Loss of corneal sensory nerve fibers in SIV-infected macaques: an alternate approach to investigate HIV-induced PNS damage
Peripheral neuropathy is the most frequent neurological complication of HIV infection, affecting more than one-third of infected patients, including patients treated with antiretroviral therapy. Although emerging noninvasive techniques for corneal nerve assessments are increasingly being used to dia...
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Veröffentlicht in: | The American journal of pathology 2014-06, Vol.184 (6), p.1652-1659 |
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creator | Dorsey, Jamie L Mangus, Lisa M Oakley, Jonathan D Beck, Sarah E Kelly, Kathleen M Queen, Suzanne E Metcalf Pate, Kelly A Adams, Robert J Marfurt, Carl F Mankowski, Joseph L |
description | Peripheral neuropathy is the most frequent neurological complication of HIV infection, affecting more than one-third of infected patients, including patients treated with antiretroviral therapy. Although emerging noninvasive techniques for corneal nerve assessments are increasingly being used to diagnose and monitor peripheral neuropathies, corneal nerve alterations have not been characterized in HIV. Here, to determine whether SIV infection leads to corneal nerve fiber loss, we immunostained corneas for the nerve fiber marker βIII tubulin. We developed and applied both manual and automated methods to measure nerves in the corneal subbasal plexus. These counting methods independently indicated significantly lower subbasal corneal nerve fiber density among SIV-infected animals that rapidly progressed to AIDS compared with slow progressors. Concomitant with decreased corneal nerve fiber density, rapid progressors had increased levels of SIV RNA and CD68-positive macrophages and expression of glial fibrillary acidic protein by glial satellite cells in the trigeminal ganglia, the location of the neuronal cell bodies of corneal sensory nerve fibers. In addition, corneal nerve fiber density was directly correlated with epidermal nerve fiber length. These findings indicate that corneal nerve assessment has great potential to diagnose and monitor HIV-induced peripheral neuropathy and to set the stage for introducing noninvasive techniques to measure corneal nerve fiber density in HIV clinical settings. |
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Although emerging noninvasive techniques for corneal nerve assessments are increasingly being used to diagnose and monitor peripheral neuropathies, corneal nerve alterations have not been characterized in HIV. Here, to determine whether SIV infection leads to corneal nerve fiber loss, we immunostained corneas for the nerve fiber marker βIII tubulin. We developed and applied both manual and automated methods to measure nerves in the corneal subbasal plexus. These counting methods independently indicated significantly lower subbasal corneal nerve fiber density among SIV-infected animals that rapidly progressed to AIDS compared with slow progressors. Concomitant with decreased corneal nerve fiber density, rapid progressors had increased levels of SIV RNA and CD68-positive macrophages and expression of glial fibrillary acidic protein by glial satellite cells in the trigeminal ganglia, the location of the neuronal cell bodies of corneal sensory nerve fibers. In addition, corneal nerve fiber density was directly correlated with epidermal nerve fiber length. These findings indicate that corneal nerve assessment has great potential to diagnose and monitor HIV-induced peripheral neuropathy and to set the stage for introducing noninvasive techniques to measure corneal nerve fiber density in HIV clinical settings.</description><identifier>ISSN: 0002-9440</identifier><identifier>EISSN: 1525-2191</identifier><identifier>DOI: 10.1016/j.ajpath.2014.02.009</identifier><identifier>PMID: 24828391</identifier><language>eng</language><publisher>United States: American Society for Investigative Pathology</publisher><subject>Animals ; Cornea - innervation ; Cornea - pathology ; Cornea - secretion ; Epidermis - innervation ; Epidermis - metabolism ; Epidermis - pathology ; Glial Fibrillary Acidic Protein - metabolism ; HIV Infections - metabolism ; HIV Infections - prevention & control ; HIV-1 ; Macaca nemestrina ; Nerve Fibers - metabolism ; Nerve Fibers - pathology ; Peripheral Nervous System Diseases - metabolism ; Peripheral Nervous System Diseases - pathology ; Short Communication ; Simian Acquired Immunodeficiency Syndrome - metabolism ; Simian Acquired Immunodeficiency Syndrome - pathology ; Simian Immunodeficiency Virus</subject><ispartof>The American journal of pathology, 2014-06, Vol.184 (6), p.1652-1659</ispartof><rights>Copyright © 2014 American Society for Investigative Pathology. Published by Elsevier Inc. All rights reserved.