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

J Photochem Photobiol B. 1997 May;39(1):49-55. doi: 10.1016/s1011-1344(96)07471-4.

Abstract

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 M1 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.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Erythrocytes / metabolism
  • Kinetics
  • Leukemia, Myeloid / metabolism*
  • Macrophages, Peritoneal / cytology
  • Mice
  • Mice, Inbred BALB C
  • Microscopy, Fluorescence
  • Phenotype
  • Photosensitizing Agents / metabolism*
  • Pyrimidinones / metabolism*
  • Spectrometry, Fluorescence
  • Tumor Cells, Cultured

Substances

  • Photosensitizing Agents
  • Pyrimidinones
  • merocyanine dye