LYSOSOMES, A KEY TARGET OF HYDROPHOBIC PHOTOSENSITIZERS PROPOSED FOR PHOTOCHEMOTHERAPEUTIC APPLICATIONS

被引:75
作者
GEZE, M
MORLIERE, P
MAZIERE, JC
SMITH, KM
SANTUS, R
机构
[1] MUSEUM NATL HIST NAT,PHYSICOCHIM ADAPTAT BIOL LAB,INSERM,U312,43 RUE CUVIER,F-75231 PARIS 05,FRANCE
[2] CHU HENRI MONDOR,INSERM,U312,DERMATOL LAB,F-94410 CRETEIL,FRANCE
[3] UNIV CALIF DAVIS,DEPT CHEM,DAVIS,CA 95616
基金
美国国家科学基金会;
关键词
CANCER PHOTODYNAMIC THERAPY; PORPHYRINS; CHLORINS; LOCALIZATION; LYSOSOMES; FIBROBLASTS; HT-29-18; CELLS; MICROSPECTROFLUOROMETRY; PHOTOSENSITIZATION; LIPOFUSCINS;
D O I
10.1016/1011-1344(93)80128-V
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
Despite their important biological activity, lysosomes have been generally neglected as important primary targets of photosensitizers, because they are not easily accessible for experiments. This paper reviews factors favoring the localization of photosensitizers in lysosomes and the various experimental approaches which have been used so far for the characterization of the lysosomal staining by various photosensitizing dyes, including porphyrins, chlorins and phenoxazines. The experimental difficulties observed in combining several in vitro techniques for the unambiguous demonstration of lysosomal targeting are examined. New data on tetraphenylporphine derivatives and a pyropheophorbide, as well as previous data on photofrin II, are presented to illustrate the advantages and possibilities of microspectrofluorometry in the study of photosensitizer localization in single living cells. Both spectral and topographic information available from areas smaller than 1 mum2 make it possible to characterize fairly specific sites of localization through the use of specific and vital fluorescent probes of lysosomes, such as Lucifer Yellow. It is also shown by microspectrofluorometry on single living cells that the chronology of the photosensitized reactions induced by specific or unspecific lysosomal photosensitizers can be easily followed. The photosensitized lipofuscin formation observed at the plasma membrane level with the lysosomotropic tetraphenylporphine supports the contention that it is very rare to find a truly specific lysosomal photosensitizer.
引用
收藏
页码:23 / 35
页数:13
相关论文
共 31 条
[1]  
ALISON AC, 1966, NATURE, V209, P874
[2]   PHOTOSENSITIZED DESTRUCTION OF HUMAN BLADDER-CARCINOMA CELLS TREATED WITH CHLORIN E6-CONJUGATED MICROSPHERES [J].
BACHOR, R ;
SHEA, CR ;
GILLIES, R ;
HASAN, T .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1991, 88 (04) :1580-1584
[3]   INTRACELLULAR-LOCALIZATION OF SULFONATED MESO-TETRAPHENYLPORPHINES IN A HUMAN CARCINOMA CELL-LINE [J].
BERG, K ;
WESTERN, A ;
BOMMER, JC ;
MOAN, J .
PHOTOCHEMISTRY AND PHOTOBIOLOGY, 1990, 52 (03) :481-487
[4]   LIGHT-INDUCED RELOCALIZATION OF SULFONATED MESO-TETRAPHENYLPORPHINES IN NHIK 3025 CELLS AND EFFECTS OF DOSE FRACTIONATION [J].
BERG, K ;
MADSLIEN, K ;
BOMMER, JC ;
OFTEBRO, R ;
WINKELMAN, JW ;
MOAN, J .
PHOTOCHEMISTRY AND PHOTOBIOLOGY, 1991, 53 (02) :203-210
[5]  
BERNS MW, 1982, CANCER RES, V42, P2325
[6]   LIPOPROTEIN METABOLISM IN THE MACROPHAGE - IMPLICATIONS FOR CHOLESTEROL DEPOSITION IN ATHEROSCLEROSIS [J].
BROWN, MS ;
GOLDSTEIN, JL .
ANNUAL REVIEW OF BIOCHEMISTRY, 1983, 52 :223-261
[7]   MODIFICATION OF EPSILON-AMINO GROUP OF LYSINES, CHOLESTEROL OXIDATION AND OXIDIZED LIPID APOPROTEIN CROSS-LINK FORMATION BY PORPHYRIN-PHOTOSENSITIZED OXIDATION OF HUMAN LOW-DENSITY LIPOPROTEINS [J].
CANDIDE, C ;
REYFTMANN, JP ;
SANTUS, R ;
MAZIERE, JC ;
MORLIERE, P ;
GOLDSTEIN, S .
PHOTOCHEMISTRY AND PHOTOBIOLOGY, 1988, 48 (02) :137-146
[8]  
CARRANO CJ, 1978, CHEM-BIOL INTERACT, V21, P233, DOI 10.1016/0009-2797(78)90022-4
[9]   A NEW METHOD FOR STUDYING EPIDERMALIZATION INVITRO [J].
COULOMB, B ;
SAIAG, P ;
BELL, E ;
BREITBURD, F ;
LEBRETON, C ;
HESLAN, M ;
DUBERTRET, L .
BRITISH JOURNAL OF DERMATOLOGY, 1986, 114 (01) :91-101
[10]   PHOTOSENSITIZERS - THERAPY AND DETECTION OF MALIGNANT-TUMORS [J].
DOUGHERTY, TJ .
PHOTOCHEMISTRY AND PHOTOBIOLOGY, 1987, 45 (06) :879-889