</rights><rights>2014 American Society for Investigative Pathology. Published by Elsevier Inc. All rights reserved. 2014 American Society for Investigative Pathology</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC4044714/pdf/$$EPDF$$P50$$Gpubmedcentral$$H</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC4044714/$$EHTML$$P50$$Gpubmedcentral$$H</linktohtml><link.rule.ids>230,314,727,780,784,885,27924,27925,53791,53793</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/24828391$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Dorsey, Jamie L</creatorcontrib><creatorcontrib>Mangus, Lisa M</creatorcontrib><creatorcontrib>Oakley, Jonathan D</creatorcontrib><creatorcontrib>Beck, Sarah E</creatorcontrib><creatorcontrib>Kelly, Kathleen M</creatorcontrib><creatorcontrib>Queen, Suzanne E</creatorcontrib><creatorcontrib>Metcalf Pate, Kelly A</creatorcontrib><creatorcontrib>Adams, Robert J</creatorcontrib><creatorcontrib>Marfurt, Carl F</creatorcontrib><creatorcontrib>Mankowski, Joseph L</creatorcontrib><title>Loss of corneal sensory nerve fibers in SIV-infected macaques: an alternate approach to investigate HIV-induced PNS damage</title><title>The American journal of pathology</title><addtitle>Am J Pathol</addtitle><description>Peripheral neuropathy is the most frequent neurological complication of HIV infection, affecting more than one-third of infected patients, including patients treated with antiretroviral therapy. Although emerging noninvasive techniques for corneal nerve assessments are increasingly being used to diagnose and monitor peripheral neuropathies, corneal nerve alterations have not been characterized in HIV. Here, to determine whether SIV infection leads to corneal nerve fiber loss, we immunostained corneas for the nerve fiber marker βIII tubulin. We developed and applied both manual and automated methods to measure nerves in the corneal subbasal plexus. These counting methods independently indicated significantly lower subbasal corneal nerve fiber density among SIV-infected animals that rapidly progressed to AIDS compared with slow progressors. Concomitant with decreased corneal nerve fiber density, rapid progressors had increased levels of SIV RNA and CD68-positive macrophages and expression of glial fibrillary acidic protein by glial satellite cells in the trigeminal ganglia, the location of the neuronal cell bodies of corneal sensory nerve fibers. In addition, corneal nerve fiber density was directly correlated with epidermal nerve fiber length. These findings indicate that corneal nerve assessment has great potential to diagnose and monitor HIV-induced peripheral neuropathy and to set the stage for introducing noninvasive techniques to measure corneal nerve fiber density in HIV clinical settings.</description><subject>Animals</subject><subject>Cornea - innervation</subject><subject>Cornea - pathology</subject><subject>Cornea - secretion</subject><subject>Epidermis - innervation</subject><subject>Epidermis - metabolism</subject><subject>Epidermis - pathology</subject><subject>Glial Fibrillary Acidic Protein - metabolism</subject><subject>HIV Infections - metabolism</subject><subject>HIV Infections - prevention & control</subject><subject>HIV-1</subject><subject>Macaca nemestrina</subject><subject>Nerve Fibers - metabolism</subject><subject>Nerve Fibers - pathology</subject><subject>Peripheral Nervous System Diseases - metabolism</subject><subject>Peripheral Nervous System Diseases - pathology</subject><subject>Short Communication</subject><subject>Simian Acquired Immunodeficiency Syndrome - metabolism</subject><subject>Simian Acquired Immunodeficiency Syndrome - pathology</subject><subject>Simian Immunodeficiency Virus</subject><issn>0002-9440</issn><issn>1525-2191</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2014</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNpVUEtr3DAQFiWl2aT9ByXomIud0WMduYdCCEk3sDSBbXs1Y3m868WWHEm7kP76Ok_S0zCP7zEfY18F5AJEcbbNcTti2uQShM5B5gDlBzYTcznPpCjFAZsBgMxKreGQHcW4ndpCGfjEDqU20qhSzNjfpY-R-5ZbHxxhzyO56MMDdxT2xNuuphB55_jq5k_WuZZsooYPaPF-R_EbR8exTxQcJuI4jsGj3fDkJ8ieYurWj_PFE7bZ2Ql693PFGxxwTZ_Zxxb7SF9e6jH7fX3163KRLW9_3FxeLLNRFkXKRKGs0UZpkmDn1gqtpcVWtsKWUBdG6FYKhFbV2uimaEDh5BJrsLLWoqzVMfv-zDvu6oEaSy4F7KsxdAOGh8pjV_2_cd2mWvt9pUHrc6EngtMXguAfv07V0EVLfY-O_C5WU-RGqXMzl9PpyXutN5HXwNU_ub-G2A</recordid><startdate>20140601</startdate><enddate>20140601</enddate><creator>Dorsey, Jamie L</creator><creator>Mangus, Lisa M</creator><creator>Oakley, Jonathan D</creator><creator>Beck, Sarah E</creator><creator>Kelly, Kathleen M</creator><creator>Queen, Suzanne E</creator><creator>Metcalf Pate, Kelly A</creator><creator>Adams, Robert J</creator><creator>Marfurt, Carl F</creator><creator>Mankowski, Joseph L</creator><general>American Society for Investigative