Expression and function of the P2X7 receptor in rat C6 glioma cells

被引:84
作者
Wei, Wei [1 ]
Ryu, Jae K. [1 ]
Choi, Hyun B. [1 ]
McLarnon, James G. [1 ]
机构
[1] Univ British Columbia, Fac Med, Dept Anesthesia Pharmacol & Therapeut, Vancouver, BC V6T 1Z3, Canada
关键词
rat c6 glioma cells; P2X(7) receptor; calcium imaging; migration; BzATP; OxATP;
D O I
10.1016/j.canlet.2007.10.025
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Our results demonstrate the first findings of expression and function of the purinergic P2X(7) receptor (P2X(7)R) in rat C6 glioma cells. P2X(7)R mRNA and protein were present in unstimulated C6 cells and were up-regulated by cell exposure to the P2X(7)R agonist, 2',3'-(benzoyl-4-benzoyl)-ATP (BzATP). Activation of P2X(7)R in C6 in response to BzATP led to increased mobilization of intracellular calcium [Ca2+]i and formation of large pores. Chronic exposure of C6 cells to BzATP enhanced the expression of pro-inflammatory factors including MCP-1, IL-8 and VEGF. In a scratch-wound migration assay, the P2X(7)R was shown to regulate cell mobility. The overall results suggest that P2X(7)R activation in C6 is linked with increased pro-inflammatory factors and tumor cell migration. (C) 2007 Elsevier Ireland Ltd. All rights reserved.
引用
收藏
页码:79 / 87
页数:9
相关论文
共 50 条
[31]   C6 GLIOMA CELL INVASION AND MIGRATION OF RAT-BRAIN AFTER NEURAL HOMOGRAFTING - ULTRASTRUCTURE [J].
BERNSTEIN, JJ ;
GOLDBERG, WJ ;
LAWS, ER ;
CONGER, D ;
MORREALE, V ;
WOOD, LR .
NEUROSURGERY, 1990, 26 (04) :622-628
[32]   P2X7 receptor activation enhances SK3 channels- and cystein cathepsin-dependent cancer cells invasiveness [J].
Jelassi, B. ;
Chantome, A. ;
Alcaraz-Perez, F. ;
Baroja-Mazo, A. ;
Cayuela, M. L. ;
Pelegrin, P. ;
Surprenant, A. ;
Roger, S. .
ONCOGENE, 2011, 30 (18) :2108-2122
[33]   P2X7 receptor activation enhances SK3 channels- and cystein cathepsin-dependent cancer cells invasiveness [J].
B Jelassi ;
A Chantôme ;
F Alcaraz-Pérez ;
A Baroja-Mazo ;
M L Cayuela ;
P Pelegrin ;
A Surprenant ;
S Roger .
Oncogene, 2011, 30 :2108-2122
[34]   Temozolomide inhibits cellular growth and motility via targeting ERK signaling in glioma C6 cells [J].
Wang, Yingge ;
Gao, Shan ;
Wang, Weiguang ;
Liang, Jingyan .
MOLECULAR MEDICINE REPORTS, 2016, 14 (06) :5732-5738
[35]   Effects of Recombinant Disintegrin rAdinbitor on FAK-Ras/MAPK Pathway in C6 Glioma Cells [J].
Zhao Ting ;
Li Jin-Ping ;
Hu Yan-Rong ;
Hong Yan ;
Zhao Bao-Chang .
PROGRESS IN BIOCHEMISTRY AND BIOPHYSICS, 2009, 36 (06) :702-708
[36]   Chlorogenic Acid in Viscum album Callus is a Potential Anticancer Agent against C6 Glioma Cells [J].
Kim, Jinwoo ;
Baek, Suji ;
Lee, Kang Pa ;
Moon, Byung Seok ;
Kim, Hyun-Soo ;
Kwon, Seung-Hae ;
Lee, Dae Won ;
Kim, Jisu .
PHARMACOGNOSY MAGAZINE, 2020, 16 (71) :531-537
[37]   Alkannin inhibits growth and invasion of glioma cells C6 through IQGAP/mTOR signal pathway [J].
Gao, Chunyan ;
Liang, Cunyin ;
Nie, Zhengui ;
Liu, Ying ;
Wang, Junya ;
Zhang, Dongmei .
INTERNATIONAL JOURNAL OF CLINICAL AND EXPERIMENTAL MEDICINE, 2015, 8 (04) :5287-5294
[38]   Microtubular Assessment of C6 Rat Glioma Cell Spheroids Developed in Transparent Liquid Marbles or Hanging Drops [J].
Langella, Arianna ;
Gadau, Sergio Domenico ;
Serra, Elisa ;
Bebbere, Daniela ;
Ledda, Sergio .
BIOLOGY-BASEL, 2022, 11 (04)
[39]   P2X7 Receptor Promotes Mouse Mammary Cancer Cell Invasiveness and Tumour Progression, and Is a Target for Anticancer Treatment [J].
Brisson, Lucie ;
Chadet, Stephanie ;
Lopez-Charcas, Osbaldo ;
Jelassi, Bilel ;
Ternant, David ;
Chamouton, Julie ;
Lerondel, Stephanie ;
Le Pape, Alain ;
Couillin, Isabelle ;
Gombault, Aurelie ;
Trovero, Fabrice ;
Chevalier, Stephan ;
Besson, Pierre ;
Jiang, Lin-Hua ;
Roger, Sebastien .
CANCERS, 2020, 12 (09) :1-23
[40]   Abnormal expression of homeobox c6 in the atherosclerotic aorta and its effect on proliferation and migration of rat vascular smooth muscle cells [J].
Long, Xiangshu ;
You, Ganhua ;
Wu, Qiang ;
Zhou, Yu ;
Yu, Fuxun ;
Xiao, Yan ;
Deng, Shiyan ;
Song, Fang ;
Huang, Jing ;
Tian, Maobo .
ACTA BIOCHIMICA ET BIOPHYSICA SINICA, 2020, 52 (09) :935-943