Effect of Antagonists of Calcium and Phospholipase A on the Cytopathogenicity of Entamoeba histolytica
The in vitro mechanisms by which Entamoeba histolytica trophozoites lyse target Chinese hamster ovary(CHO) cells were examined. Calcium chelators ethylenediaminetetraacetate and ethyleneglycol bis (β-aminoethyl ether)-N,N′-tetraacetate (10mM) inhibited amebic cytolysis of target CHO cells (P < .0...
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Published in | The Journal of infectious diseases Vol. 152; no. 3; pp. 542 - 549 |
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Main Authors | , , , |
Format | Journal Article |
Language | English |
Published |
Chicago, IL
The University of Chicago Press
01.09.1985
University of Chicago Press |
Subjects | |
Online Access | Get full text |
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Summary: | The in vitro mechanisms by which Entamoeba histolytica trophozoites lyse target Chinese hamster ovary(CHO) cells were examined. Calcium chelators ethylenediaminetetraacetate and ethyleneglycol bis (β-aminoethyl ether)-N,N′-tetraacetate (10mM) inhibited amebic cytolysis of target CHO cells (P < .01). A putative antagonist of intracellular calcium flux, 8-(N,N-diethylamino)octyl-3,4,5-trimethoxybenzoate(TMB-8; ⩾250µM, inhibited amebic adherence and cytolysis (P <.001). Quinacrine, Rosenthal's inhibitor (dimethyl-dl-2,3-distearoyloxypropyl-2′-hydroxyethyl ammonium acetate), phosphatidylcholine, and hydrocortisone (⩾10− M), all pharmacological antagonists of eukaryotic phospholipase A enzymes, inhibited amebic killing of target CHO cells (P <.001). At 37 C quinacrine and hydrocortisone reduced amebic adherence to CHO cells, whereas Rosenthal's inhibitor and phosphatidylcholine did not. Phosphatidylcholine and TMB-8 demonstrated a synergistic inhibitory effect on amebic killing of target CHO cells(P < .001). These studies indicate that extracellular calcium ions, amebic intracellular calcium flux, and amebic phospholipase A activity are required for cytolysis of target cells by E. histolytica. |
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Bibliography: | This study was presented in part at the 22nd Interscience Conference on Antimicrobial Agents and Chemotherapy, held 3–6 October 1982, in Miami, Florida, and the meeting of the Southern Section of the American Federation for Clinical Research, held 27 January 1983, in New Orleans, Louisiana. istex:B4268D9EA5A20583BF6B66BF689E1872CC1EE013 ark:/67375/HXZ-GMF5V3G9-R ObjectType-Article-2 SourceType-Scholarly Journals-1 ObjectType-Feature-1 content type line 23 ObjectType-Article-1 ObjectType-Feature-2 |
ISSN: | 0022-1899 1537-6613 |
DOI: | 10.1093/infdis/152.3.542 |