Destruction of erythroleukaemic cells by photoactivation of endogenous porphyrins.

Selective destruction of Friend erythroleukaemic cells (FELC) was potentiated by stimulation of endogenous porphyrin synthesis followed by light sensitization. Endogenous porphyrin biosynthesis in FELC was induced by supplementation of 5-amino levulinic acid (5-ALA) at a concentration of 5 X 10(-4) M. The main accumulated product, after 4 days culture, was uroporphyrin, while after 8 days culture the cells were loaded with protoporphyrin, up to 1.5 micrograms 10(-7) cells. Photoirradiation of the cells for 2 min, accumulating endogenous porphyrins, induced cardinal deformations and cell disintegration in greater than 95% of the cells, as examined by scanning electron microscopy (SEM). The photodynamic destruction effects were dependent on cultivation time with 5-ALA. Flow cytometry analysis showed an immediate expansion of cell volume subsequent to irradiation, presumably a consequence of water influx. Transmission electron microscopy (TEM) of photosensitized cells after different time intervals of culture in 5-ALA medium, revealed initial damage to mitochondria and water influx into the nuclear envelope, after 2 days. After 3-4 days in culture the water influx phenomenon was pronounced, chromatin condensation took place and slight rupture of the outer membrane was detected. Cells photosensitized after 5-6 days of culture were completely disintegrated leaving a nuclear remnant and an enormously swollen nuclear envelope. The culture time dependence of the process, showed an interrelationship between the photodynamic effect and porphyrin accumulation sites in cellular compartments. The study presents a specific method for erythroleukaemic cell inactivation.

[1]  D. Kessel,et al.  Chemical, biologic and biophysical studies on 'hematoporphyrin derivative'. , 1985, Advances in experimental medicine and biology.

[2]  J. Moan,et al.  Tumor-localizing and photosensitizing properties of the main components of hematoporphyrin derivative. , 1984, Cancer research.

[3]  M C Berenbaum,et al.  In vivo biological activity of the components of haematoporphyrin derivative. , 1982, British Journal of Cancer.

[4]  D. Kessel,et al.  Localization and photosensitization of murine tumors in vivo and in vitro by a chlorin-porphyrin ester. , 1986, Cancer research.

[5]  P. Marks,et al.  Erythroleukemic differentiation. , 1978, Annual review of biochemistry.

[6]  T. Dubbelman,et al.  PHOTODYNAMIC GENERATION OF HYDROXYL RADICALS BY HEMATOPORPHYRIN DERIVATIVE AND LIGHT , 1986, Photochemistry and photobiology.

[7]  C. Salet Hematoporphyrin and hematoporphyrin-derivative photosensitization of mitochondria. , 1986, Biochimie.

[8]  R. Zucker,et al.  Cell volume decrease during Friend leukemia cell differentiation. , 1979, The journal of histochemistry and cytochemistry : official journal of the Histochemistry Society.

[9]  J. Moan,et al.  PORPHYRIN PHOTOSENSITIZATION OF PROTEINS IN CELL MEMBRANES AS STUDIED BY SPIN‐LABELLING AND BY QUANTIFICATION OF DTNB‐REACTIVE SH‐GROUPS , 1986, Photochemistry and photobiology.

[10]  D. Kessel,et al.  Tumor-localizing components of the porphyrin preparation hematoporphyrin derivative. , 1983, Cancer research.

[11]  Z. Malik,et al.  5-Aminolevulinic acid stimulation of porphyrin and hemoglobin synthesis by uninduced Friend erythroleukemic cells. , 1979, Cell differentiation.

[12]  J. B. Rattner,et al.  The higher-order structure of chromatin: evidence for a helical ribbon arrangement , 1984, The Journal of cell biology.

[13]  H. Breitbart,et al.  THE EFFECTS OF PHOTOACTIVATED PROTOPORPHYRIN ON RETICULOCYTE MEMBRANES, INTRACELLULAR ACTIVITIES and HEMOGLOBIN PRECIPITATION , 1982, Photochemistry and photobiology.

[14]  E. Land Porphyrin phototherapy of human cancer. , 1984, International journal of radiation biology and related studies in physics, chemistry, and medicine.

[15]  S. Sassa,et al.  Sequential induction of heme pathway enzymes during erythroid differentiation of mouse Friend leukemia virus-infected cells , 1976, The Journal of experimental medicine.

[16]  H. Gamliel Optimum fixation conditions may allow air drying of soft biological specimens with minimum cell shrinkage and maximum preservation of surface features. , 1985, Scanning electron microscopy.

[17]  P. Ponka,et al.  Control of heme synthesis during Friend cell differentiation: Role of iron and transferrin , 1986, Journal of cellular physiology.

[18]  J C Kennedy,et al.  NON‐INVASIVE TECHNIQUE FOR OBTAINING FLUORESCENCE EXCITATION AND EMISSION SPECTRA IN VIVO , 1986, Photochemistry and photobiology.

[19]  H. Verweij,et al.  Photodynamic membrane damage. , 1983, Advances in experimental medicine and biology.

[20]  L. Rasetti,et al.  Porphyrin metabolism in human neoplastic tissues. , 1966, Panminerva medica.

[21]  D. Kessel SITES OF PHOTOSENSITIZATION BY DERIVATIVES OF HEMATOPORPHYRIN , 1986, Photochemistry and photobiology.