OUTLINE Introduction Materials and Methods Patient Selection Tear Sample Collection Saliva Sample Collection Glycan Release Glycan Enrichment Mass Spectrometric Analysis Results Discussion Conclusion GLYCOSYLATION IN TEAR AND SALIVA OF OCULAR ROSACEA

The purpose of this study was to study changes in glycosylation in tear and saliva obtained from control and ocular rosacea patients in order to identify potential biomarkers for rosacea. Tear fluid was collected from 51 subjects (28 healthy controls and 23 patients with ocular rosacea). Saliva was collected from 42 of the same subjects (25 controls and 17 patients). Pooled and individual samples were examined to determine overall glycan profiles and individual variations in glycosylation. O-and Nglycans were released from both patients and control subjects. Released glycans were purified and enriched by solid-phase extraction (SPE) with graphitized carbon. Glycans were eluted based on glycan size and polarity. SPE fractions were then analyzed by high-resolution mass spectrometry. Glycan compositions were assigned by accurate masses. Their structures were further elucidated by tandem mass spectrometric using collision-induced dissociation (CID), and specific linkage information was obtained by exoglycosidase digestion. Nand O-glycans were released from 20-mL samples without protein identification, separation, and purification. Approximately 50 N-glycans and 70 O-glycans were globally profiled Accepted for publication April 2012. From the Department of Ophthalmology, University of California, Davis, CA, Department of Ophthalmology, São Paulo Hospital, Federal University of São Paulo, Brazil, Department of Chemistry, University of California, Davis, CA, Department of Viticulture and Enology, University of California, Davis, CA, and Department of Biochemistry and Molecular Medicine, University of California, Davis, CA, USA. Financial Support: This study was funded in part by Research to Prevent Blindness, Inc., New York, NY, and by CAPES (Brazil) grant to ACV. The sponsor or funding organizations had no role in the design or conduct of this research. The authors have no commercial or proprietary interest in any concept or product discussed in this article. Single-copy reprint requests to Mark Mannis, MD (address below). Corresponding author: Mark J. Mannis, MD, Department of Ophthalmology eUniversity of California, Davis, 4860 Y Street, Suite 2400, Sacramento, CA 95817. Tel: (916)734-6957. Fax: (916)703-5076. E-mail address: mjmannis@ ucdavis.edu © 2012 Elsevier Inc. All rights reserved. The Ocular Surface ISSN: 15420124. Vieira AC, An HJ, Ozcan S, Kim JH, Lebrilla CB, Mannis MJ. Glycomic analysis of tear and saliva in ocular rosacea patients: The search for a biomarker. 2012;10(3):184-192. 184 THE OCULAR SURFACE / JULY 2012, V by mass spectrometry. Most N-glycans were highly fucosylated, while O-glycans were sulfated. Normal tear fluid and saliva contain highly fucosylated glycans. The numbers of sulfated glycans were dramatically increased in tear and saliva of rosacea patients compared to controls. Glycans found in tear and saliva from roseatic patients present highly quantitative similarity. The abundance of highly fucosylated N-glycans in the control samples and sulfated O-glycans in ocular rosacea patient samples may lead to the discovery of an objective diagnostic marker for the disease.

[1]  Niclas G Karlsson,et al.  The glycosylation of human synovial lubricin: implications for its role in inflammation. , 2010, The Biochemical journal.

[2]  Scott R. Kronewitter,et al.  Glycomics and disease markers. , 2009, Current opinion in chemical biology.

[3]  Yi Wei,et al.  Analysis of Inflammatory Cytokines in the Tears of Dry Eye Patients , 2009, Cornea.

[4]  Scott R. Kronewitter,et al.  Glycomic Approach for Potential Biomarkers on Prostate Cancer: Profiling of N-Linked Glycans in Human Sera and pRNS Cell Lines , 2009, Disease markers.

[5]  F. Mantelli,et al.  Functions of ocular surface mucins in health and disease , 2008, Current opinion in allergy and clinical immunology.

[6]  Joseph Zaia,et al.  Mass spectrometry and the emerging field of glycomics. , 2008, Chemistry & biology.

[7]  I. Gipson,et al.  Release of membrane-associated mucins from ocular surface epithelia. , 2008, Investigative ophthalmology & visual science.

