Toll-like Receptor Agonist CBLB502 Protects Against Radiation-induced Intestinal Injury in Mice

被引:0
作者
Wang, Qiong [1 ,2 ]
Duan, Junzhao [2 ]
Hong, Jian [2 ,3 ]
Ding, Kexin [1 ]
Tai, Fumin [2 ]
Zhu, Jie [2 ]
Fu, Hanjiang [2 ]
Zheng, Xiaofei [2 ]
Ge, Changhui [1 ,2 ]
机构
[1] Anhui Med Univ, Sch Basic Med Sci, Hefei, Peoples R China
[2] Beijing Inst Radiat Med, Dept Expt Hematol & Biochem, Beijing Key Lab Radiobiol, 27 Taiping Rd, Beijing 100850, Peoples R China
[3] Peoples Liberat Army Gen Hosp, Med Ctr 8, Beijing, Peoples R China
来源
IN VIVO | 2024年 / 38卷 / 04期
关键词
Ionizing radiation; CBLB502; TLR5; agonist; intestinal; injury; toll -like receptor; INDUCED APOPTOSIS; DAMAGE; GENE; BST2;
D O I
10.21873/invivo.13613
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
Background/Aim: The small intestine is one of the organs most vulnerable to ionizing radiation (IR) damage. However, methods to protect against IR-induced intestinal injury are limited. CBLB502, a Toll-like receptor 5 (TLR5) agonist from Salmonella flagellin, exerts radioprotective effects on various tissues and organs. However, the molecular mechanisms by which CBLB502 protects against IR-induced intestinal injury remain unclear. Thus, this study aimed to elucidate the mechanisms underlying IR-induced intestinal injury and the protective effects of CBLB502 against this condition in mice. Materials and methods: Mice were administered 0.2 mg/kg CBLB502 before IR at different doses for different time points, and then the survival rate, body weight, hemogram, and histopathology of the mice were analyzed. Results: CBLB502 reduced IR-induced intestinal injury. RNA-seq analysis revealed that different doses and durations of IR induced different regulatory patterns. CBLB502 protected against intestinal injury mainly after IR by reversing the expression of IR-induced genes and regulating immune processes and metabolic pathways. Conclusion: This study preliminarily describes the regulatory mechanism of IR-induced intestinal injury and the potential molecular protective mechanism of CBLB502, providing a basis for identifying the functional genes and molecular mechanisms that mediate protection against IR-induced injury.
引用
收藏
页码:1636 / 1648
页数:13
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