Prolongation of functional life-span of neutrophils by recombinant verotoxin 2.
- Author:
Jiajia LIU
1
;
Tao HE
;
Yanzheng HE
;
Zhongjie ZHANG
;
Tohru AKAHOSHI
;
Hirobumi KONDO
;
Sen ZHONG
Author Information
- Publication Type:Journal Article
- MeSH: Apoptosis; drug effects; Cell Adhesion; Endothelium, Vascular; cytology; Humans; Neutrophils; drug effects; physiology; Recombinant Proteins; toxicity; Shiga Toxin 2; toxicity; Superoxides; metabolism
- From: Chinese Medical Journal 2002;115(6):900-903
- CountryChina
- Language:English
-
Abstract:
OBJECTIVEVerotoxin-producing Escherichia coli (VTEC) strains of serotype O157 : H7 have been implicated in a wide spectrum of diseases, including blood diarrhea, hemorrhagic colitis and hemolytic uremic syndrome (HUS). To further explore the pathological role of verotoxin (VT) in HUS and other VTEC associated diseases, we investigated the effects of recombinant verotoxin 2 (rVT2) on the biological activity of neutrophils.
METHODSThe technique of flow cytometry, a fluorescent probe 2,7-bis-(2-carboxyethyl)-5-(and-6)-carboxyfluorescein acetoxymethyl ester (BCECF/AM), and the assay of reduced cytochrome c to detect superoxide production were used in this study.
RESULTSgammaVT2 significantly inhibited spontaneous apoptosis in neutrophils. Neutrophils with prolonged survival due to gammaVT2 maintained various biological functions, such as the expression of adhesion molecules (shading CD62L and raising CD11b/CD18), adherence to human umbilical vein endothelial cells (HUVECs), and generation of superoxide (O(2)(-)).
CONCLUSIONProlongation of the functional life-span of neutrophils by gammaVT2 may accelerate inflammatory responses at sites of inflammation. This may play a crucial role in neutrophil-mediated tissue injury in HUS and other VTEC-associated diseases.
