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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Veröffentlicht in:Disease markers 2017-01, Vol.2017 (2017), p.1-7
Hauptverfasser: Quirós, Luis M., Vazquez, Fernando, Lisa, Carlos, González, Javier, Alcalde, Ignacio, Ferrara, Guilherme, Merayo-Lloves, Jesús, García-Suárez, Olivia, García, Beatriz, Alfonso, Jose F.
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container_end_page 7
container_issue 2017
container_start_page 1
container_title Disease markers
container_volume 2017
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.
doi_str_mv 10.1155/2017/3502386
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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 &amp; 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. 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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.</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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