CHINESE JOURNAL OF PARASITOLOGY AND PARASITIC DISEASES ›› 2019, Vol. 37 ›› Issue (3): 302-310.doi: 10.12140/j.issn.1000-7423.2019.03.011
• ORIGINAL ARTICLES • Previous Articles Next Articles
Qing ZHOU1(), Xiong-feng YANG1, Huan-huan HAN1, Li-jiao GUO1, Hui-jiao JIANG1, Xiao-yi WANG1, Lin-lin LI2, Zhen-yu LIAO2, Xue-ling CHEN2, Xiang-wei WU1,*(
)
Received:
2018-11-15
Online:
2019-06-30
Published:
2019-07-10
Contact:
Xiang-wei WU
E-mail:404915195@qq.com;wxwshz@126.com
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CLC Number:
Qing ZHOU, Xiong-feng YANG, Huan-huan HAN, Li-jiao GUO, Hui-jiao JIANG, Xiao-yi WANG, Lin-lin LI, Zhen-yu LIAO, Xue-ling CHEN, Xiang-wei WU. Correlation between angiogenesis and disease progression of hepatic Echinococcus multilocularis in C57BL/6 mice[J]. CHINESE JOURNAL OF PARASITOLOGY AND PARASITIC DISEASES, 2019, 37(3): 302-310.
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URL: https://www.jsczz.cn/EN/10.12140/j.issn.1000-7423.2019.03.011
Fig. 1
Dynamic distribution of blood vessels around the infected Em in the livers of mice A-D: E. multilocularis infected mouse livers; E-H: Normal mouse livers. A: Em tissue was small, peripheral blood vessels were not clear at 30 d after infection; B: Em tissue was slightly larger, in irregular shape at 60 d after infection; C: Em tissue continued to grow, blood vessels were more obvious at 90 d after infection; D: Em tissue largely grew, clearly surrounded by peripheral blood vessels at 120 d after infection; E-H: No obvious abnormalities in the hepatic vasculature in control mice after 30, 60, 90, 120 d
Fig. 2
Pathological changes of mouse livers after being infected with E. multilocularis(HE staining, × 100) A-D: E. multilocularis infected mouse livers; E-H: Normal mouse livers. A: Em tissure was surrounded by the filtration of inflammatory cells. The protoscoleces and calcification were visible inside Em at 30 d after infection; B: Em was seriously surrounded by the infiltration of inflammatory cells and some protoscoleces observed inside Em at 60 d after infection; C: Em tissue further grew in the liver, and necrosis was visible inside Em tissue at 90 d after infection; D: Serious necrosis and empty vesicles could be seen in Em tissue at 120 d after iinfection; E-H: Livers in control group for 30, 60, 90, 120 d, the liver tissue structure was basically normal
Fig. 3
Dynamic expression of VEGFA in E. multilocularis during its infection in mouse liver (EnVision, × 200) A-D: Em tissues in infected mouse liver; E-H: Liver tissues surrounding Em in infected mouse; I-L: Livers tissues in normal mouse. A: A small amount of VEGFA was stained in slight brownish yellow in the endothelial cells of Em at 30 d after infection; B: A medium amount of VEGFA stained in brownish yellow in the endothelial cells of Em at 60 d after infection; C: A large amount of VEGFA was stained in dark brown in the endothelial cells of Em at 90 d after infection; D: The VEGFA stained endothelial cells in the Em were significantly reduced, which were brownish brown at 120 d after infection; E-H: No obvious VEGFA staining was observed in the liver tissue surrounding tne infected Em tissues after being infected for 30, 60, 90 and 120 d, respectively; I-L: No obvious VEGFA staining was observed in the normal liver tissue of control mice after 30, 60, 90 and 120 d, respectively
Fig. 4
Dynamic expression of CD34-MVD in E. multilocularis during its infection in mouse livers(EnVision, × 200) A-D: Em tissues in infected mouse liver; E-H: Liver tissues surrounding Em in infected mouse; I-L: Livers tissues in normal mouse. A: A small amount of CD34-MVD was stained in slight brownish yellow in the endothelial cells of Em at 30 d after infection; B: A medium amount of CD34-MVD stained in brownish yellow in the endothelial cells of Em at 60 d after infection; C: A large amount of CD34-MVD stained in dark brown in the endothelial cells of Em at 90 d after infection; D: The CD34-MVD stained endothelial cells in Em were reduced, which were brownish brown at 120 d after infection; E-H: No obvious CD34-MVD staining was observed in the liver tissue surrounding in infected Em tissues after being infected for 30, 60, 90 and 120 d, respectively; I-L: No obvious CD34-MVD staining was observed in the normal liver tissue of control mice after 30, 60, 90 and 120 d, respectively
Fig. 5
Dynamic expression of CD31-MVD in E. multilocularis during its infection in mouse liver (EnVision, × 200) A-D: Em tissues in infected mouse liver; E-H: Liver tissues surrounding Em in infected mouse; I-L: Livers tissues in normal mouse. A: A small amount of CD31-MVD was stained in the endothelial cells of Em, with irregular shape at 30 d after infection; B: A medium amount of CD31-MVD stained in the endothelial cells of Em with fusiform or tubular shapes at 60 d after infection; C: A large amount of CD31-MVD stained in the endothelial cells of Em with regular shape at 90 d after infection; D: The CD31-MVD stained endothelial cells in Em were reduced with tubular shape at 120 d after infection; E-H: A large amount of CD31-MVD staining was observed in the liver nonepithelial cells surrounding infected Em tissues after being infected for 30, 60, 90 and 120 d, respectively; I-L: A large amount of CD31-MVD staining was observed in the normal liver nonepithelial cells after 30, 60, 90 and 120 d, respectively
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