Basal activation of the P2X7 ATP receptor elevates mitochondrial calcium and potential, increases cellular ATP levels, and promotes serum-independent growth

被引:238
作者
Adinolfi, E [1 ]
Callegari, MG [1 ]
Ferrari, D [1 ]
Bolognesi, C [1 ]
Minelli, M [1 ]
Wieckowski, MR [1 ]
Pinton, P [1 ]
Rizzuto, R [1 ]
Di Virgilio, F [1 ]
机构
[1] Univ Ferrara, Ctr Study Inflammat, Dept Expt & Diagnost Med, Sect Gen Pathol & Interdisciplinary, I-44100 Ferrara, Italy
关键词
D O I
10.1091/mbc.E04-11-1025
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
P2X(7) is a bifunctional receptor (P2X(7)R) for extracellular ATP that, depending on the level of activation, forms a cation-selective channel or a large conductance nonselective pore. The P2X7R has a strong proapoptotic activity but can also support growth. Here, we describe the mechanism involved in growth stimulation. Transfection of P2X(7)R increases resting mitochondrial potential (Delta psi(mt)), basal mitochondrial Ca2+([Ca2+](mt)), intracellular ATP content, and confers ability to grow in the absence of serum. These changes require a full pore-forming function, because they are abolished in cells transfected with a mutated P2X(7)R that retains channel activity but cannot form the nonselective pore, and depend on an autocrine/paracrine tonic stimulation by secreted ATP. On the other hand, sustained stimulation of P2X(7)R causes a Delta psi(mt) drop, a large increase in [Ca2+](mt), mitochondrial fragmentation, and cell death. These findings reveal a hitherto undescribed mechanism for growth stimulation by a plasma membrane pore.
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收藏
页码:3260 / 3272
页数:13
相关论文
共 30 条
[1]   Tyrosine phosphorylation of HSP90 within the P2X7 receptor complex negatively regulates P2X7 receptors [J].
Adinolfi, E ;
Kim, M ;
Young, MT ;
Di Virgilio, F ;
Surprenant, A .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2003, 278 (39) :37344-37351
[2]   P2X7 receptor expression in evolutive and indolent forms of chronic B lymphocytic leukemia [J].
Adinolfi, E ;
Melchiorni, L ;
Falzoni, S ;
Chiozzi, P ;
Morelli, A ;
Tieghi, A ;
Cuneo, A ;
Castoldi, G ;
Di Virgilio, F ;
Baricordi, OR .
BLOOD, 2002, 99 (02) :706-708
[3]   Increased proliferation rate of lymphoid cells transfected with the P2X7 ATP receptor [J].
Baricordi, OR ;
Melchiorri, L ;
Adinolfi, E ;
Falzoni, S ;
Chiozzi, P ;
Buell, G ;
Di Virgilio, F .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1999, 274 (47) :33206-33208
[4]   A mitochondrial perspective on cell death [J].
Bernardi, P ;
Petronilli, V ;
Di Lisa, F ;
Forte, M .
TRENDS IN BIOCHEMICAL SCIENCES, 2001, 26 (02) :112-117
[5]   Purinergic signaling and vascular cell proliferation and death [J].
Burnstock, G .
ARTERIOSCLEROSIS THROMBOSIS AND VASCULAR BIOLOGY, 2002, 22 (03) :364-373
[6]   Human mitochondrial thioredoxin -: Involvement in mitochondrial membrane potential and cell death [J].
Damdimopoulos, AE ;
Miranda-Vizuete, A ;
Pelto-Huikko, M ;
Gustafsson, JÅ ;
Spyrou, G .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2002, 277 (36) :33249-33257
[7]   ON THE ROLE OF THE CALCIUM-TRANSPORT CYCLE IN HEART AND OTHER MAMMALIAN MITOCHONDRIA [J].
DENTON, RM ;
MCCORMACK, JG .
FEBS LETTERS, 1980, 119 (01) :1-8
[8]   Nucleotide receptors: an emerging family of regulatory molecules in blood cells [J].
Di Virgilio, F ;
Chiozzi, P ;
Ferrari, D ;
Falzoni, S ;
Sanz, JM ;
Morelli, A ;
Torboli, M ;
Bolognesi, G ;
Baricordi, OR .
BLOOD, 2001, 97 (03) :587-600
[9]   THE P2Z PURINOCEPTOR - AN INTRIGUING ROLE IN IMMUNITY, INFLAMMATION AND CELL-DEATH [J].
DIVIRGILIO, F .
IMMUNOLOGY TODAY, 1995, 16 (11) :524-528
[10]  
Duchen MR, 2003, METHOD ENZYMOL, V361, P353