Function of IL-33 in Wound Age Estimation of Skin Wounds in Mice.
10.12116/j.issn.1004-5619.2020.02.009
- Author:
Yi YAO
1
;
Jun Jie HUANG
1
;
Xin JIN
1
;
Jian Xin ZHAO
1
;
Chong Jian XIA
1
;
Yan TONG
1
;
Yuan GAO
1
;
Lin Sheng YU
1
;
Yan Yan FAN
1
Author Information
1. Department of Forensic Medicine, Wenzhou Medical University, Wenzhou 325035, Zhejiang Province, China.
- Publication Type:Journal Article
- Keywords:
forensic pathology;
interleukin-33;
wound healing;
skin;
wound age estimation;
mice
- MeSH:
Animals;
Interleukin-33;
Mice;
Myofibroblasts;
Skin;
Soft Tissue Injuries;
Wound Healing
- From:
Journal of Forensic Medicine
2020;36(2):192-198
- CountryChina
- Language:English
-
Abstract:
Objective To explore the application value of interleukin-33 （IL-33） in wound age estimation in forensic practice by observing the sequential changes of IL-33 after skin wound. Methods Skin wound models were generated on the back of mice with a round file of 5 mm in diameter. Skin samples of the same size were taken from the same parts of mice in control group and injury group 1 h, 3 h, 6 h, 12 h, 1 d, 3 d, 5 d, 7 d and 10 d after skin wound. Hematoxylin-eosin （HE） staining method was applied to observe the morphological changes in the recovering process after skin wound. Western blotting, immunohistochemistry staining and double immunofluorescence staining methods were applied to detect the expression changes of IL-33 in the skin wound samples. Results The results of Western blotting showed that the expression of IL-33 protein decreased slightly at 3 h after skin wound, increased gradually at 6 h after skin wound, and reached the peak value at 3 d, then decreased gradually. Immunohistochemistry staining results showed that faint positive expression of IL-33 was observed in epidermis, hair follicles, sebaceous glands and dermal resident cells of the control group skin. The positive cell rate of IL-33 increased at 3 h after skin wound and reached the peak value at 3 d, then decreased gradually. The results of double immunofluorescence staining showed that the majority of IL-33 positive cells from 1 d to 3 d after wound were macrophages, while the majority of IL-33 positive cells from 5 d to 7 d after wound were myofibroblasts. In addition, the results of HE staining showed that the wound healing process of the skin wound model was consistent with the pathological development law of inflammation. Conclusion IL-33 could become a reference index for wound age estimation of skin wound in forensic practice.