Pathology</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>7X8</scope><scope>5PM</scope></search><sort><creationdate>20140601</creationdate><title>Loss of corneal sensory nerve fibers in SIV-infected macaques: an alternate approach to investigate HIV-induced PNS damage</title><author>Dorsey, Jamie L ; Mangus, Lisa M ; Oakley, Jonathan D ; Beck, Sarah E ; Kelly, Kathleen M ; Queen, Suzanne E ; Metcalf Pate, Kelly A ; Adams, Robert J ; Marfurt, Carl F ; Mankowski, Joseph L</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-p266t-163c84834e20c5cc1442caf2f1c90b6814f21a0f3b484d6d03afecab0c2b419b3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2014</creationdate><topic>Animals</topic><topic>Cornea - innervation</topic><topic>Cornea - pathology</topic><topic>Cornea - secretion</topic><topic>Epidermis - innervation</topic><topic>Epidermis - metabolism</topic><topic>Epidermis - pathology</topic><topic>Glial Fibrillary Acidic Protein - metabolism</topic><topic>HIV Infections - metabolism</topic><topic>HIV Infections - prevention & control</topic><topic>HIV-1</topic><topic>Macaca nemestrina</topic><topic>Nerve Fibers - metabolism</topic><topic>Nerve Fibers - pathology</topic><topic>Peripheral Nervous System Diseases - metabolism</topic><topic>Peripheral Nervous System Diseases - pathology</topic><topic>Short Communication</topic><topic>Simian Acquired Immunodeficiency Syndrome - metabolism</topic><topic>Simian Acquired Immunodeficiency Syndrome - pathology</topic><topic>Simian Immunodeficiency Virus</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Dorsey, Jamie L</creatorcontrib><creatorcontrib>Mangus, Lisa M</creatorcontrib><creatorcontrib>Oakley, Jonathan D</creatorcontrib><creatorcontrib>Beck, Sarah E</creatorcontrib><creatorcontrib>Kelly, Kathleen M</creatorcontrib><creatorcontrib>Queen, Suzanne E</creatorcontrib><creatorcontrib>Metcalf Pate, Kelly A</creatorcontrib><creatorcontrib>Adams, Robert J</creatorcontrib><creatorcontrib>Marfurt, Carl F</creatorcontrib><creatorcontrib>Mankowski, Joseph L</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>The American journal of pathology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Dorsey, Jamie L</au><au>Mangus, Lisa M</au><au>Oakley, Jonathan D</au><au>Beck, Sarah E</au><au>Kelly, Kathleen M</au><au>Queen, Suzanne E</au><au>Metcalf Pate, Kelly A</au><au>Adams, Robert J</au><au>Marfurt, Carl F</au><au>Mankowski, Joseph L</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Loss of corneal sensory nerve fibers in SIV-infected macaques: an alternate approach to investigate HIV-induced PNS damage</atitle><jtitle>The American journal of pathology</jtitle><addtitle>Am J Pathol</addtitle><date>2014-06-01</date><risdate>2014</risdate><volume>184</volume><issue>6</issue><spage>1652</spage><epage>1659</epage><pages>1652-1659</pages><issn>0002-9440</issn><eissn>1525-2191</eissn><abstract>Peripheral neuropathy is the most frequent neurological complication of HIV infection, affecting more than one-third of infected patients, including patients treated with antiretroviral therapy. Although emerging noninvasive techniques for corneal nerve assessments are increasingly being used to diagnose and monitor peripheral neuropathies, corneal nerve alterations have not been characterized in HIV. Here, to determine whether SIV infection leads to corneal nerve fiber loss, we immunostained corneas for the nerve fiber marker βIII tubulin. We developed and applied both manual and automated methods to measure nerves in the corneal subbasal plexus. These counting methods independently indicated significantly lower subbasal corneal nerve fiber density among SIV-infected animals that rapidly progressed to AIDS compared with slow progressors. Concomitant with decreased corneal nerve fiber density, rapid progressors had increased levels of SIV RNA and CD68-positive macrophages and expression of glial fibrillary acidic protein by glial satellite cells in the trigeminal ganglia, the location of the neuronal cell bodies of corneal sensory nerve fibers. 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subjects | Animals Cornea - innervation Cornea - pathology Cornea - secretion Epidermis - innervation Epidermis - metabolism Epidermis - pathology Glial Fibrillary Acidic Protein - metabolism HIV Infections - metabolism HIV Infections - prevention & control HIV-1 Macaca nemestrina Nerve Fibers - metabolism Nerve Fibers - pathology Peripheral Nervous System Diseases - metabolism Peripheral Nervous System Diseases - pathology Short Communication Simian Acquired Immunodeficiency Syndrome - metabolism Simian Acquired Immunodeficiency Syndrome - pathology Simian Immunodeficiency Virus |
title | Loss of corneal sensory nerve fibers in SIV-infected macaques: an alternate approach to investigate HIV-induced PNS damage |
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