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Updated: Jul 30, 2026

Trabecular Meshwork Response to Pressure Elevation in the Living Human Eye
Published on: June 20, 2015
Time-dependent Glucocorticoid-Induced Transcriptomic Changes in Human Trabecular Meshwork and Schlemm's Canal
Sudeep Mehrotra1,2, Haven Jeanneret3, Kristin Perkumas4
1Department of Ophthalmology, Massachusetts Eye and Ear Infirmary.
Dexamethasone (DEX) alters gene expression in trabecular meshwork and Schlemm
Area of Science:
- Ocular biology
- Transcriptomics
- Glaucoma research
Background:
- Glucocorticoids, like dexamethasone (DEX), are widely used but can cause ocular hypertension.
- The molecular mechanisms underlying DEX-induced ocular hypertension in the trabecular meshwork (TM) and Schlemm's canal endothelial (SCE) cells are not fully understood.
Purpose of the Study:
- To investigate the transcriptomic alterations induced by DEX in human TM and SCE cells using RNA-sequencing (RNA-seq).
- To identify genes and pathways involved in DEX-induced changes relevant to intraocular pressure (IOP) and primary open-angle glaucoma (POAG).
Main Methods:
- Human TM (n=10) and SCE (n=5) cell strains were treated with DEX (100nM) or vehicle for 1 hour, 6 hours, and 2 days.
- RNA-sequencing was performed, and differential gene expression analysis was conducted using DESeq2.
- Gene-set enrichment analysis and association testing with POAG and IOP were performed on differentially expressed genes (DEGs).
Main Results:
- After 2-day DEX exposure, 857 DEGs were identified in TM cells and 2,086 in SCE cells.
- 411 genes were differentially expressed in both cell types, including significant upregulation of FKBP5 and FAM107A.
- DEGs were enriched in pathways related to cell adhesion, extracellular matrix, and immune response; early response genes were linked to immune processes.
Conclusions:
- This study identifies key genes and pathways responsive to DEX in TM and SCE cells, providing insights into glucocorticoid-induced ocular hypertension.
- Candidate genes, such as LTBP2 and FAM105A, associated with IOP and POAG risk, were identified.
- The findings offer potential targets for future human genetic analyses related to ocular hypertension.
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