Functional expression of P2X family receptors in macrophages is affected by microenvironment in mouse T cell acute lymphoblastic leukemia

被引:12
作者
Chen, Shayan [1 ,2 ,3 ]
Feng, Wenli [1 ,2 ,3 ]
Yang, Xiao [1 ,2 ,3 ]
Yang, Wanzhu [1 ,2 ,3 ]
Ru, Yongxin [1 ,2 ,3 ]
Liao, Jinfeng [1 ,2 ,3 ]
Wang, Lina [1 ,2 ,3 ]
Lin, Yongmin [1 ,2 ,3 ]
Ren, Qian [1 ,2 ,3 ]
Zheng, Guoguang [1 ,2 ,3 ,4 ]
机构
[1] Chinese Acad Med Sci, Inst Hematol, State Key Lab Expt Hematol, Tianjin 300020, Peoples R China
[2] Chinese Acad Med Sci, Blood Dis Hosp, Tianjin 300020, Peoples R China
[3] Peking Union Med Coll, Tianjin 300020, Peoples R China
[4] Chinese Acad Med Sci, Ctr Stem Cell Med, Beijing 100730, Peoples R China
基金
中国国家自然科学基金;
关键词
Macrophage; Leukemia; P2X family receptors; Apoptosis; STRESS; INJURY; STEM; ATP;
D O I
10.1016/j.bbrc.2014.03.048
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
070307 [化学生物学]; 071010 [生物化学与分子生物学];
摘要
Nucleotides are important players in intercellular signaling communication network. P2X family receptors (P2XRs) are ATP-gated plasma membrane ion channels with diverse biological functions. Macrophages are important components in the microenvironment of hematopoiesis participating in both physiological and pathological processes. However, the role of P2XRs in macrophages in leukemia has not been established. Here we investigated expression pattern and functions of P2XR5 in macrophages from bone marrow (BM) and spleen of Notchl -induced T-ALL mice. Real-time PCR showed that P2XRs except P2X5R were expressed in BM and spleen macrophages. Furthermore, with the development of leukemia, the expression of P2X7R increased in both BM and spleen macrophages whereas expression of P2X1R increased in spleen macrophages. Live cell imaging recoding the Ca2+ response demonstrated that P2X7R expressed in macrophages was functional. TUNEL and electron microscopy analysis found that apoptotic macrophages were frequently observed in BM and spleen at late stage of leukemia, which was partly contributed by the activation of overexpressed P2X7R. Our results suggested that the intercellular communication mediated by nucleotides might orchestrate in the pathological process of leukemia and could be a potential target for the treatment of leukemia. (C) 2014 Elsevier Inc. All rights reserved.
引用
收藏
页码:1002 / 1009
页数:8
相关论文
共 36 条
[1]
P2X7 Receptor Function in Bone-Related Cancer [J].
Adinolfi, Elena ;
Amoroso, Francesca ;
Giuliani, Anna Lisa .
JOURNAL OF OSTEOPOROSIS, 2012, 2012
[2]
Alvaro T, 2006, HAEMATOLOGICA, V91, P1605
[3]
Purinergic signalling: past, present and future [J].
Burnstock, G. .
BRAZILIAN JOURNAL OF MEDICAL AND BIOLOGICAL RESEARCH, 2009, 42 (01) :3-8
[4]
Ca2+store depletion and endoplasmic reticulum stress are involved in P2X7 receptor-mediated neurotoxicity in differentiated NG108-15 cells [J].
Chao, Chia-Chia ;
Huang, Chieh-Chen ;
Lu, Dah-Yuu ;
Wong, Kar-Lok ;
Chen, Yun-Ru ;
Cheng, Tzu-Hurng ;
Leung, Yuk-Man .
JOURNAL OF CELLULAR BIOCHEMISTRY, 2012, 113 (04) :1377-1385
[5]
Modulation of P2X7 purinergic receptor in macrophages by Leishmania amazonensis and its role in parasite elimination [J].
Chaves, Suzana Passos ;
Torres-Santos, Eduardo Caio ;
Marques, Camila ;
Figliuolo, Vanessa Ribeiro ;
Persechini, Pedro Muanis ;
Coutinho-Silva, Robson ;
Rossi-Bergmann, Bartira .
MICROBES AND INFECTION, 2009, 11 (10-11) :842-849
[6]
Regulation of immune response by P2X7 receptor [J].
Chen, Lanfen ;
Brosnan, Celia F. .
CRITICAL REVIEWS IN IMMUNOLOGY, 2006, 26 (06) :499-513
[7]
Spontaneous cell fusion in macrophage cultures expressing high levels of the P2Z/P2X(7) receptor [J].
Chiozzi, P ;
Sanz, JM ;
Ferrari, D ;
Falzoni, S ;
Aleotti, A ;
Buell, GN ;
Collo, G ;
DiVirgilio, F .
JOURNAL OF CELL BIOLOGY, 1997, 138 (03) :697-706
[8]
The hyposensitive N187D P2X7 mutant promotes malignant progression in nude mice [J].
Chong J.-H. ;
Zheng G.-G. ;
Ma Y.-Y. ;
Zhang H.-Y. ;
Nie K. ;
Lin Y.-M. ;
Wu K.-F. .
Journal of Biological Chemistry, 2010, 285 (46) :36179-36187
[9]
Abnormal expression of P2X family receptors in Chinese pediatric acute leukemias [J].
Chong, Jing-Hui ;
Zheng, Guo-Guang ;
Zhu, Xiao-Fan ;
Guo, Ye ;
Wang, Lin ;
Ma, Cui-Hua ;
Liu, Shu-Yan ;
Xu, Lin-Lin ;
Lin, Yong-Min ;
Wu, Ke-Fu .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 2010, 391 (01) :498-504
[10]
Bone marrow CD169+ macrophages promote the retention of hematopoietic stem and progenitor cells in the mesenchymal stem cell niche [J].
Chow, Andrew ;
Lucas, Daniel ;
Hidalgo, Andres ;
Mendez-Ferrer, Simon ;
Hashimoto, Daigo ;
Scheiermann, Christoph ;
Battista, Michela ;
Leboeuf, Marylene ;
Prophete, Colette ;
van Rooijen, Nico ;
Tanaka, Masato ;
Merad, Miriam ;
Frenette, Paul S. .
JOURNAL OF EXPERIMENTAL MEDICINE, 2011, 208 (02) :261-271