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Vgf is a novel biomarker associated with muscle weakness in amyotrophic lateral sclerosis (ALS), with a potential role in disease pathogenesis
Amyotrophic lateral sclerosis (ALS) is a progressive neurodegenerative disease that affects nerve cells in the brain and the spinal cord. Previous proteomic evidence revealed that the content of certain peptide fragments including Vgf-derived peptide aa 398-411 (Vgf(398-411)) of the precursor Vgf pr...
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Published in: | International journal of medical sciences 2008-04, Vol.5 (2), p.92-99 |
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description | Amyotrophic lateral sclerosis (ALS) is a progressive neurodegenerative disease that affects nerve cells in the brain and the spinal cord. Previous proteomic evidence revealed that the content of certain peptide fragments including Vgf-derived peptide aa 398-411 (Vgf(398-411)) of the precursor Vgf protein in the cerebral spinal fluid (CSF) correctly identified patients with ALS from normal and disease controls. Using quantitative ELISA immunoassay we found that the CSF levels of Vgf decreases with muscle weakness in patients with ALS. In SOD1 G93A transgenic mice, loss of full-length Vgf content in CSF, serum and in SMI-32 immunopositive spinal cord motor neurons is noted in asymptomatic animals (approximately 75 days old) and continues to show a progressive decline as animals weaken. In vitro studies show that viral-mediated exogenous Vgf expression in primary mixed spinal cord neuron cultures attenuates excitotoxic injury. Thus, while Vgf may be a reliable biomarker of progression of muscle weakness in patients with ALS, restoration of Vgf expression in spinal cord motor neurons may therapeutically rescue spinal cord motorneurons against excitotoxic injury. |
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Previous proteomic evidence revealed that the content of certain peptide fragments including Vgf-derived peptide aa 398-411 (Vgf(398-411)) of the precursor Vgf protein in the cerebral spinal fluid (CSF) correctly identified patients with ALS from normal and disease controls. Using quantitative ELISA immunoassay we found that the CSF levels of Vgf decreases with muscle weakness in patients with ALS. In SOD1 G93A transgenic mice, loss of full-length Vgf content in CSF, serum and in SMI-32 immunopositive spinal cord motor neurons is noted in asymptomatic animals (approximately 75 days old) and continues to show a progressive decline as animals weaken. In vitro studies show that viral-mediated exogenous Vgf expression in primary mixed spinal cord neuron cultures attenuates excitotoxic injury. Thus, while Vgf may be a reliable biomarker of progression of muscle weakness in patients with ALS, restoration of Vgf expression in spinal cord motor neurons may therapeutically rescue spinal cord motorneurons against excitotoxic injury.</description><identifier>ISSN: 1449-1907</identifier><identifier>EISSN: 1449-1907</identifier><identifier>DOI: 10.7150/ijms.5.92</identifier><identifier>PMID: 18432310</identifier><language>eng</language><publisher>Australia: Ivyspring International Publisher</publisher><subject>Amyotrophic Lateral Sclerosis - metabolism ; Amyotrophic Lateral Sclerosis - pathology ; Amyotrophic Lateral Sclerosis - physiopathology ; Animals ; Biomarkers - metabolism ; Enzyme-Linked Immunosorbent Assay ; Humans ; Immunohistochemistry ; Mice ; Mice, Transgenic ; Muscle Weakness ; Nerve Growth Factors - blood ; Nerve Growth Factors - cerebrospinal fluid ; Nerve Growth Factors - metabolism ; Neuropeptides - blood ; Neuropeptides - cerebrospinal fluid ; Neuropeptides - metabolism ; Research Paper ; Sensitivity and Specificity ; Severity of Illness Index ; Superoxide Dismutase - genetics</subject><ispartof>International journal of medical sciences, 2008-04, Vol.5 (2), p.92-99</ispartof><rights>Ivyspring International Publisher. This is an open-access article distributed under the terms of the Creative Commons License (http://creativecommons.org/licenses/by-nc-nd/3.0/). Reproduction is permitted for personal, noncommercial use, provided that the article is in whole, unmodified, and properly cited. 