Vesicle disruption, plasma membrane bleb formation, and acute cell death caused by illumination with blue light in acridine orange-loaded malignant melanoma cells

被引:23
作者
Hiruma, Hiromi
Katakura, Takashi
Takenami, Tamie
Igawa, Satoshi
Kanoh, Maho
Fujimura, Takao
Kawakami, Tadashi
机构
[1] Kitasato Univ, Sch Med, Dept Physiol, Sagamihara, Kanagawa 2288555, Japan
[2] Kitasato Univ, Sch Med, Dept Anesthesiol, Sagamihara, Kanagawa 2288555, Japan
[3] Kitasato Univ, Sch Med, Dept Internal Med Resp Dis & Collagen Dis, Sagamihara, Kanagawa 2288555, Japan
[4] Kitasato Univ, Sch Med, Dept Dermatol, Sagamihara, Kanagawa 2288555, Japan
基金
日本学术振兴会;
关键词
acridine orange; acute cell death; malignant melanoma cells; plasma membrane blebs; vacuolar H+-ATPase; vesicle disruption;
D O I
10.1016/j.jphotobiol.2006.08.003
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
Acridine orange (AO), a weakly basic fluorescent dye, is permeable to plasma and vesicle membranes and preferentially remains in intracellular acidic regions. Using fluorescence microscopy, we observed dynamic changes in AO-loaded cultured malignant melanoma cells during illumination with blue light. Immediately after the start of the illumination, the successive disruption of vesicles was observed as a flash of fluorescence, and shortly after that, blebs were formed on the plasma membrane. These cells died within 5 min. Vesicle disruption was completely inhibited when cells were treated with the Vacuolar H+-ATPase inhibitor bafilomycin A] followed by loading with AO, but not when bafilomycin A I was treated after AO loading. Thus, the filling of AO in the vesicle, which is driven by vacuolar H+-ATPase, is initially required for vesicle disruption. In contrast, bafilomycin Al did not prevent plasma membrane blebbing, indicating that the blebs are formed independently of the vesicle disruption. Acute cell death was inhibited by treatment with bafilomycin Al before but not after AO loading. Thus, AO- and blue light-induced acute cell death is associated with vesicle disruption rather than bleb formation. Both the vesicle disruption and the formation of plasma membrane blebs were inhibited by removal of oxygen from the cell environment and by singlet oxygen scavengers, sodium azide, ascorbic acid, and L-histidine, but not inhibited by the hydroxyl radical scavenger dimethyl thiourea. Acute cell death was also prevented by singlet oxygen scavengers but not by dimethyl thiourea. Thus, these phenomena are likely caused at least in part by the generation of singlet oxygen. The photosensitive features of plasma and vesicle membranes observed in the present study may be based on the use of the photodynamic effect, such as cancer therapy. (c) 2006 Elsevier B.V. All rights reserved.
引用
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页码:1 / 8
页数:8
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