Connexin43 and Pannexin1 Channels in Osteoblasts: Who Is the "Hemichannel"?

被引:38
|
作者
Thi, Mia M. [1 ,2 ]
Islam, Shalena [4 ]
Suadicani, Sylvia O. [2 ,3 ]
Spray, David C. [2 ]
机构
[1] Albert Einstein Coll Med, Dept Orthoped Surg, Bronx, NY 10461 USA
[2] Albert Einstein Coll Med, Dept Neurosci, Bronx, NY 10461 USA
[3] Albert Einstein Coll Med, Dept Urol, Bronx, NY 10461 USA
[4] CUNY City Coll, Dept Biol, New York, NY 10031 USA
来源
JOURNAL OF MEMBRANE BIOLOGY | 2012年 / 245卷 / 07期
基金
美国国家卫生研究院;
关键词
P2X(7)R; ATP; Osteoblast; Gap junction; Dye uptake; GAP-JUNCTION HEMICHANNELS; ATP RELEASE; MEMBRANE CHANNELS; BONE-FORMATION; P2X(7); OSTEOCYTES; CELLS; COMMUNICATION; PORE; PHARMACOLOGY;
D O I
10.1007/s00232-012-9462-2
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
Osteoblasts sense and respond to mechanical stimuli in a process involving influx and release of large ions and signaling molecules. Unapposed gap junction hemichannels formed of connexin43 (Cx43) have been proposed as a major route for such exchange, in particular for release of ATP and prostaglandin E-2 (PGE(2)) in osteocytes. However, we have found that Cx43-null osteoblasts have unaltered, mechanically induced PGE(2) release and ATP-induced YoPro dye uptake. In contrast, PGE(2) release in response to fluid shear stress is abolished in P2X(7) receptor (P2X(7)R)-null osteoblasts, and ATP-induced dye uptake is attenuated following treatment of wild-type cells with a P2X(7)R or Pannexin1 (Panx1) channel blocker. These data indicate that Panx1 channels, in concert with P2X(7)R, likely form a molecular complex that performs the hemichannel function in osteoblast mechanosignaling.
引用
收藏
页码:401 / 409
页数:9
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