Heparanase Overexpresses in Keratoconic Cornea and Tears Depending on the Pathologic Grade
Background. Keratoconus has classically been defined as a noninflammatory disorder, although recent studies show elevated levels of inflammatory markers suggesting that keratoconus could be, at least in part, an inflammatory condition. Heparanase upregulation has been described in multiple inflammat...
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creator | Quirós, Luis M. Vazquez, Fernando Lisa, Carlos González, Javier Alcalde, Ignacio Ferrara, Guilherme Merayo-Lloves, Jesús García-Suárez, Olivia García, Beatriz Alfonso, Jose F. |
description | Background. Keratoconus has classically been defined as a noninflammatory disorder, although recent studies show elevated levels of inflammatory markers suggesting that keratoconus could be, at least in part, an inflammatory condition. Heparanase upregulation has been described in multiple inflammatory disorders. In this article, we study the differential expression of heparanase in cornea and tears from keratoconus patients and healthy controls. Methods. A transcriptomic approach was used employing quantitative polymerase chain reaction to analyze the expression of heparanase and heparanase 2 in stromal and epithelial corneal cells. The protein expression was analyzed by immunohistochemistry in corneal sections. Enzymatic activity in tears was measured using [3H]-labeled heparan sulfate as substrate. Results. Heparanase transcription was detected in stromal and epithelial cells and appeared upregulated in keratoconus. Overexpression of the enzyme was also detected by immunohistochemistry. Corneal expression of heparanase 2 was detected in some cases. Heparanase catalytic activity was found in tears and displayed a positive correlation with the degree of keratoconus. Conclusions. Heparanase overexpresses in keratoconic corneas, possibly reinforcing the inflammatory condition of the pathology. The presence of heparanase activity in tears allows us to propose its use as a biomarker for the diagnosis of the disorder. |
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Keratoconus has classically been defined as a noninflammatory disorder, although recent studies show elevated levels of inflammatory markers suggesting that keratoconus could be, at least in part, an inflammatory condition. Heparanase upregulation has been described in multiple inflammatory disorders. In this article, we study the differential expression of heparanase in cornea and tears from keratoconus patients and healthy controls. Methods. A transcriptomic approach was used employing quantitative polymerase chain reaction to analyze the expression of heparanase and heparanase 2 in stromal and epithelial corneal cells. The protein expression was analyzed by immunohistochemistry in corneal sections. Enzymatic activity in tears was measured using [3H]-labeled heparan sulfate as substrate. Results. Heparanase transcription was detected in stromal and epithelial cells and appeared upregulated in keratoconus. Overexpression of the enzyme was also detected by immunohistochemistry. Corneal expression of heparanase 2 was detected in some cases. Heparanase catalytic activity was found in tears and displayed a positive correlation with the degree of keratoconus. Conclusions. Heparanase overexpresses in keratoconic corneas, possibly reinforcing the inflammatory condition of the pathology. The presence of heparanase activity in tears allows us to propose its use as a biomarker for the diagnosis of the disorder.</description><identifier>ISSN: 0278-0240</identifier><identifier>EISSN: 1875-8630</identifier><identifier>DOI: 10.1155/2017/3502386</identifier><identifier>PMID: 29379222</identifier><language>eng</language><publisher>Cairo, Egypt: Hindawi Publishing Corporation</publisher><subject>Biological markers ; Biomarkers ; Biomarkers - metabolism ; Catalysis ; Catalytic activity ; Cells, Cultured ; Control methods ; Cornea ; Cornea - enzymology ; Cornea - metabolism ; Enzymatic activity ; Epithelial cells ; Gene expression ; Genetic aspects ; Glucuronidase - genetics ; Glucuronidase - metabolism ; Heparan sulfate ; Heparitin Sulfate - metabolism ; Humans ; Immunohistochemistry ; Inflammatory diseases ; Keratoconus ; Keratoconus - enzymology ; Keratoconus - metabolism ; Keratoconus - pathology ; Polymerase chain reaction ; Substrates ; Sulfates ; Tears ; Tears - enzymology ; Tears - metabolism ; Transcription ; Up-Regulation</subject><ispartof>Disease markers, 2017-01, Vol.2017 (2017), p.1-7</ispartof><rights>Copyright © 2017 Beatriz García et al.