[8]  S. Delaney,et al.  Mite‐related bacterial antigens stimulate inflammatory cells in rosacea , 2007, The British journal of dermatology.

[9]  A. Hovnanian,et al.  Increased serine protease activity and cathelicidin promotes skin inflammation in rosacea , 2007, Nature Medicine.

[10]  Kit S. Lam,et al.  A Serum Glycomics Approach to Breast Cancer Biomarkers*S , 2007, Molecular & Cellular Proteomics.

[11]  Kit S Lam,et al.  Profiling of glycans in serum for the discovery of potential biomarkers for ovarian cancer. , 2006, Journal of proteome research.

[12]  C. Lebrilla,et al.  Glycomics analyses of tear fluid for the diagnostic detection of ocular rosacea. , 2005, Journal of proteome research.

[13]  W. James,et al.  Rosacea: I. Etiology, pathogenesis, and subtype classification. , 2004, Journal of the American Academy of Dermatology.

[14]  Serena Wong,et al.  The prevalence of ocular signs in acne rosacea: comparing patients from ophthalmology and dermatology clinics. , 2003 .

[15]  R. Dana,et al.  Decreased levels of the goblet cell mucin MUC5AC in tears of patients with Sjögren syndrome. , 2002, Investigative ophthalmology & visual science.

[16]  A. Feinstein,et al.  Standard classification of rosacea: Report of the National Rosacea Society Expert Committee on the Classification and Staging of Rosacea. , 2002, Journal of the American Academy of Dermatology.

[17]  I. Lamster,et al.  The diagnostic applications of saliva--a review. , 2002, Critical reviews in oral biology and medicine : an official publication of the American Association of Oral Biologists.

[18]  S. Batra,et al.  Structural organization and classification of the human mucin genes. , 2001, Frontiers in bioscience : a journal and virtual library.

[19]  S. Georgala,et al.  Increased density of Demodex folliculorum and evidence of delayed hypersensitivity reaction in subjects with papulopustular rosacea , 2001, Journal of the European Academy of Dermatology and Venereology : JEADV.

[20]  A. Solomon,et al.  Pro- and anti-inflammatory forms of interleukin-1 in the tear fluid and conjunctiva of patients with dry-eye disease. , 2001, Investigative ophthalmology & visual science.

[21]  L. Sobrin,et al.  Regulation of MMP-9 activity in human tear fluid and corneal epithelial culture supernatant. , 2000, Investigative ophthalmology & visual science.

[22]  E. Karczewska,et al.  Helicobacter pylori and its eradication in rosacea. , 1999, Journal of physiology and pharmacology : an official journal of the Polish Physiological Society.

[23]  C. Utaş,et al.  Helicobacter pylori eradication treatment reduces the severity of rosacea. , 1999, Journal of the American Academy of Dermatology.

[24]  F. Morel,et al.  Gelatinase concentration in tears of corneal-grafted patients. , 1998, Current eye research.

[25]  E. Veerman,et al.  Salivary mucins: protective functions in relation to their diversity. , 1995, Glycobiology.

[26]  A. Guzman-Aranguez,et al.  Structure and biological roles of mucin-type O-glycans at the ocular surface. , 2010, The ocular surface.

[27]  Carlito B. Lebrilla,et al.  The prospects of glycan biomarkers for the diagnosis of diseases. , 2009, Molecular bioSystems.

[28]  D. Pahor,et al.  [Repair of an extensive corneoscleral perforation in a case of ocular rosacea with a keratoplasty]. , 2006, Klinische Monatsblatter fur Augenheilkunde.

[29]  L. S. Alvarenga,et al.  Ocular rosacea. , 2005, The ocular surface.

[30]  C. O'Callaghan,et al.  Rosacea: a cutaneous marker of Helicobacter pylori infection? Results of a pilot study. , 2003, Acta dermato-venereologica.

[31]  I. Gipson,et al.  The cell-layer- and cell-type-specific distribution of GalNAc-transferases in the ocular surface epithelia is altered during keratinization. , 2003, Investigative ophthalmology & visual science.

[32]  L. Tabak,et al.  Role of salivary mucins in the protection of the oral cavity. , 1982, Journal of oral pathology.