P2X7 receptors: role in bone cell formation and function

被引:65
作者
Agrawal, Ankita [1 ]
Gartland, Alison [1 ]
机构
[1] Univ Sheffield, Mellanby Ctr Bone Res, Dept Human Metab, Sheffield S10 2RX, S Yorkshire, England
基金
欧盟第七框架计划;
关键词
apoptosis; bone; cancer; osteoblast; osteoclast; P2X7; PROTEIN-COUPLED RECEPTOR; NF-KAPPA-B; P2X(7) RECEPTOR; EXTRACELLULAR NUCLEOTIDES; PURINERGIC RECEPTORS; ATP RELEASE; IN-VITRO; OSTEOGENIC DIFFERENTIATION; OSTEOCLAST SURVIVAL; ADENINE RECEPTORS;
D O I
10.1530/JME-14-0226
中图分类号
R5 [内科学];
学科分类号
100201 [内科学];
摘要
The role of the P2X7 receptor (P2X7R) is being explored with intensive interest in the context of normal bone physiology, bone-related diseases and, to an extent, bone cancer. In this review, we cover the current understanding of P2X7R regulation of bone cell formation, function and survival. We will discuss how the P2X7R drives lineage commitment of undifferentiated bone cell progenitors, the vital role of P2X7R activation in bone mineralisation and its relatively unexplored role in osteocyte function. We also review how P2X7R activation is imperative for osteoclast formation and its role in bone resorption via orchestrating osteoclast apoptosis. Variations in the gene for the P2X7R (P2RX7) have implications for P2X7R-mediated processes and we review the relevance of these genetic variations in bone physiology. Finally, we highlight how targeting P2X7R may have therapeutic potential in bone disease and cancer.
引用
收藏
页码:R75 / R88
页数:14
相关论文
共 128 条
[1]
Basal activation of the P2X7 ATP receptor elevates mitochondrial calcium and potential, increases cellular ATP levels, and promotes serum-independent growth [J].
Adinolfi, E ;
Callegari, MG ;
Ferrari, D ;
Bolognesi, C ;
Minelli, M ;
Wieckowski, MR ;
Pinton, P ;
Rizzuto, R ;
Di Virgilio, F .
MOLECULAR BIOLOGY OF THE CELL, 2005, 16 (07) :3260-3272
[2]
P2X7 Receptor Function in Bone-Related Cancer [J].
Adinolfi, Elena ;
Amoroso, Francesca ;
Giuliani, Anna Lisa .
JOURNAL OF OSTEOPOROSIS, 2012, 2012
[3]
Expression of P2X7 Receptor Increases In Vivo Tumor Growth [J].
Adinolfi, Elena ;
Raffaghello, Lizzia ;
Giuliani, Anna Lisa ;
Cavazzini, Luigi ;
Capece, Marina ;
Chiozzi, Paola ;
Bianchi, Giovanna ;
Kroemer, Guido ;
Pistoia, Vito ;
Di Virgilio, Francesco .
CANCER RESEARCH, 2012, 72 (12) :2957-2969
[4]
Trophic activity of a naturally occurring truncated isoform of the P2X7 receptor [J].
Adinolfi, Elena ;
Cirillo, Maria ;
Woltersdorf, Ronja ;
Falzoni, Simonetta ;
Chiozzi, Paola ;
Pellegatti, Patrizia ;
Callegari, Maria Giulia ;
Sandona, Doriana ;
Markwardt, Fritz ;
Schmalzing, Guenther ;
Di Virgilio, Francesco .
FASEB JOURNAL, 2010, 24 (09) :3393-3404
[5]
Expression of the P2X7 Receptor Increases the Ca2+ Content of the Endoplasmic Reticulum, Activates NFATc1, and Protects from Apoptosis [J].
Adinolfi, Elena ;
Callegari, Maria Giulia ;
Cirillo, Maria ;
Pinton, Paolo ;
Giorgi, Carlotta ;
Cavagna, Dario ;
Rizzuto, Rosario ;
Di Virgilio, Francesco .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2009, 284 (15) :10120-10128
[6]
Cutting edge: A natural P451L mutation in the cytoplasmic domain impairs the function of the mouse P2X7 receptor [J].
Adriouch, S ;
Dox, C ;
Welge, V ;
Seman, M ;
Koch-Nolte, F ;
Haag, F .
JOURNAL OF IMMUNOLOGY, 2002, 169 (08) :4108-4112
[7]
Expression of NFATc1 is inducible by P2X7 receptor activation in human osteoclasts [J].
Agrawal, A. ;
Gartland, A. .
BONE, 2011, 48 :S126-S126
[8]
The effects of P2X7 receptor antagonists on the formation and function of human osteoclasts in vitro [J].
Agrawal, Ankita ;
Buckley, Katherine A. ;
Bowers, Keith ;
Furber, Mark ;
Gallagher, James A. ;
Gartland, Alison .
PURINERGIC SIGNALLING, 2010, 6 (03) :307-315
[9]
P2X7 receptor gene polymorphism analysis in rheumatoid arthritis [J].
Al-Shukaili, A. ;
Al-Kaabi, J. ;
Hassan, B. ;
Al-Araimi, T. ;
Al-Tobi, M. ;
Al-Kindi, M. ;
Al-Maniri, A. ;
Al-Gheilani, A. ;
Al-Ansari, A. .
INTERNATIONAL JOURNAL OF IMMUNOGENETICS, 2011, 38 (05) :389-396
[10]
Atypical P2X7 receptor pharmacology in two human osteoblast-like cell lines [J].
Alqallaf, S. M. ;
Evans, B. A. J. ;
Kidd, E. J. .
BRITISH JOURNAL OF PHARMACOLOGY, 2009, 156 (07) :1124-1135