Dorsal horn-enriched genes identified by DNA microarray, in situ hybridization and immunohistochemistry

<p>Abstract</p> <p>Background</p> <p>Neurons in the dorsal spinal cord play important roles in nociception and pain. These neurons receive input from peripheral sensory neurons and then transmit the signals to the brain, as well as receive and integrate descending contr...

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Main Authors: Koblan Kenneth S, Holder Daniel J, Kinose Fumi, Benz Robert J, Della Penna Kimberly B, Xu Jian, Sun Hong, Gerhold David L, Wang Hao
Format: Article
Language:English
Published: BMC 2002-08-01
Series:BMC Neuroscience
Online Access:http://www.biomedcentral.com/1471-2202/3/11
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spelling doaj-16b466e1ea4145409fd33d1a7faaf5742020-11-25T00:23:58ZengBMCBMC Neuroscience1471-22022002-08-01311110.1186/1471-2202-3-11Dorsal horn-enriched genes identified by DNA microarray, in situ hybridization and immunohistochemistryKoblan Kenneth SHolder Daniel JKinose FumiBenz Robert JDella Penna Kimberly BXu JianSun HongGerhold David LWang Hao<p>Abstract</p> <p>Background</p> <p>Neurons in the dorsal spinal cord play important roles in nociception and pain. These neurons receive input from peripheral sensory neurons and then transmit the signals to the brain, as well as receive and integrate descending control signals from the brain. Many molecules important for pain transmission have been demonstrated to be localized to the dorsal horn of the spinal cord. Further understanding of the molecular interactions and signaling pathways in the dorsal horn neurons will require a better knowledge of the molecular neuroanatomy in the dorsal spinal cord.</p> <p>Results</p> <p>A large scale screening was conducted for genes with enriched expression in the dorsal spinal cord using DNA microarray and quantitative real-time PCR. In addition to genes known to be specifically expressed in the dorsal spinal cord, other neuropeptides, receptors, ion channels, and signaling molecules were also found enriched in the dorsal spinal cord. In situ hybridization and immunohistochemistry revealed the cellular expression of a subset of these genes. The regulation of a subset of the genes was also studied in the spinal nerve ligation (SNL) neuropathic pain model. In general, we found that the genes that are enriched in the dorsal spinal cord were not among those found to be up-regulated in the spinal nerve ligation model of neuropathic pain. This study also provides a level of validation of the use of DNA microarrays in conjunction with our novel analysis algorithm (SAFER) for the identification of differences in gene expression.</p> <p>Conclusion</p> <p>This study identified molecules that are enriched in the dorsal horn of the spinal cord and provided a molecular neuroanatomy in the spinal cord, which will aid in the understanding of the molecular mechanisms important in nociception and pain.</p> http://www.biomedcentral.com/1471-2202/3/11
collection DOAJ
language English
format Article
sources DOAJ
author Koblan Kenneth S
Holder Daniel J
Kinose Fumi
Benz Robert J
Della Penna Kimberly B
Xu Jian
Sun Hong
Gerhold David L
Wang Hao
spellingShingle Koblan Kenneth S
Holder Daniel J
Kinose Fumi
Benz Robert J
Della Penna Kimberly B
Xu Jian
Sun Hong
Gerhold David L
Wang Hao
Dorsal horn-enriched genes identified by DNA microarray, in situ hybridization and immunohistochemistry
BMC Neuroscience
author_facet Koblan Kenneth S
Holder Daniel J
Kinose Fumi
Benz Robert J
Della Penna Kimberly B
Xu Jian
Sun Hong
Gerhold David L
Wang Hao
author_sort Koblan Kenneth S
title Dorsal horn-enriched genes identified by DNA microarray, in situ hybridization and immunohistochemistry
title_short Dorsal horn-enriched genes identified by DNA microarray, in situ hybridization and immunohistochemistry
title_full Dorsal horn-enriched genes identified by DNA microarray, in situ hybridization and immunohistochemistry
title_fullStr Dorsal horn-enriched genes identified by DNA microarray, in situ hybridization and immunohistochemistry
title_full_unstemmed Dorsal horn-enriched genes identified by DNA microarray, in situ hybridization and immunohistochemistry
title_sort dorsal horn-enriched genes identified by dna microarray, in situ hybridization and immunohistochemistry
publisher BMC
series BMC Neuroscience
issn 1471-2202
publishDate 2002-08-01
description <p>Abstract</p> <p>Background</p> <p>Neurons in the dorsal spinal cord play important roles in nociception and pain. These neurons receive input from peripheral sensory neurons and then transmit the signals to the brain, as well as receive and integrate descending control signals from the brain. Many molecules important for pain transmission have been demonstrated to be localized to the dorsal horn of the spinal cord. Further understanding of the molecular interactions and signaling pathways in the dorsal horn neurons will require a better knowledge of the molecular neuroanatomy in the dorsal spinal cord.</p> <p>Results</p> <p>A large scale screening was conducted for genes with enriched expression in the dorsal spinal cord using DNA microarray and quantitative real-time PCR. In addition to genes known to be specifically expressed in the dorsal spinal cord, other neuropeptides, receptors, ion channels, and signaling molecules were also found enriched in the dorsal spinal cord. In situ hybridization and immunohistochemistry revealed the cellular expression of a subset of these genes. The regulation of a subset of the genes was also studied in the spinal nerve ligation (SNL) neuropathic pain model. In general, we found that the genes that are enriched in the dorsal spinal cord were not among those found to be up-regulated in the spinal nerve ligation model of neuropathic pain. This study also provides a level of validation of the use of DNA microarrays in conjunction with our novel analysis algorithm (SAFER) for the identification of differences in gene expression.</p> <p>Conclusion</p> <p>This study identified molecules that are enriched in the dorsal horn of the spinal cord and provided a molecular neuroanatomy in the spinal cord, which will aid in the understanding of the molecular mechanisms important in nociception and pain.</p>
url http://www.biomedcentral.com/1471-2202/3/11
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