Preliminary study on preparation of decellularized nerve grafts from GGTA1 gene-edited pigs and their immune rejection in xenotransplantation.
10.7507/1002-1892.202408052
- Author:
Yuli LIU
1
;
Jinjuan ZHAO
2
;
Xiangyu SONG
2
;
Zhibo JIA
2
;
Chaochao LI
2
;
Tieyuan ZHANG
2
;
Xiangling LI
2
;
Shi YAN
2
;
Ruichao HE
2
;
Jiang PENG
2
Author Information
1. Graduate School, Guizhou Medical University, Guiyang Guizhou, 550005, P. R. China.
2. Institute of Orthopedics, General Hospital of Chinese PLA, Beijing, 100853, P. R. China.
- Publication Type:Journal Article
- Keywords:
GGTA1 gene-edited pig;
decellularized matrix;
peripheral nerve;
repair;
xenotransplantation
- MeSH:
Animals;
Transplantation, Heterologous;
Galactosyltransferases/genetics*;
Sciatic Nerve/immunology*;
Swine;
Tissue Engineering/methods*;
Humans;
Graft Rejection/prevention & control*;
Gene Editing;
Mice;
Mice, Nude;
Heterografts/immunology*;
Animals, Genetically Modified;
Tissue Scaffolds;
Decellularized Extracellular Matrix
- From:
Chinese Journal of Reparative and Reconstructive Surgery
2025;39(2):224-229
- CountryChina
- Language:Chinese
-
Abstract:
OBJECTIVE:To prepare decellularized nerve grafts from alpha-1, 3-galactosyltransferase (GGTA1) gene-edited pigs and explore their biocompatibility for xenotransplantation.
METHODS:The sciatic nerves from wild-type pigs and GGTA1 gene-edited pigs were obtained and underwent decellularization. The alpha-galactosidase (α-gal) content in the sciatic nerves of GGTA1 gene-edited pigs was detected by using IB4 fluorescence staining and ELISA method to verify the knockout status of the GGTA1 gene, and using human sciatic nerve as a control. HE staining and scanning electron microscopy observation were used to observe the structure of the nerve samples. Immunofluorescence staining and DNA content determination were used to evaluate the degree of decellularization of the nerve samples. Fourteen nude mice were taken, and subcutaneous capsules were prepared on both sides of the spine. Decellularized nerve samples of wild-type pigs ( n=7) and GGTA1 gene-edited pigs ( n=7) were randomly implanted in the subcutaneous capsules. Blood was drawn at 1, 3, 5, and 7 days after implantation to detect neutrophil counting.
RESULTS:IB4 fluorescence staining and ELISA detection showed that GGTA1 gene was successfully knocked out in the nerves of GGTA1 gene-edited pigs. HE staining showed that the structure of the decellularized nerve from GGTA1 gene-edited pigs was well preserved; the nerve basement membrane tube structure was visible under scanning electron microscopy; no cell nuclei was observed, and the extracellular matrix components was retained in the nerve grafts by immunofluorescence staining; and the DNA content was significantly reduced when compared with the normal nerves ( P<0.05). In vivo experiments showed that the number of neutrophils in the two groups were similar at 1, 3, and 7 days after implantation, with no significant difference ( P>0.05); only at 5 days, the number of neutrophils was significantly lower in the GGTA1 gene-edited pigs than in the wild-type pigs ( P<0.05).
CONCLUSION:The decellularized nerve grafts from GGTA1 gene-edited pigs have well-preserved nerve structure, complete decellularization, retain the natural nerve basement membrane tube structure and components, and low immune response after xenotransplantation through in vitro experiments.
