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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...
Autores principales: | , , , , , , , |
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Formato: | Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2011
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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. |
format | Text |
id | pubmed-3038962 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2011 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
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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