Methylene Blue-Mediated Photodynamic Therapy Induces Mitochondria-Dependent Apoptosis in HeLa Cell

被引:54
作者
Lu, Yan [1 ]
Jiao, Ruiqing [1 ]
Chen, Xiaoping [1 ]
Zhong, Jieying [1 ]
Ji, Jianguo [2 ]
Shen, Pingping [1 ]
机构
[1] Nanjing Univ, Sch Life Sci, State Key Lab Pharmaceut Biotechnol, Nanjing 210093, Peoples R China
[2] Peking Univ, Coll Life Sci, Proteome Grp Natl Lab Prot Engn & Plant Genet Eng, Beijing 100871, Peoples R China
关键词
APOPTOSIS; METHYLENE BLUE; HELA CELL; PHOTODYNAMIC THERAPY; MITOCHONDRIA PROTEOMICS;
D O I
10.1002/jcb.21965
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
Methylene blue (MB), a widely studied reagent, is investigated in this work for its usage in photodynamic therapy (PDT). PDT has been proved to be highly effective in the treatment of different types of cancers. Previous studies showed MB has both high affinity for mitochondria and high photodynamic efficiency. To elucidate the effects of MB in PDT, we analyzed PDT-induced apoptosis in HeLa cells by introducing different doses of MB into the culture media. Our data showed that MB-mediated PDT triggered intense apoptotic cell death through a series of steps, beginning with photochemical generation of reactive oxygen species. The release of cytochrome c and activation of caspase-3 indicated that MB-PDT-mediated apoptosis in HeLa cells was executed by the mitochondria-dependent apoptotic pathway. Importantly, proteomic studies confirmed that expression levels of several mitochondrial proteins were altered in MB-PDT-induced apoptosis, including TRAP1, mitochondrial elongation factor Tu and peroxiredoxin 3 isoform b. Western blot data showed that phosphorylation of ERK 1/2 and PKA were reduced in MB-PDT treated cells, indicating several signal molecules participating in this apoptotic cascade. Moreover, MB-PDT induced an increase in the strength of interaction between Bcl-xL and dephosphorylated Bad. This led to loss of the pro-survival function of Bcl-xL and resulted in mitochondria-mediated apoptosis. This study provides solid evidence of a strong induction by MB-PDT of a mitochondria-dependent apoptosis cascade in HeLa cells. J. Cell. Biochem. 105: 1451-1460, 2008. (C) 2008 Wilcy-Liss, Inc.
引用
收藏
页码:1451 / 1460
页数:10
相关论文
共 45 条
[1]   Intracellular signaling mechanisms in photodynamic therapy [J].
Almeida, RD ;
Manadas, BJ ;
Carvalho, AP ;
Duarte, CB .
BIOCHIMICA ET BIOPHYSICA ACTA-REVIEWS ON CANCER, 2004, 1704 (02) :59-86
[2]   The induction of apoptosis by a positively charged methylene blue derivative [J].
Ball, DJ ;
Luo, Y ;
Kessel, D ;
Griffiths, J ;
Brown, SB ;
Vernon, DI .
JOURNAL OF PHOTOCHEMISTRY AND PHOTOBIOLOGY B-BIOLOGY, 1998, 42 (02) :159-163
[3]  
BELLIN JS, 1961, CANCER RES, V21, P1365
[4]   Molecular effectors of multiple cell death pathways initiated by photodynamic therapy [J].
Buytaert, Esther ;
Dewaele, Michael ;
Agostinis, Patrizia .
BIOCHIMICA ET BIOPHYSICA ACTA-REVIEWS ON CANCER, 2007, 1776 (01) :86-107
[5]  
CARMEN G, 2004, CURR OPIN CELL BIOL, V16, P639
[6]   Peroxiredoxin III, a mitochondrion-specific peroxidase, regulates apoptotic signaling by mitochondria [J].
Chang, TS ;
Cho, CS ;
Park, S ;
Yu, SQ ;
Kang, SW ;
Rhee, SG .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2004, 279 (40) :41975-41984
[7]   Protein phosphatase 2A dephosphorylation of phosphoserine 112 plays the gatekeeper role for BAD-mediated apoptosis [J].
Chiang, CW ;
Kanies, C ;
Kim, KW ;
Fang, WB ;
Parkhurst, C ;
Xie, MH ;
Henry, T ;
Yang, E .
MOLECULAR AND CELLULAR BIOLOGY, 2003, 23 (18) :6350-6362
[8]   5-aminolaevulinic acid photodynamic therapy in a transgenic mouse model of skin melanoma [J].
Córdoba, F ;
Braathen, LR ;
Weissenberger, J ;
Vallan, C ;
Kato, M ;
Nakashima, I ;
Weis, J ;
von Felbert, V .
EXPERIMENTAL DERMATOLOGY, 2005, 14 (06) :429-437
[9]   The BCL2 family: Regulators of the cellular life-or-death switch [J].
Cory, S ;
Adams, JM .
NATURE REVIEWS CANCER, 2002, 2 (09) :647-656
[10]   Photodynamic therapy for cancer [J].
Dolmans, DEJGJ ;
Fukumura, D ;
Jain, RK .
NATURE REVIEWS CANCER, 2003, 3 (05) :380-387