings
- Agrochemicals
- Dyes and Pigments
- Surfactant
- Flavors and Fragrances
- Chemical Reagents
- Catalyst and Auxiliary
- Natural Products
- Inorganic Chemistry
-
Organic Chemistry
-
Biochemical Engineering
- Analytical Chemistry
-
Cosmetic Ingredient
- Water Treatment Chemical
-
Pharmaceutical Intermediates
Promotion
ECHEMI Mall
Wholesale
Weekly Price
Exhibition
News
-
Trade Service
Successful construction of a pig model of human metabolic inflammation |
The liver and fat of a humanized mini-pig model of metabolic diseases show similar molecular characteristics of triggering metabolic inflammation as humans.
Image courtesy of the Chinese Academy of Agricultural Sciences
Image courtesy of the Chinese Academy of Agricultural Sciences
Recently, the animal genetic engineering and germplasm innovation technology innovation team of Beijing Institute of Animal Husbandry and Veterinary Medicine, Chinese Academy of Agricultural Sciences successfully constructed a pig model of human metabolic inflammation, providing important experimental materials for human metabolic inflammation translational medical research
.
Related research results were published in " Frontiers in Immunology " ( Frontiers in Immunology )
.
Frontiers in Immunology
According to researcher Yang Shulin of the institute, chronic, low-grade inflammation caused by overnutrition is the common pathogenesis of metabolic diseases such as obesity-related type 2 diabetes, non-alcoholic fatty liver disease, and atherosclerosis
.
Due to the huge immunological differences between rodents and humans, the efficiency of the conversion and application of related therapeutic drugs from trials to clinics is limited
.
The research team used multi-gene targeted integration technology to transfer three human metabolic disease susceptibility genes (GIPRdn, hIAPP and PNPLA3I148M) into the pig genome
.
The tissue-specific promoter regulates the expression of GIPRdn and hIAPP in pancreatic β-cells, and regulates the expression of human PNPLA3I148M in the liver.
This pig model exhibits pathological features such as impaired glucose tolerance, fatty pancreas, fat, and chronic liver inflammation
Through homology comparison of the protein sequences of 30 genes that play a key role in the process of inflammation, it is found that the similarity of 24 genes between pigs and humans is higher than that between rodents and humans.
The results show that the pig model fat and liver metabolic inflammation trigger and cascade molecular characteristics are highly similar to humans, and it is suitable as an experimental material for clinical translational medicine research
Related paper information: https://doi.
https://doi.
org/10.
3389/fimmu.
2021.
690069