Enzyme-assisted photosensitization with rose Bengal acetate induces structural and functional alteration of mitochondria in HeLa cells

被引:21
作者
Bottone, M. G.
Soldani, C.
Fraschini, A.
Alpini, C.
Croce, A. C.
Bottiroli, G.
Pellicciari, C.
机构
[1] Univ Pavia, Dipartimento Biol Anim, I-27100 Pavia, Italy
[2] CNR, IGM, Sez Istochim & Citometria, I-27100 Pavia, Italy
[3] IRCCS San Matteo, Lab Anal Biochim Clin, Pavia, Italy
关键词
rose Bengal acetate; photodamage; mitochondria; fluorescence microscopy; electron microscopy; cytometry;
D O I
10.1007/s00418-006-0235-9
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Rose Bengal acetate (RB-Ac) can be used as a fluorogenic substrate for photosensitization of cells both in vivo and in vitro: once inside the cells, RB-Ac is converted into photoactive rose Bengal (RB) molecules which redistribute dynamically in the cytoplasm and, upon irradiation by visible green light, can damage organelles such as the endoplasmic reticulum, the Golgi apparatus, and the cytoskeleton. Recently, evidence has been provided that mitochondria may also be affected. The aims of the present study were to describe RB-induced photodamage of mitochondria in single HeLa cells and to define, on a quantitative basis, the effects of photosensitization on their morphofunctional features. HeLa cell cultures were exposed to 10(-5) M RB-Ac for 60 min and then irradiated with a light emitting diode at 530 nm (total light dose, 1.6 J/cm(2)). After irradiation, the cells were transferred to a drug-free complete medium and allowed to grow for 24-72 h. Using conventional and confocal fluorescence microscopy, transmission electron microscopy, and flow cytometry, we demonstrate that, in photosensitized cells, mitochondria undergo structural and functional alterations which can lead cells to apoptosis. Interestingly, in our system some cells were able to survive 72 h post-treatment and to recover, exhibiting the same mitochondrial structure, distribution and inner membrane potential as those in untreated controls. Taking into account that the photoactive molecules redistribute dynamically inside the cell upon RB-Ac administration, it may be hypothesized that cells can be differently affected by irradiation, depending on the relative amount and organelle location of the photosensitizer.
引用
收藏
页码:263 / 271
页数:9
相关论文
共 38 条
[11]   Release of cytochrome c, Bax migration, Bid cleavage, and activation of caspases 2, 3, 6, 7, 8, and 9 during endothelial cell apoptosis [J].
Granville, DJ ;
Shaw, JR ;
Leong, S ;
Carthy, CM ;
Margaron, P ;
Hunt, DW ;
McManus, BM .
AMERICAN JOURNAL OF PATHOLOGY, 1999, 155 (04) :1021-1025
[12]   Mitochondria-dependent apoptosis induced by a novel amphipathic photochemotherapeutic agent ZnPcS2P2 in HL60 cells [J].
Huang, HF ;
Chen, YZ ;
Wu, Y .
ACTA PHARMACOLOGICA SINICA, 2005, 26 (09) :1138-1144
[13]  
Kessel D, 2000, PHOTOCHEM PHOTOBIOL, V71, P196, DOI 10.1562/0031-8655(2000)071<0196:DOTART>2.0.CO
[14]  
2
[15]   Photodynamic therapy: A mitochondrial inducer of apoptosis [J].
Kessel, D ;
Luo, Y .
CELL DEATH AND DIFFERENTIATION, 1999, 6 (01) :28-35
[16]   Initiation of apoptosis and autophagy by photodynamic therapy [J].
Kessel, David ;
Vicente, M. Graca H. ;
Reiners, John J., Jr. .
LASERS IN SURGERY AND MEDICINE, 2006, 38 (05) :482-488
[17]   Classification of cell death: recommendations of the Nomenclature Committee on Cell Death [J].
Kroemer, G ;
El-Deiry, W ;
Golstein, P ;
Peter, ME ;
Vaux, D ;
Vandenabeele, P ;
Zhivotovsky, B ;
Blagosklonny, MV ;
Malorni, W ;
Knight, RA ;
Piacentini, M ;
Nagata, S ;
Melino, G .
CELL DEATH AND DIFFERENTIATION, 2005, 12 (Suppl 2) :1463-1467
[18]   Oxidative stress-induced depolymerization of microtubules and alteration of mitochondrial mass in human cells [J].
Lee, CF ;
Liu, CY ;
Hsieh, RH ;
Wei, YH .
ROLE OF THE MITOCHONDRIA IN HUMAN AGING AND DISEASE: FROM GENES TO CELL SIGNALING, 2005, 1042 :246-254
[19]   Melatonin prevents apoptosis induced by UV-B treatment in U937 cell line [J].
Luchetti, F ;
Canonico, B ;
Curci, R ;
Battistelli, M ;
Mannello, F ;
Papa, S ;
Tarzia, G ;
Falcieri, E .
JOURNAL OF PINEAL RESEARCH, 2006, 40 (02) :158-167
[20]   Chimeric forms of furin and TGN38 are transported from the plasma membrane to the trans-Golgi network via distinct endosomal pathways [J].
Mallet, WG ;
Maxfield, FR .
JOURNAL OF CELL BIOLOGY, 1999, 146 (02) :345-359