Transient receptor potential TRPA1 channel desensitization in sensory neurons is agonist dependent and regulated by TRPV1-directed internalization
被引:225
作者:
Akopian, Armen N.
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机构:Univ Texas, Hlth Sci Ctr, Dept Endodont, San Antonio, TX 78229 USA
Akopian, Armen N.
Ruparel, Nikita B.
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机构:Univ Texas, Hlth Sci Ctr, Dept Endodont, San Antonio, TX 78229 USA
Ruparel, Nikita B.
Jeske, Nathaniel A.
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机构:Univ Texas, Hlth Sci Ctr, Dept Endodont, San Antonio, TX 78229 USA
Jeske, Nathaniel A.
Hargreaves, Kenneth M.
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机构:Univ Texas, Hlth Sci Ctr, Dept Endodont, San Antonio, TX 78229 USA
Hargreaves, Kenneth M.
机构:
[1] Univ Texas, Hlth Sci Ctr, Dept Endodont, San Antonio, TX 78229 USA
[2] Univ Texas, Hlth Sci Ctr, Dept Cellular & Struct Biol, San Antonio, TX 78229 USA
[3] Univ Texas, Hlth Sci Ctr, Dept Pharmacol, San Antonio, TX 78229 USA
来源:
JOURNAL OF PHYSIOLOGY-LONDON
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2007年
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583卷
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01期
关键词:
D O I:
10.1113/jphysiol.2007.133231
中图分类号:
Q189 [神经科学];
学科分类号:
071006 ;
摘要:
The pharmacological desensitization of receptors is a fundamental mechanism for regulating the activity of neuronal systems. The TRPA1 channel plays a key role in the processing of noxious information and can undergo functional desensitization by unknown mechanisms. Here we show that TRPA1 is desensitized by homologous (mustard oil; a TRPA1 agonist) and heterologous (capsaicin; a TRPV1 agonist) agonists via Ca2+ -independent and Ca2+-dependent pathways, respectively, in sensory neurons. The pharmacological desensitization of TRPA1 by capsaicin and mustard oil is not influenced by activation of protein phosphatase 2B. However, it is regulated by phosphatidylinositol-4,5-bisphosphate depletion after capsaicin, but not mustard oil, application. Using a biosensor, we establish that capsaicin, unlike mustard oil, consistently activates phospholipase C in sensory neurons. We next demonstrate that TRPA1 desensitization is regulated by TRPV1, and it appears that mustard oil-induced TRPA1 internalization is prevented by coexpression with TRPV1 in a heterologous expression system and in sensory neurons. In conclusion, we propose novel mechanisms whereby TRPA1 activity undergoes pharmacological desensitization through multiple cellular pathways that are agonist dependent and modulated by TRPV1.