Tear film proteome changes following Tobradex® therapy in anterior blepharitis

Author:

Muttuvelu Danson Vasanthan1ORCID,Cehofski Lasse Jørgensen23ORCID,Utheim Tor Paaske45,Chen Xiangjun5ORCID,Vorum Henrik67,Rasmussen Marie Louise Roed8,Heegaard Steffen8ORCID,Khan Asif Manzoor9,Abduljabar Ahmed Basim9,Honoré Bent79

Affiliation:

1. Faculty of Health and Medical Sciences University of Copenhagen Copenhagen Denmark

2. Department of Ophthalmology Odense University Hospital Odense Denmark

3. Department of Clinical Research University of Southern Denmark Odense Denmark

4. Department of Medical Biochemistry Oslo University Hospital Oslo Norway

5. The Norwegian Dry Eye Clinic Oslo Norway

6. Department of Ophthalmology Aalborg University Hospital Aalborg Denmark

7. Department of Clinical Medicine Aalborg University Aalborg Denmark

8. Department of Ophthalmology, Rigshospitalet University of Copenhagen Copenhagen Denmark

9. Department of Biomedicine Aarhus University Aarhus Denmark

Abstract

AbstractPurposeThe management of blepharitis continues to challenge clinicians due to the poorly understood aetiology of the condition. We recently identified the family of intracellular plakin proteins as essential driving forces underlying anterior blepharitis. A large‐scale protein analysis was used to study if a topical dexamethasone/tobramycin solution could be used to reverse the expression of plakin proteins.MethodsTear film samples from treatment naïve patients with anterior blepharitis (n = 15) were collected with Schirmer filtration paper. A subgroup of the patients (n = 10) received treatment with a dexamethasone/tobramycin 1 + 3 mg/mL ophthalmic suspension (Tobradex®) for 3 weeks and collection of tear film samples was repeated. The samples were analysed with label‐free quantification nano liquid chromatography–tandem mass spectrometry requiring quantification in at least 70% of the samples in each group. Proteins were considered differentially expressed if p < 0.05.ResultsFollowing Tobradex® intervention, 27 proteins were upregulated while 61 proteins were downregulated. Regulated proteins after Tobradex® treatment were involved in intermediate filament cytoskeleton organization including downregulation of the plakin proteins envoplakin, epiplakin and periplakin. Plectin, a protein of the plakin family, remained unchanged after Tobradex® therapy. Tobradex® treatment resulted in the regulation of proteins involved in translation including a cluster of downregulated ribosomal proteins. Tobradex® intervention was associated with the regulation of proteins involved in fructose metabolism and glycolytic processes including fructose‐1.6‐bisphosphatase 1, fructose‐bisphosphate aldolases A and B, pyruvate kinase PKM and transketolase. Ig lambda chain V‐I region, prominin‐1, and protein Niban were upregulated after Tobradex® treatment.ConclusionsTobradex treatment reversed the expression of plakin proteins in anterior blepharitis. Topical solutions which inhibit the expression of plakin proteins may have the potential to restore the ocular surface integrity in anterior blepharitis and should be explored further.

Publisher

Wiley

Subject

Ophthalmology,General Medicine

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