2008</rights><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c3542-5156ab2bcafd8809ffdb926eb8295364e4640205be01fe6decb6cb659f6596263</citedby></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC2323610/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC2323610/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,314,727,780,784,885,27924,27925,53791,53793</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/18432310$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Zhao, Zhong</creatorcontrib><creatorcontrib>Lange, Dale J</creatorcontrib><creatorcontrib>Ho, Lap</creatorcontrib><creatorcontrib>Bonini, Sara</creatorcontrib><creatorcontrib>Shao, Belinda</creatorcontrib><creatorcontrib>Salton, Stephen R</creatorcontrib><creatorcontrib>Thomas, Sunil</creatorcontrib><creatorcontrib>Pasinetti, Giulio Maria</creatorcontrib><title>Vgf is a novel biomarker associated with muscle weakness in amyotrophic lateral sclerosis (ALS), with a potential role in disease pathogenesis</title><title>International journal of medical sciences</title><addtitle>Int J Med Sci</addtitle><description>Amyotrophic lateral sclerosis (ALS) is a progressive neurodegenerative disease that affects nerve cells in the brain and the spinal cord. Previous proteomic evidence revealed that the content of certain peptide fragments including Vgf-derived peptide aa 398-411 (Vgf(398-411)) of the precursor Vgf protein in the cerebral spinal fluid (CSF) correctly identified patients with ALS from normal and disease controls. Using quantitative ELISA immunoassay we found that the CSF levels of Vgf decreases with muscle weakness in patients with ALS. In SOD1 G93A transgenic mice, loss of full-length Vgf content in CSF, serum and in SMI-32 immunopositive spinal cord motor neurons is noted in asymptomatic animals (approximately 75 days old) and continues to show a progressive decline as animals weaken. In vitro studies show that viral-mediated exogenous Vgf expression in primary mixed spinal cord neuron cultures attenuates excitotoxic injury. Thus, while Vgf may be a reliable biomarker of progression of muscle weakness in patients with ALS, restoration of Vgf expression in spinal cord motor neurons may therapeutically rescue spinal cord motorneurons against excitotoxic injury.</description><subject>Amyotrophic Lateral Sclerosis - metabolism</subject><subject>Amyotrophic Lateral Sclerosis - pathology</subject><subject>Amyotrophic Lateral Sclerosis - physiopathology</subject><subject>Animals</subject><subject>Biomarkers - metabolism</subject><subject>Enzyme-Linked Immunosorbent Assay</subject><subject>Humans</subject><subject>Immunohistochemistry</subject><subject>Mice</subject><subject>Mice, Transgenic</subject><subject>Muscle Weakness</subject><subject>Nerve Growth Factors - blood</subject><subject>Nerve Growth Factors - cerebrospinal fluid</subject><subject>Nerve Growth Factors - metabolism</subject><subject>Neuropeptides - blood</subject><subject>Neuropeptides - cerebrospinal fluid</subject><subject>Neuropeptides - metabolism</subject><subject>Research Paper</subject><subject>Sensitivity and Specificity</subject><subject>Severity of Illness Index</subject><subject>Superoxide Dismutase - genetics</subject><issn>1449-1907</issn><issn>1449-1907</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2008</creationdate><recordtype>article</recordtype><sourceid>DOA</sourceid><recordid>eNpVkttu1DAQhiMEoqVwwQsgXyEqsYvHsb3xTaWq4lBpJS443FoTZ7LrbRIHO9uqL8Ez47AraCVbHtn_fJ5TUbwGvlyB4h_8rk9LtTTiSXEKUpoFGL56-sA-KV6ktOO8FOUKnhcnUMlsAj8tfv_ctMwnhmwIt9Sx2oce4w1FhikF53Giht35acv6fXIdsTvCm4FSYn5g2N-HKYZx6x3rsjJix2ZRDCkj312uv52_PzgjG8NEw-SzIoaMyd6NT4SJ2IjTNmwoQ316WTxrsUv06nieFT8-ffx-9WWx_vr5-upyvXClkmKhQGmsRe2wbaqKm7ZtaiM01ZUwqtSSpJZccFUTh5Z0Q67WeSnT5q2FLs-K6wO3CbizY_Q56Xsb0Nu_FyFuLMbJ51xsVTfGgQTKfInAkasGdCs1OLFCKTLr4sAa93VPjctp5kI8gj5-GfzWbsKtFbkHGngGvD0CYvi1pzTZ3idHXYcDhX2y2kAJwOeozw9ClyucIrX_PgFu50mw8yRYZc0c1ZuHUf1XHltf_gEL6rIn</recordid><startdate>20080415</startdate><enddate>20080415</enddate><creator>Zhao, Zhong</creator><creator>Lange, Dale J</creator><creator>Ho, Lap</creator><creator>Bonini, Sara</creator><creator>Shao, Belinda</creator><creator>Salton, Stephen R</creator><creator>Thomas, Sunil</creator><creator>Pasinetti, Giulio Maria</creator><general>Ivyspring International Publisher</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope><scope>5PM</scope><scope>DOA</scope></search><sort><creationdate>20080415</creationdate><title>Vgf is