</rights><rights>COPYRIGHT 2017 John Wiley & Sons, Inc.</rights><rights>Copyright © 2017 Beatriz García et al.; This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.</rights><rights>Copyright © 2017 Beatriz García et al. 2017</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c525t-d3ecb1747be0b860d9cc138228d69e16332335ca850e4ef289e177cae3c93e123</citedby><cites>FETCH-LOGICAL-c525t-d3ecb1747be0b860d9cc138228d69e16332335ca850e4ef289e177cae3c93e123</cites><orcidid>0000-0002-0373-8209 ; 0000-0003-3505-3762</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC5742882/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC5742882/$$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/29379222$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><contributor>Theocharis, Stamatios E.</contributor><contributor>Stamatios E Theocharis</contributor><creatorcontrib>Quirós, Luis M.</creatorcontrib><creatorcontrib>Vazquez, Fernando</creatorcontrib><creatorcontrib>Lisa, Carlos</creatorcontrib><creatorcontrib>González, Javier</creatorcontrib><creatorcontrib>Alcalde, Ignacio</creatorcontrib><creatorcontrib>Ferrara, Guilherme</creatorcontrib><creatorcontrib>Merayo-Lloves, Jesús</creatorcontrib><creatorcontrib>García-Suárez, Olivia</creatorcontrib><creatorcontrib>García, Beatriz</creatorcontrib><creatorcontrib>Alfonso, Jose F.</creatorcontrib><title>Heparanase Overexpresses in Keratoconic Cornea and Tears Depending on the Pathologic Grade</title><title>Disease markers</title><addtitle>Dis Markers</addtitle><description>Background. Keratoconus has classically been defined as a noninflammatory disorder, although recent studies show elevated levels of inflammatory markers suggesting that keratoconus could be, at least in part, an inflammatory condition. Heparanase upregulation has been described in multiple inflammatory disorders. In this article, we study the differential expression of heparanase in cornea and tears from keratoconus patients and healthy controls. Methods. A transcriptomic approach was used employing quantitative polymerase chain reaction to analyze the expression of heparanase and heparanase 2 in stromal and epithelial corneal cells. The protein expression was analyzed by immunohistochemistry in corneal sections. Enzymatic activity in tears was measured using [3H]-labeled heparan sulfate as substrate. Results. Heparanase transcription was detected in stromal and epithelial cells and appeared upregulated in keratoconus. Overexpression of the enzyme was also detected by immunohistochemistry. Corneal expression of heparanase 2 was detected in some cases. Heparanase catalytic activity was found in tears and displayed a positive correlation with the degree of keratoconus. Conclusions. Heparanase overexpresses in keratoconic corneas, possibly reinforcing the inflammatory condition of the pathology. The presence of heparanase activity in tears allows us to propose its use as a biomarker for the diagnosis of the disorder.</description><subject>Biological markers</subject><subject>Biomarkers</subject><subject>Biomarkers - metabolism</subject><subject>Catalysis</subject><subject>Catalytic activity</subject><subject>Cells, Cultured</subject><subject>Control methods</subject><subject>Cornea</subject><subject>Cornea - enzymology</subject><subject>Cornea - metabolism</subject><subject>Enzymatic activity</subject><subject>Epithelial cells</subject><subject>Gene expression</subject><subject>Genetic aspects</subject><subject>Glucuronidase - genetics</subject><subject>Glucuronidase - metabolism</subject><subject>Heparan sulfate</subject><subject>Heparitin Sulfate - metabolism</subject><subject>Humans</subject><subject>Immunohistochemistry</subject><subject>Inflammatory diseases</subject><subject>Keratoconus</subject><subject>Keratoconus - enzymology</subject><subject>Keratoconus - metabolism</subject><subject>Keratoconus - pathology</subject><subject>Polymerase chain reaction</subject><subject>Substrates</subject><subject>Sulfates</subject><subject>Tears</subject><subject>Tears - enzymology</subject><subject>Tears - metabolism</subject><subject>Transcription</subject><subject>Up-Regulation</subject><issn>0278-0240</issn><issn>1875-8630</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2017</creationdate><recordtype>article</recordtype><sourceid>RHX</sourceid><sourceid>EIF</sourceid><recordid>eNqNkU2LFDEQhoMo7rh68ywBL4K2m49Od3IRllF3xYX1sF68hJp09UyWnqRNelb996aZcfw4WRAKkoenUryEPOXsNedKnQnG2zOpmJC6uUcWXLeq0o1k98mCiVZXTNTshDzK-ZYxLkxtHpITYWRrhBAL8uUSR0gQICO9vsOE38eEOWOmPtCPmGCKLgbv6DKmgEAhdPQGIWX6FkcMnQ9rGgOdNkg_wbSJQ1wX-CJBh4_Jgx6GjE8O_ZR8fv_uZnlZXV1ffFieX1VOCTVVnUS34m3drpCtdMM64xyXWgjdNQZ5I6WQUjnQimGNvdDlsm0doHRGIhfylLzZe8fdaoudwzAlGOyY_BbSDxvB279fgt_Ydbyzqq2F1rPgxUGQ4tcd5slufXY4DBAw7rLlxkjGuW5UQZ__g97GXQplPVtyYLoxstSRWsOA1oc-lrlultpzpUoM5cyuV3vKpZhzwv74Zc7sHO2sbO0h2oI_-3PNI_wrywK83AMbHzr45v9Th4XBHn7TXAlhmPwJOVuz-A</recordid><startdate>20170101</startdate><enddate>20170101</enddate><creator>Quirós, Luis M.</creator><creator>Vazquez, Fernando</creator><creator>Lisa, Carlos</creator><creator>González, Javier</creator><creator>Alcalde, Ignacio</creator><creator>Ferrara, Guilherme</creator><creator>Merayo-Lloves, Jesús</creator><creator>García-Suárez, Olivia</creator><creator>García, Beatriz</creator><creator>Alfonso, Jose F.</creator><general>Hindawi Publishing Corporation</general><general>Hindawi</general><general>John Wiley & Sons, Inc</general><general>Hindawi Limited</general><scope>ADJCN</scope><scope>AHFXO</scope><scope>RHU</scope><scope>RHW</scope><scope>RHX</scope><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>7QL</scope><scope>7QO</scope><scope>7TK</scope><scope>8FD</scope><scope>C1K</scope><scope>FR3</scope><scope>P64</scope><scope>RC3</scope><scope>7X8</scope><scope>5PM</scope><orcidid>https://orcid.org/0000-0002-0373-8209</orcidid><orcidid>https://orcid.org/0000-0003-3505-3762</orcidid></search><sort><creationdate>20170101</creationdate><title>Heparanase Overexpresses in Keratoconic Cornea and Tears Depending on the Pathologic Grade</title><author>Quirós, Luis M. ; Vazquez, Fernando ; Lisa, Carlos ; González, Javier ; Alcalde, Ignacio ; Ferrara, Guilherme ; Merayo-Lloves, Jesús ; García-Suárez, Olivia ; García, Beatriz ; Alfonso, Jose F.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c525t-d3ecb1747be0b860d9cc138228d69e16332335ca850e4ef289e177cae3c93e123</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2017</creationdate><topic>Biological markers</topic><topic>Biomarkers</topic><topic>Biomarkers - metabolism</topic><topic>Catalysis</topic><topic>Catalytic activity</topic><topic>Cells, Cultured</topic><topic>Control methods</topic><topic>Cornea</topic><topic>Cornea - enzymology</topic><topic>Cornea - metabolism</topic><topic>Enzymatic activity</topic><topic>Epithelial cells</topic><topic>Gene expression</topic><topic>Genetic aspects</topic><topic>Glucuronidase - genetics</topic><topic>Glucuronidase - metabolism</topic><topic>Heparan sulfate</topic><topic>Heparitin Sulfate - metabolism</topic><topic>Humans</topic><topic>Immunohistochemistry</topic><topic>Inflammatory diseases</topic><topic>Keratoconus</topic><topic>Keratoconus - enzymology</topic><topic>Keratoconus - metabolism</topic><topic>Keratoconus - pathology</topic><topic>Polymerase chain reaction</topic><topic>Substrates</topic><topic>Sulfates</topic><topic>Tears</topic><topic>Tears - enzymology</topic><topic>Tears - metabolism</topic><topic>Transcription</topic><topic>Up-Regulation</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Quirós, Luis M.</creatorcontrib><creatorcontrib>Vazquez, Fernando</creatorcontrib><creatorcontrib>Lisa, Carlos</creatorcontrib><creatorcontrib>González, Javier</creatorcontrib><creatorcontrib>Alcalde, Ignacio</creatorcontrib><creatorcontrib>Ferrara, Guilherme</creatorcontrib><creatorcontrib>Merayo-Lloves, Jesús</creatorcontrib><creatorcontrib>García-Suárez, Olivia</creatorcontrib><creatorcontrib>García, Beatriz</creatorcontrib><creatorcontrib>Alfonso, Jose F.