A study of the binding of merocyanine 540 to myeloid leukemia M1 cells using an intensified charge-coupled device for fluorescence imaging microscopy

被引:11
作者
Chen, JY
Mak, NK
Leung, WN
Chen, SC
Leung, KN
Cheung, NH
机构
[1] HONG KONG BAPTIST UNIV,DEPT PHYS,HONG KONG,HONG KONG
[2] FUDAN UNIV,DEPT PHYS,SHANGHAI 200433,PEOPLES R CHINA
[3] HONG KONG BAPTIST UNIV,DEPT BIOL,HONG KONG,HONG KONG
[4] CHINESE UNIV HONG KONG,DEPT BIOCHEM,SHATIN,HONG KONG
关键词
fluorescence imaging microscopy; myeloid leukemia; merocyanine;
D O I
10.1016/S1011-1344(96)07471-4
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The binding of merocyanine 540 (MC540) to murine myeloid leukemia (M1) cells and normal erythrocytes was measured by fluorescence digital imaging microscopy using an intensified charge-coupled device. It was found that, on average, about three times more MC540 were bound to a unit membrane area of M1 cells than erythrocytes, a result consistent with previous studies. However, it was shown for the first time that MC540 binding varied significantly from one MI cell to the next, and about 15% of the sensitized M1 cells were as MC540-negative as normal erythrocytes. Using the leukemic inhibitory factor as a differentiation inducer, M1 cells were induced to differentiate into mature macrophage-like cells in vitro. Such treatment lowered the average MC540 binding by about one-third but did not affect the cell-to-cell variation significantly. (C) 1997 Elsevier Science S.A.
引用
收藏
页码:49 / 55
页数:7
相关论文
共 40 条
[1]   TIME-RESOLVED FLUORESCENCE SPECTROSCOPY AND INTRACELLULAR IMAGING OF DISULFONATED ALUMINUM PHTHALOCYANINE [J].
AMBROZ, M ;
MACROBERT, AJ ;
MORGAN, J ;
RUMBLES, G ;
FOLEY, MSC ;
PHILIPS, D .
JOURNAL OF PHOTOCHEMISTRY AND PHOTOBIOLOGY B-BIOLOGY, 1994, 22 (02) :105-117
[2]   SELECTIVE STAINING OF IMMATURE HEMATOPOIETIC-CELLS WITH MEROCYANINE-540 IN FLOW-CYTOMETRY [J].
BELLOC, F ;
LACOMBE, F ;
BERNARD, P ;
DACHARY, D ;
BOISSEAU, MR .
CYTOMETRY, 1988, 9 (01) :19-24
[3]   GRANULOCYTIC COLONY-STIMULATING FACTOR (G-CSF) DOES NOT INDUCE DIFFERENTIATION OF WEHI3B(D+) CELLS BUT IS REQUIRED FOR THE SURVIVAL OF THE MATURE PROGENY [J].
BOHMER, RM ;
BURGESS, AW .
INTERNATIONAL JOURNAL OF CANCER, 1988, 42 (01) :53-58
[4]  
CHEN JY, 1990, ACTA BIOL EXP SINICA, V23, P205
[5]   ALTERATIONS IN PLASMA-MEMBRANE LIPID ORGANIZATION DURING LYMPHOCYTE DIFFERENTIATION [J].
DELBUONO, BJ ;
WILLIAMSON, PL ;
SCHLEGEL, RA .
JOURNAL OF CELLULAR PHYSIOLOGY, 1986, 126 (03) :379-388
[6]   ABSORPTION AND EMISSION CHARACTERISTICS OF MEROCYANINE-540 IN MICROEMULSIONS [J].
DIXIT, NS ;
MACKAY, RA .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1983, 105 (09) :2928-2929
[7]   DECREASED EXPRESSION OF J11D-ANTIGEN DURING MONOCYTIC DIFFERENTIATION OF M1-MYELOID LEUKEMIC-CELLS [J].
FUNG, MC ;
MAK, NK ;
LEUNG, KN ;
HAPEL, AJ .
CELLULAR IMMUNOLOGY, 1992, 141 (01) :121-130
[8]  
GAFFNEY DK, 1990, CANCER RES, V50, P7765
[9]   THE ROLE OF SERUM AND SERUM COMPONENTS IN THE MEROCYANINE-540-SENSITIZED PHOTOINACTIVATION OF K562 LEUKEMIA-CELLS [J].
GAFFNEY, DK ;
SIEBER, F .
BIOCHIMICA ET BIOPHYSICA ACTA, 1992, 1117 (03) :321-325
[10]   CHOLESTEROL CONTENT BUT NOT PLASMA-MEMBRANE FLUIDITY INFLUENCES THE SUSCEPTIBILITY OF L1210 LEUKEMIA-CELLS TO MEROCYANINE 540-SENSITIZED IRRADIATION [J].
GAFFNEY, DK ;
FEIX, JB ;
SCHWARZ, HP ;
STRUVE, MF ;
SIEBER, F .
PHOTOCHEMISTRY AND PHOTOBIOLOGY, 1991, 54 (05) :717-723