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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 />

121.<br />

OVEREXPRESSION OF P-GLYCOPROTEIN IN L1210/VCR CELLS IS<br />

ASSOCIATED WITH CHANGES IN SEVEraL ENDOPLASMIC RETICULUM<br />

PROTEINS<br />

Mário Šereš, Eva Poláková, Oľga Križanová, Zdena Sulová and Albert Breier<br />

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

Multidrug resistant cells R, which express membrane drug efflux transporter – P-glycoprotein<br />

(P-gp, a member of ABC transporter family), was found to be also less sensitive to thapsigargin,<br />

inhibitor of sarco(endo)plasmic reticulum calcium pump (SERCA), in contrast<br />

to parental drug-sensitive cells L1210 (S). R cells was obtained from S cells by selection<br />

with vincristine (VCR). We have studied differences among S and R cells in expression<br />

of endoplasmic reticulum proteins involved in the regulation of calcium homeostasis<br />

and calcium-dependent processes. Amounts of mRNA encoding RyR and IP 3<br />

-receptor<br />

channels were found to be at similar in S and R cells. However, mRNAs encoding IP 3<br />

R1<br />

or 2 were decreased in resistant cells cultivated in the presence of VCR, while mRNA<br />

encoding RyR remained unchanged. The amount of mRNA encoding SERCA2 was lower<br />

in R cells as in S cells. This decrease was more pronounced when R cells were cultivated<br />

in the presence of VCR. Calnexin was believed to be active in P-gp maturation, but surprisingly,<br />

calnexin was found to be less expressed at the protein level in R as in S cells.<br />

We have also studied thapsigargin effect on expression of some endoplasmic reticulum<br />

proteins and P-glycoprotein. P-gp expression was decreased in presence of thapsigargin.<br />

Thus, S and R cells differ in the expression of endoplasmic reticulum proteins involved<br />

in the control of intracellular calcium homeostasis or calcium-dependent processes.<br />

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

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

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

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