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Archives of Medical Research 2008-Oct

Lectin-induced aggregates of blood cells from patients with acute coronary syndromes.

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Odkaz sa uloží do schránky
Irina V Gorudko
Inna V Buko
Sergey N Cherenkevich
Leonid Z Polonetsky
Alexander V Timoshenko

Kľúčové slová

Abstrakt

BACKGROUND

Cell surface glycoligands and circulating glycoproteins are believed to contribute to the pathogenesis of acute coronary syndromes (ACS) through cell aggregation/adhesion mechanisms. To characterize the glycobiological status of blood cells from patients with ACS, we used an advanced lectin-mediated aggregation technique allowing for detection of not only conventional lectin-induced cell aggregates but also their fraction resistant to haptenic/inhibitory sugars.

METHODS

Peripheral blood samples were obtained from 24 patients with acute myocardial infarction or unstable angina and 18 healthy control subjects. Two plant lectins, Viscum album agglutinin (VAA) and wheat germ agglutinin (WGA), were tested as cell aggregation stimuli binding to cell membrane beta-galactosides and N-acetyl-D-glucosamine acid residues, respectively.

RESULTS

Two major types of differences were found between the clinical group and control: (1) VAA-induced aggregation of lymphocytes and platelets was decreased in ACS patients in comparison with healthy donors and (2) the stability of the lectin-induced cell aggregates was found to be an independent aggregation index that revealed opposite trends in the resistance of WGA-induced aggregates of platelets and neutrophils from ACS patients to haptenic sugars in comparison with respective controls. Thus, in the ACS group the stability of WGA-induced aggregates of platelets was impaired, whereas WGA-induced aggregates of neutrophils were more stable and their formation was accompanied by increased generation of H(2)O(2).

CONCLUSIONS

We conclude that (a) glycobiological status of blood cells undergoes a complex remodeling in association with ACS and (b) detection of lectin-induced stable aggregates can serve as a sensitive method for determination of cellular dysfunctions in ACS.

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