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Trans-sialidase from Trypanosoma cruzi induces apoptosis in cells from the immune system in vivo.
- Source :
-
The Journal of infectious diseases [J Infect Dis] 1999 Oct; Vol. 180 (4), pp. 1398-402. - Publication Year :
- 1999
-
Abstract
- Trypanosoma cruzi, the etiologic agent of Chagas' disease, expresses trans-sialidase, an enzyme able to direct transfer of sialyl residues among macromolecules. The enzyme is shed and can be detected in blood during the acute phase of the disease. Several alterations of the immune response and apoptosis of cellular components of the immune system are observed early in the infection. The possible involvement of bloodstream trans-sialidase on these events was analyzed here. The enzyme induced apoptosis in cells of the immune system in the spleen, thymus, and peripheral ganglia. Both natural and recombinant trans-sialidases induced apoptosis to a similar extent. No effect was detected when enzymatically inactive recombinant molecules were used. In dose-response assays, apoptosis was observed even when an amount of trans-sialidase was administered that was enzymatically undetectable in blood. These findings strongly suggest a role for sialic acid mobilization in T. cruzi-induced apoptosis of immune system cells.
- Subjects :
- Animals
Chlorocebus aethiops
Female
Ganglia immunology
Immune System cytology
Immune System drug effects
In Situ Nick-End Labeling
Lymphocytes cytology
Lymphocytes drug effects
Mice
Mice, Inbred BALB C
Pregnancy
Recombinant Proteins pharmacology
Spleen immunology
T-Lymphocytes cytology
T-Lymphocytes drug effects
T-Lymphocytes physiology
Trypanosoma cruzi enzymology
Trypanosoma cruzi immunology
Vero Cells
Antigens, Protozoan pharmacology
Apoptosis
Glycoproteins pharmacology
Immune System physiology
Lymphocytes physiology
Neuraminidase pharmacology
Subjects
Details
- Language :
- English
- ISSN :
- 0022-1899
- Volume :
- 180
- Issue :
- 4
- Database :
- MEDLINE
- Journal :
- The Journal of infectious diseases
- Publication Type :
- Academic Journal
- Accession number :
- 10479182
- Full Text :
- https://doi.org/10.1086/315001