Effect of intraperitoneal injection of anti-IL-33 antibody on hepatic fibrosis induced by CCl4 in mice
Haijun Zhu, Qiongqiong Yan, Wei Chen, Nang Jiang, Shaoyong Zhang, Limin Tian, Bo Sun
Abstract
Haijun Zhu, Qiongqiong Yan, Wei Chen, Nang Jiang, Shaoyong Zhang, Limin Tian, Bo Sun
Abstract
Objective To study the role of IL-33 in the pathogenesis of liver fibrosis. Methods Carbon tetrachloride(CCl4)-induced mouse liver fibrosis model was established in C57BL/6J mice Twenty C57BL/6J mice were randomly divided into control group, model group, antibody blocking group and homologous control group with 5 mice in each group..After intraperitoneal administration of interleukin(IL)-33 antibody, serum biochemistry, enzyme-linked immunosorbent assay(ELISA) and real-time quantitative polymerase chain reaction(qPCR) were used to detect liver fibrosis changes in related indicators. Results Compaired with the control group, the levels of IL-33[(18303.1±580.4)pg/mL vs.(4424.2±566.9)pg/mL, P<0.05], IL-4[(707.2±83.8)pg/mL vs.(50.2±2.1)pg/mL, P<0.05], and IL-13[(665.8±75.7)pg/mL vs.(37.8±7.8)pg/mL, P<0.05] in the liver tissue of the model group were significantly increased, while serum aspartate aminotransferase(AST)[(7503.4±614.2)IU/L vs.(44.2±5.7)IU/L, P<0.05] and alanine aminotransferase (ALT)[(6106.2±465.7)IU/L vs.(44.2±5.7)IU/L, P<0.05] levels were also elevated.The expression of matrix metalloproteinases(MMP)2 [(3.86±0.23)vs.(1.00±0.04), P<0.05] and MMP9 [(3.36±0.19)vs.(1.00±0.04), P<0.05] in the liver tissue of model group mice were significantly elevated and the collagen was significantly deposited[(2704.0±83.3)μg/mL vs.(1425.4±37.0)μg/mL, P<0.05]. After blocking IL-33 with antibodies, IL-4[(707.2±83.8)pg/mL vs.(344.6±51.6)pg/mL, P<0.05 and IL-13 [(665.8±75.7)pg/mL vs.(284.6±65.8)pg/mL, P<0.05] in liver homogenates of model group mice were significantly reduced, and the levels of AST[(7503.4±614.2)IU/L vs.(3883.2±317.0) IU/L, P<0.05] and ALT[(6106.2±465.7)IU/L vs.(3684.4±169.0)IU/L, P<0.05] in serum were significantly decreased compared with control group.The expression of MMP2[(3.86±0.23) vs.(1.94±0.17), P<0.05] and MMP9 [(3.36±0.19)vs.(2.20±0.13), P<0.05] were significantly reduced in the liver tissue of model group mice, and the deposition of collagen was also significantly reduced [(2704.0±83.3)μg/mL vs.(1894.2±174.1)μg/mL, P<0.05]. Conclusion IL-33 is closely related to the pathogenesis of liver fibrosis.Blocking IL-33 may become a new strategy to treat hepatic fibrosis. Key words: Liver fibrosis; Interleukin-33
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Objective To study the role of IL-33 in the pathogenesis of liver fibrosis. Methods Carbon tetrachloride(CCl4)-induced mouse liver fibrosis model was established in C57BL/6J mice Twenty C57BL/6J mice were randomly divided into control group, model group, antibody blocking group and homologous control group with 5 mice in each group..After intraperitoneal administration of interleukin(IL)-33 antibody, serum biochemistry, enzyme-linked immunosorbent assay(ELISA) and real-time quantitative polymerase chain reaction(qPCR) were used to detect liver fibrosis changes in related indicators. Results Compaired with the control group, the levels of IL-33[(18303.1±580.4)pg/mL vs.(4424.2±566.9)pg/mL, P<0.05], IL-4[(707.2±83.8)pg/mL vs.(50.2±2.1)pg/mL, P<0.05], and IL-13[(665.8±75.7)pg/mL vs.(37.8±7.8)pg/mL, P<0.05] in the liver tissue of the model group were significantly increased, while serum aspartate aminotransferase(AST)[(7503.4±614.2)IU/L vs.(44.2±5.7)IU/L, P<0.05] and alanine aminotransferase (ALT)[(6106.2±465.7)IU/L vs.(44.2±5.7)IU/L, P<0.05] levels were also elevated.The expression of matrix metalloproteinases(MMP)2 [(3.86±0.23)vs.(1.00±0.04), P<0.05] and MMP9 [(3.36±0.19)vs.(1.00±0.04), P<0.05] in the liver tissue of model group mice were significantly elevated and the collagen was significantly deposited[(2704.0±83.3)μg/mL vs.(1425.4±37.0)μg/mL, P<0.05]. After blocking IL-33 with antibodies, IL-4[(707.2±83.8)pg/mL vs.(344.6±51.6)pg/mL, P<0.05 and IL-13 [(665.8±75.7)pg/mL vs.(284.6±65.8)pg/mL, P<0.05] in liver homogenates of model group mice were significantly reduced, and the levels of AST[(7503.4±614.2)IU/L vs.(3883.2±317.0) IU/L, P<0.05] and ALT[(6106.2±465.7)IU/L vs.(3684.4±169.0)IU/L, P<0.05] in serum were significantly decreased compared with control group.The expression of MMP2[(3.86±0.23) vs.(1.94±0.17), P<0.05] and MMP9 [(3.36±0.19)vs.(2.20±0.13), P<0.05] were significantly reduced in the liver tissue of model group mice, and the deposition of collagen was also significantly reduced [(2704.0±83.3)μg/mL vs.(1894.2±174.1)μg/mL, P<0.05]. Conclusion IL-33 is closely related to the pathogenesis of liver fibrosis.Blocking IL-33 may become a new strategy to treat hepatic fibrosis. Key words: Liver fibrosis; Interleukin-33
Key concepts: Carbon tetrachloride, CCL4, Internal medicine, Endocrinology, Intraperitoneal injection, Medicine, Pathogenesis, Fibrosis