Peroxisome proliferator-activated receptor γ-regulated ABCG2 expression confers cytoprotection to human dendritic cells

被引:146
作者
Szatmari, Istvan
Vamosi, Gyoergy
Brazda, Peter
Balint, Balint L.
Benko, Szilvia
Szeles, Lajos
Jeney, Viktoria
Oezvegy-Laczka, Csilla
Szanto, Attila
Barta, Endre
Balla, Jozsef
Balazs Sarkadi
Nagy, Laszlo
机构
[1] Hungarian Acad Sci, Dept Biochem & Mol Biol, H-4032 Debrecen, Hungary
[2] Hungarian Acad Sci, Cell Biophys Res Grp, H-4032 Debrecen, Hungary
[3] Univ Debrecen, Dept Immunol, H-4032 Debrecen, Hungary
[4] Univ Debrecen, Dept Internal Med, Res Ctr Mol Med, Med & Hlth Sci Ctr, H-4032 Debrecen, Hungary
[5] Hungarian Acad Sci, Membrane Res Grp, Inst Haematol & Immunol, Natl Med Ctr, H-1113 Budapest, Hungary
[6] Ctr Agr Biotechnol, H-2100 Godollo, Hungary
基金
英国惠康基金;
关键词
D O I
10.1074/jbc.M604890200
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
ABCG2, a member of the ATP-binding cassette transporters has been identified as a protective pump against endogenous and exogenous toxic agents. ABCG2 was shown to be expressed at high levels in stem cells and variably regulated during cell differentiation. Here we demonstrate that functional ABCG2 is expressed in human monocyte-derived dendritic cells by the activation of a nuclear hormone receptor, PPAR gamma. We identified and characterized a 150-base pair long conserved enhancer region, containing three functional PPAR response elements (PPARE), upstream of the human ABCG2 gene. We confirmed the binding of the PPAR gamma(.) RXR heterodimer to this enhancer region, suggesting that PPAR gamma directly regulates the transcription of ABCG2. Consistent with these results, elevated expression of ABCG2 mRNA was coupled to enhanced protein production, resulting in increased xenobiotic extrusion capacity via ABCG2 in PPAR gamma-activated cells. Furthermore PPAR gamma instructed dendritic cells showed increased Hoechst dye extrusion and resistance to mitoxantrone. Collectively, these results uncovered a mechanism by which up-regulation of functional ABCG2 expression can be achieved via exogenous or endogenous activation of the lipid-activated transcription factor, PPAR gamma. The increased expression of the promiscuous ABCG2 transporter can significantly modify the xenobiotic and drug resistance of human myeloid dendritic cells.
引用
收藏
页码:23812 / 23823
页数:12
相关论文
共 35 条
[31]   Transcriptional regulation of human CYP27 integrates retinoid, peroxisome proliferator-activated receptor, and liver X receptor signaling in macrophages [J].
Szanto, A ;
Benko, S ;
Szatmari, I ;
Balint, BL ;
Furtos, I ;
Rühl, R ;
Molnar, S ;
Csiba, L ;
Garuti, R ;
Calandra, S ;
Larsson, H ;
Diczfalusy, U ;
Nagy, L .
MOLECULAR AND CELLULAR BIOLOGY, 2004, 24 (18) :8154-8166
[32]   Activation of PPARγ specifies a dendritic cell subtype capable of enhanced induction of iNKT cell expansion [J].
Szatmari, I ;
Gogolak, P ;
Im, JS ;
Dezso, B ;
Rajnavolgyi, E ;
Nagy, L .
IMMUNITY, 2004, 21 (01) :95-106
[33]   Peroxisome proliferator-activated receptor γ and metabolic disease [J].
Willson, TM ;
Lambert, MH ;
Kliewer, SA .
ANNUAL REVIEW OF BIOCHEMISTRY, 2001, 70 :341-367
[34]   The ABC transporter Bcrp1/ABCG2 is expressed in a wide variety of stem cells and is a molecular determinant of the side-population phenotype [J].
Zhou, S ;
Schuetz, JD ;
Bunting, KD ;
Colapietro, AM ;
Sampath, J ;
Morris, JJ ;
Lagutina, I ;
Grosveld, GC ;
Osawa, M ;
Nakauchi, H ;
Sorrentino, BP .
NATURE MEDICINE, 2001, 7 (09) :1028-1034
[35]  
ZHOU S, 2004, BLOOD