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©The Author(s) 2022.
World J Gastroenterol. Dec 14, 2022; 28(46): 6537-6550
Published online Dec 14, 2022. doi: 10.3748/wjg.v28.i46.6537
Published online Dec 14, 2022. doi: 10.3748/wjg.v28.i46.6537
Figure 1 Immune cell infiltration during the process of carbon tetrachloride-induced liver injury and repair.
A-C: The levels of serum alanine transaminase, aspartate transaminase and total bilirubin in carbon tetrachloride (CCl4)-treated wild-type mice; D-H: Quantitative changes in the infiltration of various immune cells in the livers of CCl4-treated wild-type mice. The data represent the mean ± SD. aP < 0.05; bP < 0.01; cP < 0.001; dP < 0.0001. ctrl: Control; ns: Not significant; ALT: Alanine transaminase; AST: Aspartate transaminase; TBil: Total bilirubin.
Figure 2 Immune cell infiltration during the process of concanavalin A-induced liver injury and repair.
A-C: The levels of serum alanine transaminase, aspartate transaminase and total bilirubin in concanavalin A (ConA)-treated wild-type mice; D-H: Quantitative changes in the infiltration of various immune cells in the livers of ConA-treated wild-type mice. The data represent the mean ± SD. aP < 0.05; bP < 0.01; cP < 0.001; dP < 0.0001. ctrl: Control; ns: Not significant; ALT: Alanine transaminase; AST: Aspartate transaminase; TBil: Total bilirubin.
Figure 3 The expression of leukocyte cell-derived chemotaxin 2 was increased in acute liver injury models.
A: The relative expression of Lect2 mRNA in the liver tissues of carbon tetrachloride (CCl4)-treated wild-type mice; B The levels of serum leukocyte cell-derived chemotaxin 2 (LECT2) in CCl4-treated wild-type mice; C: The relative expression of Lect2 mRNA in the liver tissues of concanavalin A (ConA)-treated wild-type mice; D: The levels of serum LECT2 in ConA-treated wild-type mice. The data represent the mean ± SD. ctrl: Control; ns: Not significant; aP < 0.05; bP < 0.01; cP < 0.001; dP < 0.0001. ctrl: Control; ns: Not significant; LECT2: Leukocyte cell-derived chemotaxin 2.
Figure 4 Lect2-KO mice showed less severe liver injuries.
A and B: The levels of serum alanine transaminase (ALT) and aspartate transaminase (AST) in the wild-type and Lect2-KO mice, with or without carbon tetrachloride treatment; C and D: The levels of serum ALT and AST in the wild-type and Lect2-KO mice, with or without concanavalin A treatment. The data represent the mean ± SD. aP < 0.05; bP < 0.01. ns: Not significant; ALT: Alanine transaminase; AST: Aspartate transaminase.
Figure 5 The effect of leukocyte cell-derived chemotaxin 2 on immune cell infiltration in the carbon tetrachloride-induced acute liver injury model.
A-E: Quantitative changes in the infiltration of various immune cells in the livers of wild-type and Lect2-KO mice, with or without carbon tetrachloride (CCl4) treatment; F: Representative images of infiltrated immune cells in CCl4-treated wild-type and Lect2-KO mice, with or without CCl4 treatment. The data represent the mean ± SD. ns: Not significant; aP < 0.05; bP < 0.01; cP < 0.001; dP < 0.0001. Scale bar: 50 μm.
Figure 6 The effect of leukocyte cell-derived chemotaxin 2 on immune cell infiltration in the concanavalin A-induced acute liver injury model.
A-E: Quantitative changes in the infiltration of various immune cells in the livers of wild-type and Lect2-KO mice, with or without concanavalin A (ConA) treatment; F: Representative images of infiltrated immune cells in ConA-treated wild-type and Lect2-KO mice, with or without ConA treatment. The data represent the mean ± SD. aP < 0.05; bP < 0.01; cP < 0.001; dP < 0.0001. ns: Not significant; Scale bar: 50 μm.
Figure 7 Chemokine-related genes changed in Lect2-KO mice.
A: Kyoto Encyclopedia of Genes and Genomes (KEGG) analysis results for carbon tetrachloride (CCl4)-treated Lect2-KO and wild-type mice; B: KEGG analysis results for concanavalin A (ConA)-treated Lect2-KO and wild-type mice; C: Heatmap of the differentially expressed chemokine-related genes between the Lect2-KO and wild-type mice after CCl4 treatment; D: Heatmap of the differentially expressed chemokine-related genes between the Lect2-KO and wild-type mice after ConA treatment.
Figure 8 Leukocyte cell-derived chemotaxin 2 promoted THP-1 monocyte chemotaxis.
A: Chemotactic effects of Lect2 on THP-1 cells when treated with different doses; B: Comparison of chemotactic effects between Lect2 and MCP-1. The data represent the mean ± SD. aP < 0.05; bP < 0.01. ctrl: Control.
- Citation: Xie Y, Zhong KB, Hu Y, Xi YL, Guan SX, Xu M, Lin Y, Liu FY, Zhou WJ, Gao Y. Liver infiltration of multiple immune cells during the process of acute liver injury and repair. World J Gastroenterol 2022; 28(46): 6537-6550
- URL: https://www.wjgnet.com/1007-9327/full/v28/i46/6537.htm
- DOI: https://dx.doi.org/10.3748/wjg.v28.i46.6537