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Laser Capture Microdissection of Highly Pure Trabecular Meshwork from Mouse Eyes for Gene Expression Analysis
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Differential Protein Expression Profiles in Glaucomatous Trabecular Meshwork: An Evaluation Study on a Small Primary
Alessandra Micera1, Luciano Quaranta2, Graziana Esposito1
1IRCCS-G.B. Bietti Foundation, Rome, Italy.
Advances in Therapy
|January 29, 2016
Summary
Primary open angle glaucoma (POAG) involves trabecular meshwork (TM) remodeling. This study identified distinct protein expression patterns in POAG TMs, revealing potential biomarkers for this optic neuropathy.
Area of Science:
- Ophthalmology
- Molecular Biology
- Biochemistry
Background:
- Primary open angle glaucoma (POAG) is a progressive optic neuropathy.
- It is characterized by impaired aqueous humor outflow and trabecular meshwork (TM) remodeling.
- Understanding TM protein expression is crucial for POAG research.
Purpose of the Study:
- To characterize and compare protein expression patterns in ex vivo glaucomatous and post-mortem TMs.
- To investigate proteins involved in tissue remodeling, inflammation, and growth factor pathways.
- To identify potential biomarkers for POAG.
Main Methods:
- Protein-array analysis of TM specimens from 63 subjects (40 POAG, 23 controls).
- Collected 40 POAG TMs during surgery and 23 post-mortem non-glaucomatous TMs.
- Utilized a chip-based array with 60 antibodies; confirmed findings with Western blot, zymography, and PCR.
Main Results:
- Observed differential expression of several proteins in POAG TMs compared to post-mortem TMs.
- Increased abundance of IL10, IL6, IL5, IL7, IL12, IL3, MIP1δ/α, VEGF, TGFβ1, sTNFRI.
- Decreased levels of IL16, IL18, ICAM3, MMP7, TIMP1. MMP2, MMP7, TGFβ1, and VEGF confirmed.
Conclusions:
- Highlighted specific proteins linked to POAG, including novel detections like IL7, MIPs, and sTNFαRI.
- Suggests these proteins may serve as POAG biomarkers.
- Emphasizes the need for larger POAG populations to validate biomarker candidates.
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