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...

Full description

Saved in:
Bibliographic Details
Published inThe Journal of infectious diseases Vol. 152; no. 3; pp. 542 - 549
Main Authors Ravdin, Jonathan I., Murphy, Cheryl F., Guerrant, Richard L., Long-Krug, Sharon A.
Format Journal Article
LanguageEnglish
Published Chicago, IL The University of Chicago Press 01.09.1985
University of Chicago Press
Subjects
Online AccessGet full text

Cover

Loading…
More Information
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.
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