The P2X7 receptor-pannexin connection to dye uptake and IL-1β release

被引:142
作者
Pelegrin, Pablo [1 ]
Surprenant, Annmarie [1 ]
机构
[1] Univ Manchester, Fac Life Sci, Manchester M13 9PT, Lancs, England
基金
英国生物技术与生命科学研究理事会; 英国惠康基金;
关键词
Caspase-1; Inflammasome; Dye uptake; Inflammation; Macrophage; TRANSFORMED MOUSE FIBROBLASTS; EXTRACELLULAR ATP; PLASMA-MEMBRANE; CASPASE-1; ACTIVATION; INTERLEUKIN-1-BETA RELEASE; NUCLEOTIDE PERMEABILITY; HUMAN-LYMPHOCYTES; PORE FORMATION; P-2Z RECEPTOR; EXTERNAL ATP;
D O I
10.1007/s11302-009-9141-7
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
The P2X(7) receptor (P2X(7)R) is uniquely associated with two distinct cellular responses: activation of a dye-permeable pathway allowing passage of molecules up to 900 Da and rapid release of the pro-inflammatory cytokine, interleukin-1 beta (IL-1 beta), from activated macrophage. How this dye uptake path forms and whether it is involved in IL-1 beta release has not been known. Pannexin-1 is a recently identified protein found to physically associate with the P2X(7)R. Inhibition of pannexin-1 does not alter P2X(7)R ion channel activation or associated calcium flux but blocks one component of P2X(7)R-induced dye uptake and unmasks a slower, previously undetected, dye uptake pathway. Inhibition of pannexin-1 blocks P2X(7)R-mediated IL-1 beta release from macrophage as well as release mediated by other stimuli which couple to activation of capase-1 and additionally inhibits the release of interleukin-1 alpha, a member of the IL-1 family whose processing does not require caspase-1 activation. Thus, pannexin-1 is linked to both dye uptake and IL-1 beta release but via distinct mechanisms.
引用
收藏
页码:129 / 137
页数:9
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