</creatorcontrib><collection>الدوريات العلمية والإحصائية - e-Marefa Academic and Statistical Periodicals</collection><collection>معرفة - المحتوى العربي الأكاديمي المتكامل - e-Marefa Academic Complete</collection><collection>Hindawi Publishing Complete</collection><collection>Hindawi Publishing Subscription Journals</collection><collection>Hindawi Publishing Open Access</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Bacteriology Abstracts (Microbiology B)</collection><collection>Biotechnology Research Abstracts</collection><collection>Neurosciences Abstracts</collection><collection>Technology Research Database</collection><collection>Environmental Sciences and Pollution Management</collection><collection>Engineering Research Database</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>Genetics Abstracts</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Disease markers</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Quirós, Luis M.</au><au>Vazquez, Fernando</au><au>Lisa, Carlos</au><au>González, Javier</au><au>Alcalde, Ignacio</au><au>Ferrara, Guilherme</au><au>Merayo-Lloves, Jesús</au><au>García-Suárez, Olivia</au><au>García, Beatriz</au><au>Alfonso, Jose F.</au><au>Theocharis, Stamatios E.</au><au>Stamatios E Theocharis</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Heparanase Overexpresses in Keratoconic Cornea and Tears Depending on the Pathologic Grade</atitle><jtitle>Disease markers</jtitle><addtitle>Dis Markers</addtitle><date>2017-01-01</date><risdate>2017</risdate><volume>2017</volume><issue>2017</issue><spage>1</spage><epage>7</epage><pages>1-7</pages><issn>0278-0240</issn><eissn>1875-8630</eissn><abstract>Background. Keratoconus has classically been defined as a noninflammatory disorder, although recent studies show elevated levels of inflammatory markers suggesting that keratoconus could be, at least in part, an inflammatory condition. Heparanase upregulation has been described in multiple inflammatory disorders. In this article, we study the differential expression of heparanase in cornea and tears from keratoconus patients and healthy controls. Methods. A transcriptomic approach was used employing quantitative polymerase chain reaction to analyze the expression of heparanase and heparanase 2 in stromal and epithelial corneal cells. The protein expression was analyzed by immunohistochemistry in corneal sections. Enzymatic activity in tears was measured using [3H]-labeled heparan sulfate as substrate. Results. Heparanase transcription was detected in stromal and epithelial cells and appeared upregulated in keratoconus. Overexpression of the enzyme was also detected by immunohistochemistry. Corneal expression of heparanase 2 was detected in some cases. Heparanase catalytic activity was found in tears and displayed a positive correlation with the degree of keratoconus. Conclusions. Heparanase overexpresses in keratoconic corneas, possibly reinforcing the inflammatory condition of the pathology. The presence of heparanase activity in tears allows us to propose its use as a biomarker for the diagnosis of the disorder.</abstract><cop>Cairo, Egypt</cop><pub>Hindawi Publishing Corporation</pub><pmid>29379222</pmid><doi>10.1155/2017/3502386</doi><tpages>7</tpages><orcidid>https://orcid.org/0000-0002-0373-8209</orcidid><orcidid>https://orcid.org/0000-0003-3505-3762</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | Biological markers Biomarkers Biomarkers - metabolism Catalysis Catalytic activity Cells, Cultured Control methods Cornea Cornea - enzymology Cornea - metabolism Enzymatic activity Epithelial cells Gene expression Genetic aspects Glucuronidase - genetics Glucuronidase - metabolism Heparan sulfate Heparitin Sulfate - metabolism Humans Immunohistochemistry Inflammatory diseases Keratoconus Keratoconus - enzymology Keratoconus - metabolism Keratoconus - pathology Polymerase chain reaction Substrates Sulfates Tears Tears - enzymology Tears - metabolism Transcription Up-Regulation |
title | Heparanase Overexpresses in Keratoconic Cornea and Tears Depending on the Pathologic Grade |
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