共 59 条
Regulation of Piezo Channels by Cellular Signaling Pathways
被引:27
作者:

Borbiro, I.
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机构:
Rutgers New Jersey Med Sch, Newark, NJ 07103 USA Rutgers New Jersey Med Sch, Newark, NJ 07103 USA

Rohacs, T.
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h-index: 0
机构:
Rutgers New Jersey Med Sch, Newark, NJ 07103 USA Rutgers New Jersey Med Sch, Newark, NJ 07103 USA
机构:
[1] Rutgers New Jersey Med Sch, Newark, NJ 07103 USA
来源:
PIEZO CHANNELS
|
2017年
/
79卷
关键词:
ACTIVATED ION-CHANNEL;
CAPSAICIN RECEPTOR;
PHOSPHOINOSITIDE REGULATION;
TRPV1;
MECHANOTRANSDUCTION;
MUTATIONS;
PAIN;
PHOSPHORYLATION;
DETERMINANTS;
POTENTIATION;
D O I:
10.1016/bs.ctm.2016.10.002
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 recently identified mechanically activated Piezo1 and Piezo2 channels play major roles in various aspects of mechanosensation in mammals, and their mutations are associated with human diseases. Recent reports show that activation of cell surface receptors coupled to heterotrimeric Gq proteins increase the sensitivity of Piezo2 channels to mechanical stimuli. Activation of the cyclic adenosine monophosphate pathway was also shown to potentiate Piezo2 channel activity. This phenomenon may play a role in mechanical allodynia or hyperalgesia during inflammation. Both Piezo1 and Piezo2 channels are inhibited upon depletion of plasma membrane phosphoinositides, in response to phospholipase C activation by Ca2+ influx via the transient receptor potential vanilloid 1 channels. This review will discuss current knowledge on regulation of Piezo channels by these intracellular signaling pathways.
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收藏
页码:245 / 261
页数:17
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共 59 条
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