Study of histology in accellular dermal matrix after being transplanted in vivo over time
10.3969/j.issn.1006-5725.2016.11.007
- VernacularTitle:脱细胞真皮基质移植后组织学转归的实验研究
- Author:
Ting LIAO
;
Rui ZOU
;
Jing YAN
;
Shan TANG
;
Zhengguo PIAO
- Publication Type:Journal Article
- Keywords:
Acellular dermal matrix;
Tissue remodeling;
Collagen;
Macrophage polarization
- From:
The Journal of Practical Medicine
2016;32(11):1749-1752
- CountryChina
- Language:Chinese
-
Abstract:
Objective To demonstrate the histology in acellular dermal matrix(ADM)after being transplanted in vivo over time. Methods Forty male SD rats were recruited for the experiment. Subcutaneous implantation of an 1 cm × 1 cm ADM was given in the left sides on the back of the rat for the experimental group, while only dissection and suturing were performed in right side of the back for the control group. All the animals will be sacrificed at appointed time after operation, Five ADM samples were harvested in each time point. The content and proportion of collagen type were examined with HE staining, Picrosirius staining, Masson′s trichrome staining, and Immunohistochemical staining (targets: pan macrophage, M1 macrophage and M2 macrophage). Results All rats survived after operative without any complications. Significant differences of thickness were not observed at the end of 5 months; HE scores suggested that ADM increased in cell infiltration scores in 2 weeks before the plateau , vascularity also showed a similar trend; Collagen trichrome staining showed a substantial increase in density of collagen bundles with time. The comparison of the proportion of collagen among days showed significant differences (P < 0.05). Immunohistochemical staining of M1 and M2 showed that macrophages had distinct polarization profiles in materials. Furthermore, the comparison of M1 vs M2 response associated with different materials showed significant differences in all time points (P < 0.05). Conclusions The chemically cross-linked ADM could keep long time in the body; ADM significantly stimulated proinflammatory of M2 differentiation from M1 in constructive remodeling.
