Inhibition of microRNA-328 Increases Ocular Mucin Expression and Conjunctival Goblet Cells

Author:

Choo Jackson1,Liao Chun-Huei2,Tseng Ching-Li34ORCID,Chen Jiunn-Liang5,Cheng Huey-Chuan6,Liang Chung-Ling78,Juo Suh-Hang Hank28910ORCID

Affiliation:

1. Graduate Institute of Biomedical Sciences, China Medical University, Taichung 404, Taiwan

2. Department of Medical Research, China Medical University Hospital, Taichung 404, Taiwan

3. Graduate Institute of Biomedical Materials and Tissue Engineering, College of Biomedical Engineering, Taipei Medical University, Taipei 110, Taiwan

4. International Ph.D. Program in Biomedical Engineering, College of Biomedical Engineering, Taipei Medical University, Taipei 110, Taiwan

5. Department of Ophthalmology, Kaohsiung Veterans General Hospital, Kaohsiung 813, Taiwan

6. Department of Ophthalmology, Mackay Memorial Hospital, Taipei 104, Taiwan

7. Bright-Eyes Clinic, Kaohsiung 800, Taiwan

8. Dreamhawk Vision Biotech, Inc., Kaohsiung 800, Taiwan

9. Institute of New Drug Development, China Medical University, Taichung 404, Taiwan

10. Drug Development Center, China Medical University, Taichung 404, Taiwan

Abstract

We previously reported anti-miR-328 therapy for dry eye disease (DED). Since decreased mucin secretion is a risk factor for DED, we aimed to explore whether anti-miR-328 affects mucin expression and goblet cells. MiR-328 was increased in goblet cells when they were under desiccating stress or treated with benzalkonium chloride (BAC), both of which are risk factors for DED. Based on bioinformatics tool results, miR-328 was predicted to directly target the transcription factor CREB1 that has been known to promote the expression of mucin5AC. The inhibitory effect of miR-328 on CREB1 was confirmed by the transfection assay. A miR-328 binding site on the CREB1 gene was confirmed by the luciferase assay. Furthermore, anti-miR-328 increased CREB1 and mucin5AC in cultured goblet cells according to qPCR, Western blot, and IF staining experiments. Anti-miR-328 increased mucin5AC secretion from the cultured goblet cells based on an ELISA assay for the cultured medium. Finally, impression cytology data revealed anti-miR-328 increased conjunctival goblet cells in the DED rabbits induced by BAC. In conclusion, anti-miR-328 increases CREB1 expression leading to an increase in mucin5AC production and secretion. Furthermore, anti-miR-328 also increases conjunctival goblet cells. These results warrant the further development of anti-miR-328 therapy for DED.

Funder

National Science and Technology Council

Ministry of Education (MOE) in Taiwan

Higher Education Sprout Project by the Ministry of Education (MOE) in Taiwan

Publisher

MDPI AG

Subject

General Biochemistry, Genetics and Molecular Biology,Medicine (miscellaneous)

Reference30 articles.

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