Affiliation:
1. Departments of Medicine1 and
2. Molecular Microbiology,2 Washington University School of Medicine, St. Louis, Missouri 63110
Abstract
ABSTRACT
Amebic liver abscess is characterized by extensive areas of dead hepatocytes that form cavities surrounded by a thin rim of inflammatory cells and few
Entamoeba histolytica
trophozoites.
E. histolytica
produces pore-forming proteins and proteinases, but how trophozoites actually kill host cells has been unclear. Here, we report that
E. histolytica
induces apoptosis in both inflammatory cells and hepatocytes in a severe combined immunodeficient (SCID) mouse model of amebic liver abscess. By studying infection in C57/BL6.lpr and C57/BL6.gld mice, we found that
E. histolytica
-induced apoptosis does not require the Fas/Fas ligand pathway of apoptosis, and by using mice with a targeted deletion of the tumor necrosis factor receptor I gene, we have shown that
E. histolytica
-induced apoptosis is not mediated by tumor necrosis factor alpha. Our data indicate that apoptosis plays a prominent role in the host cell death seen in amebic liver abscess in a mouse model of disease and suggest that
E. histolytica
induces cell death without using two common pathways for apoptosis.
Publisher
American Society for Microbiology
Subject
Infectious Diseases,Immunology,Microbiology,Parasitology
Cited by
99 articles.
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