Fluorescence polarization of 1,6‐diphenyl‐1,3,5‐hexatriene embedded in membranes of mouse leukemic L 1210 cells during the cell cycle
Fluorescence polarization of 1,6‐diphenyl‐1,3,5‐hexatriene embedded in membranes of mouse leukemic L 1210 cells during the cell cycle
复制标题
细胞周期期间嵌入小鼠白血病 L 1210 细胞膜中的 1,6-二苯基-1,3,5-己三烯的荧光偏振
DOI:
10.1016/0014-5793(78)80170-7
复制
发表时间:
1978
期刊:
影响因子:
3.5
通讯作者:
M. Monsigny
中科院分区:
文献类型:
--
作者:
A. Obrénovitch;C. Sené;M. Negre;M. Monsigny
Amongst the numerous events which occur during a cell cycle, several are localized at the level of cell surface membrane. By labelling normal and transformed cells with fluorescent lectins, changes occurring during the cell cycle have been demonstrated [1-3]. With normal cells, the binding of lectins increased during mitosis and with transformed cells it increased during interphase. Furthermore, intramembranous particles were aggregated during several phases of the cell cycle but not during the mitotic phase [4]. More recently, it was suggested that the fluidity of normal and transformed mammalian flbroblasts in culture decreased when the cell density increased [5, 6] and that the fluidity of various mammalian cells increased [7] when cells were stimulated for growth. All these results suggest that the cell membrane undergoes a dynamic change during different phases of cell cycle. In the present report, murine leukemic cells L 1210 were synchronized with colcemid and the expected changes were checked by fluorescence polarization measurements of 1, 6-diphenyl-l, 3, 5-hexatriene [8] embedded in lipid bilayer. These results are discussed on the basis of fluorescence decay studies of DPH incorporated in unsynchronized L 1210 cells [21].