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

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 ex...

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Autores principales: Wang, Wei, Petralia, Ronald S, Takamiya, Kogo, Xia, Jun, Li, Yun-Qing, Huganir, Richard L, Tao, Yuan-Xiang, Yaster, Myron
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3038962/
https://www.ncbi.nlm.nih.gov/pubmed/21291534
http://dx.doi.org/10.1186/1744-8069-7-11
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author Wang, Wei
Petralia, Ronald S
Takamiya, Kogo
Xia, Jun
Li, Yun-Qing
Huganir, Richard L
Tao, Yuan-Xiang
Yaster, Myron
author_facet Wang, Wei
Petralia, Ronald S
Takamiya, Kogo
Xia, Jun
Li, Yun-Qing
Huganir, Richard L
Tao, Yuan-Xiang
Yaster, Myron
author_sort Wang, Wei
collection PubMed
description 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 μm(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.
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spelling pubmed-30389622011-02-15 Preserved acute pain and impaired neuropathic pain in mice lacking protein interacting with C Kinase 1 Wang, Wei Petralia, Ronald S Takamiya, Kogo Xia, Jun Li, Yun-Qing Huganir, Richard L Tao, Yuan-Xiang Yaster, Myron Mol Pain Research 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 μm(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. BioMed Central 2011-02-03 /pmc/articles/PMC3038962/ /pubmed/21291534 http://dx.doi.org/10.1186/1744-8069-7-11 Text en Copyright ©2011 Wang et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research
Wang, Wei
Petralia, Ronald S
Takamiya, Kogo
Xia, Jun
Li, Yun-Qing
Huganir, Richard L
Tao, Yuan-Xiang
Yaster, Myron
Preserved acute pain and impaired neuropathic pain in mice lacking protein interacting with C Kinase 1
title Preserved acute pain and impaired neuropathic pain in mice lacking protein interacting with C Kinase 1
title_full Preserved acute pain and impaired neuropathic pain in mice lacking protein interacting with C Kinase 1
title_fullStr Preserved acute pain and impaired neuropathic pain in mice lacking protein interacting with C Kinase 1
title_full_unstemmed Preserved acute pain and impaired neuropathic pain in mice lacking protein interacting with C Kinase 1
title_short Preserved acute pain and impaired neuropathic pain in mice lacking protein interacting with C Kinase 1
title_sort preserved acute pain and impaired neuropathic pain in mice lacking protein interacting with c kinase 1
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3038962/
https://www.ncbi.nlm.nih.gov/pubmed/21291534
http://dx.doi.org/10.1186/1744-8069-7-11
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