Preserved acute pain and impaired neuropathic pain in mice lacking protein interacting with C Kinase 1

被引:33
|
作者
Wang, Wei [1 ,2 ]
Petralia, Ronald S. [3 ]
Takamiya, Kogo [4 ]
Xia, Jun [4 ,5 ]
Li, Yun-Qing [1 ,2 ]
Huganir, Richard L. [4 ]
Tao, Yuan-Xiang [1 ]
Yaster, Myron [1 ]
机构
[1] Johns Hopkins Univ, Sch Med, Dept Anesthesiol & Crit Care Med, Baltimore, MD 21205 USA
[2] Fourth Mil Med Univ, Dept Anat Histol & Embryol, KK Leung Brain Res Ctr, Xian 710032, Peoples R China
[3] Natl Inst Deafness & Other Commun Disorders, Neurochem Lab, NIH, Bethesda, MD 20892 USA
[4] Johns Hopkins Univ, Sch Med, Dept Neurosci, Baltimore, MD 21287 USA
[5] Hong Kong Univ Sci & Technol, Dept Biochem, Kowloon, Hong Kong, Peoples R China
来源
MOLECULAR PAIN | 2011年 / 7卷
基金
美国国家卫生研究院;
关键词
METABOTROPIC GLUTAMATE RECEPTORS; PERIPHERAL-NERVE INJURY; CORD DORSAL-HORN; SPINAL-CORD; PDZ DOMAIN; PERSISTENT PAIN; EXCITATORY SYNAPSES; INFLAMMATORY PAIN; GANGLION NEURONS; PICK1; INTERACTS;
D O I
10.1186/1744-8069-7-11
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Protein interacting with C Kinase 1 (PICK1), a PDZ domain-containing scaffolding protein, interacts with multiple different proteins in the mammalian nervous system and is believed to play important roles in diverse physiological and pathological conditions. In this study, we report that PICK1 is expressed in neurons of the dorsal root ganglion (DRG) and spinal cord dorsal horn, two major pain-related regions. PICK1 was present in approximately 29.7% of DRG neurons, most of which were small-less than 750 mu m(2) in cross-sectional area. Some of these PICK1-positive cells co-labeled with isolectin B4 or calcitonin-gene-related peptide. In the dorsal horn, PICK1 immunoreactivity was concentrated in the superficial dorsal horn, where it was prominent in the postsynaptic density, axons, and dendrites. Targeted disruption of PICK1 gene did not affect basal paw withdrawal responses to acute noxious thermal and mechanical stimuli or locomotor reflex activity, but it completely blocked the induction of peripheral nerve injury-induced mechanical and thermal pain hypersensitivities. PICK1 appears to be required for peripheral nerve injury-induced neuropathic pain development and to be a potential biochemical target for treating this disorder.
引用
收藏
页数:11
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