Inhibition of mitogen-induced changes in intracellular fluorescein fluorescence polarization of human peripheral blood lymphocytes by colchicine, vinblastine and cytochalasin B

被引:10
作者
Eisenthal, A
Marder, O
LifschitzMercer, B
Skornick, Y
Tirosh, R
Weinreb, A
Deutsch, M
机构
[1] BAR ILAN UNIV, DEPT PHYS, JEROME SCHOTTENSTEIN CELLSCAN CTR EARLY DETECT CA, RAMAT GAN, ISRAEL
[2] TEL AVIV UNIV, SACKLER SCH MED, SOURASKY MED CTR, INST PATHOL, IL-69978 TEL AVIV, ISRAEL
关键词
cytoskeleton; activation; lymphocytes; human; fluorescence;
D O I
10.1247/csf.21.159
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
We have previously reported that the exposure of human peripheral blood lymphocytes (PBL) to a variety of stimulants caused rapid changes in intracellular fluorescein fluorescence polarization (IFFP) in the activated cells. In the present study we further analyzed possible mechanisms responsible for the changes in IFFP in PBL exposed to phytohaemagglutinin (PHA) and anti-CD3 antibody. By employing several agents which are known to affect the polymerization of the cytoskeleton we showed that both cytochalasin B, which regulates the microfilaments structure, and vinblastine and colchicine, which affect the microtubules, completely abolished the changes induced in IFFP of human PBL by both PHA and anti-CD3. This effect was dose dependent and was noted at concentrations ranging from 10 to 100 mu M of cytochalasin B and 10 mu M of vinblastine and colchicine. The effect of these cytoskeleton modulators occurred within 20 minutes after the initiation of activation with PHA. Our results indicate that activation with PHA and anti-CD3 causes early changes in the microtubules and microfilaments components of the cytoskeleton. The possible application of IFFP measurement in analyzing early changes in the cytoskeleton following cell activation is discussed.
引用
收藏
页码:159 / 166
页数:8
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