Photosensitized rose Bengal-induced phototoxicity on human melanoma cell line under natural sunlight exposure

被引:24
|
作者
Srivastav, Ajeet K. [1 ]
Mujtaba, Syed Faiz [1 ]
Dwivedi, Ashish [1 ]
Amar, Saroj K. [1 ,3 ]
Goyal, Shruti [1 ,3 ]
Verma, Ankit [1 ]
Kushwaha, Hari N. [1 ]
Chaturvedi, Rajnish K. [2 ,3 ]
Ray, Ratan Singh [1 ,3 ]
机构
[1] Indian Inst Toxicol Res, CSIR, Photobiol Lab, Syst Toxicol & Hlth Risk Assessment Grp, POB 80,MG Marg, Lucknow 226001, Uttar Pradesh, India
[2] Indian Inst Toxicol Res, CSIR, Dev Toxicol Lab, Syst Toxicol & Hlth Risk Assessment Grp, POB 80,MG Marg, Lucknow 226001, Uttar Pradesh, India
[3] CSIR, Acad Sci & Innovat Res, IITR Campus, Lucknow, Uttar Pradesh, India
关键词
Rose Bengal; Melanoma cells; Singlet oxygen; DNA damage; Apoptosis; SINGLET OXYGEN; MITOCHONDRIAL DEPOLARIZATION; APOPTOSIS; UV; DAMAGE; CANCER; REPAIR; ASSAY;
D O I
10.1016/j.jphotobiol.2015.12.001
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
Rose Bengal (RB) is an anionic water-soluble xanthene dye, which used for many years to assess eye cornea and conjunctiva damage. RB showed strong absorption maxima (lambda(max)) under visible light followed by UV-B and UV-A. RB under sunlight exposure showed a time-dependent photodegradation. Our results show that photosensitized RB generates O-1(2) via Type-II photodynamic pathway and induced DNA damage under sunlight/UV-R exposure. 2'dGu0 degradation, micronuclei formation, and single- and double-strand breakage were the outcome of photogenotoxicity caused by RB. Quenching studies with NaN3 advocate the involvement of O-1(2) in RB photogenotoxicity. RB induced linoleic acid photoperoxidation, which was parallel to O-1(2) mediated DNA damage. Oxidative stress in A375 cell line (human melanoma cell line) was detected through DCF-DA assay. Photosensitized RB decreased maximum cellular viability under sunlight followed by UV-B and UV-A exposures. Apoptosis was detected as a pattern of cell death through the increased of caspase-3 activity, decreased mitochondrial membrane potential, and PS translocation through inner to outer plasma membrane. Increased cytosolic levels of Bax also advocate the apoptotic cell death. We propose a p53-mediated apoptosis via increased expression of Bax gene and protein. Thus, the exact mechanism behind RB phototoxicity was the involvement of O-1(2), which induced oxidative stress-mediated DNA and membrane damage, finally apoptotic cell death under natural sunlight exposure. The study suggests that after the use of RB, sunlight exposure may avoid to prevent from its harmful effects. (C) 2015 Published by Elsevier B.V.
引用
收藏
页码:87 / 99
页数:13
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