a novel biomarker associated with muscle weakness in amyotrophic lateral sclerosis (ALS), with a potential role in disease pathogenesis</title><author>Zhao, Zhong ; Lange, Dale J ; Ho, Lap ; Bonini, Sara ; Shao, Belinda ; Salton, Stephen R ; Thomas, Sunil ; Pasinetti, Giulio Maria</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c3542-5156ab2bcafd8809ffdb926eb8295364e4640205be01fe6decb6cb659f6596263</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2008</creationdate><topic>Amyotrophic Lateral Sclerosis - metabolism</topic><topic>Amyotrophic Lateral Sclerosis - pathology</topic><topic>Amyotrophic Lateral Sclerosis - physiopathology</topic><topic>Animals</topic><topic>Biomarkers - metabolism</topic><topic>Enzyme-Linked Immunosorbent Assay</topic><topic>Humans</topic><topic>Immunohistochemistry</topic><topic>Mice</topic><topic>Mice, Transgenic</topic><topic>Muscle Weakness</topic><topic>Nerve Growth Factors - blood</topic><topic>Nerve Growth Factors - cerebrospinal fluid</topic><topic>Nerve Growth Factors - metabolism</topic><topic>Neuropeptides - blood</topic><topic>Neuropeptides - cerebrospinal fluid</topic><topic>Neuropeptides - metabolism</topic><topic>Research Paper</topic><topic>Sensitivity and Specificity</topic><topic>Severity of Illness Index</topic><topic>Superoxide Dismutase - genetics</topic><toplevel>online_resources</toplevel><creatorcontrib>Zhao, Zhong</creatorcontrib><creatorcontrib>Lange, Dale J</creatorcontrib><creatorcontrib>Ho, Lap</creatorcontrib><creatorcontrib>Bonini, Sara</creatorcontrib><creatorcontrib>Shao, Belinda</creatorcontrib><creatorcontrib>Salton, Stephen R</creatorcontrib><creatorcontrib>Thomas, Sunil</creatorcontrib><creatorcontrib>Pasinetti, Giulio Maria</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><collection>DOAJ Directory of Open Access Journals</collection><jtitle>International journal of medical sciences</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Zhao, Zhong</au><au>Lange, Dale J</au><au>Ho, Lap</au><au>Bonini, Sara</au><au>Shao, Belinda</au><au>Salton, Stephen R</au><au>Thomas, Sunil</au><au>Pasinetti, Giulio Maria</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Vgf is a novel biomarker associated with muscle weakness in amyotrophic lateral sclerosis (ALS), with a potential role in disease pathogenesis</atitle><jtitle>International journal of medical sciences</jtitle><addtitle>Int J Med Sci</addtitle><date>2008-04-15</date><risdate>2008</risdate><volume>5</volume><issue>2</issue><spage>92</spage><epage>99</epage><pages>92-99</pages><issn>1449-1907</issn><eissn>1449-1907</eissn><abstract>Amyotrophic lateral sclerosis (ALS) is a progressive neurodegenerative disease that affects nerve cells in the brain and the spinal cord. Previous proteomic evidence revealed that the content of certain peptide fragments including Vgf-derived peptide aa 398-411 (Vgf(398-411)) of the precursor Vgf protein in the cerebral spinal fluid (CSF) correctly identified patients with ALS from normal and disease controls. Using quantitative ELISA immunoassay we found that the CSF levels of Vgf decreases with muscle weakness in patients with ALS. In SOD1 G93A transgenic mice, loss of full-length Vgf content in CSF, serum and in SMI-32 immunopositive spinal cord motor neurons is noted in asymptomatic animals (approximately 75 days old) and continues to show a progressive decline as animals weaken. In vitro studies show that viral-mediated exogenous Vgf expression in primary mixed spinal cord neuron cultures attenuates excitotoxic injury. 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subjects | Amyotrophic Lateral Sclerosis - metabolism Amyotrophic Lateral Sclerosis - pathology Amyotrophic Lateral Sclerosis - physiopathology Animals Biomarkers - metabolism Enzyme-Linked Immunosorbent Assay Humans Immunohistochemistry Mice Mice, Transgenic Muscle Weakness Nerve Growth Factors - blood Nerve Growth Factors - cerebrospinal fluid Nerve Growth Factors - metabolism Neuropeptides - blood Neuropeptides - cerebrospinal fluid Neuropeptides - metabolism Research Paper Sensitivity and Specificity Severity of Illness Index Superoxide Dismutase - genetics |
title | Vgf is a novel biomarker associated with muscle weakness in amyotrophic lateral sclerosis (ALS), with a potential role in disease pathogenesis |
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