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XXII. BIOCHEMICKÝ ZJAZD - Jesseniova lekárska fakulta

XXII. BIOCHEMICKÝ ZJAZD - Jesseniova lekárska fakulta

XXII. BIOCHEMICKÝ ZJAZD - Jesseniova lekárska fakulta

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Posters<br />

46.<br />

DifferENCES IN INTEraCTION of LECTINS SPECIfICaLLY rECOGNIZING<br />

SIaLIC aCID rESIDUES WITH SUrfaCE of P-GP NEGaTIve or POSITIve<br />

L1210 CELLS<br />

Tatiana Kurucová, Helena Kavcová, Kristína Rogozanová, Lucia Messingerova,<br />

Danica Mislovičová 1 , Albert Breier and Zdena Sulová<br />

Institute of Molecular Physiology and Genetics SAS, Bratislava, Slovakia<br />

1<br />

Institute of Chemistry SAS, Bratislava, Slovakia<br />

Multidrug resistance (MDR) of mouse leukemic cell line L1210/VCR (R) obtained by<br />

adaptation of L1210 cells (S) to vincristine (VCR) is accompanied by overexpression of<br />

P-glycoprotein (P-gp). Selection with VCR that confers overexpression of P-gp is also inducing<br />

various kinds of metabolic alteration. We described recently several differences<br />

in cell surface saccharides between R and S cells.<br />

Aim of this study was to resolve in exist differences in interaction of Triticum vulgaris<br />

lectin (WGA), Maackia amurensis lectin (MAA), Sambucus nigra lectin (SNA) with cell<br />

surface of S, R cells and L1210 cells that express P-gp due to transfection of cells with<br />

plasmid containing human gene encoding this protein (T cells). While MAA was found to<br />

be nontoxic for S, R and T cells and SNA is exerting small cell damage effect, WGA induced<br />

concentration depended cytotoxic effect. Agglutination of cells by this lectin is more massive<br />

to cells expressed P-gp. WGA lectin interact more potently with P-gp positive cells<br />

R and T as with P-gp negative S cells. Spectrum of cell membrane glycoprotein targets<br />

of lectins were assessed by lectin blot methods. Our data indicated that application of<br />

lectins enable to study the differences cell surface saccharides.<br />

Acknowledgements: This work was supported by: APVV-0084-07, VVCE-0064-07, VEGA-<br />

2/0123/10, VEGA-2/0155/09.<br />

<strong>XXII</strong>. Biochemistry Congress, Martin<br />

165

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