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Published on: October 4, 2019
Decreased corneal biomechanical stability and structural integrity in PPAR-α knockout mice
Chengfang Zhu1, Huan He2, Hongwei Yan3
1Eye Institute and Affiliated Xiamen Eye Center of Xiamen University, School of Medicine, Xiamen University, Xiamen, China; Affiliated Hospital of Putian University, China.
Mice lacking peroxisome proliferator-activated receptor-α (PPAR-α) exhibit reduced corneal biomechanical stability and microstructural integrity. This decline is linked to altered corneal components, inflammation, and protease activity.
Area of Science:
- Ophthalmology
- Biomaterials Science
- Molecular Biology
Background:
- Corneal biomechanical failure is linked to inflammatory cytokines and proteolytic enzymes.
- Peroxisome proliferator-activated receptor-α (PPAR-α) activation may inhibit inflammatory cascades.
Purpose of the Study:
- Investigate corneal biomechanical and structural features in PPAR-α-/- mice.
- Assess alterations in inflammatory cytokines and enzymes in PPAR-α-/- mice.
Main Methods:
- Evaluated corneas from PPAR-α-/- and wild-type mice using elasticity tests, enzymatic digestion, OCT, IVCM, TEM, and RT-PCR.
- Assessed tear film break-up time (tBUT) and corneal fluorescein sodium staining.
Main Results:
- PPAR-α-/- mice showed decreased corneal tangent modulus, enzymatic resistance, and thinner corneas.
- Microscopy revealed disorganized stromal fibers and reduced density in PPAR-α-/- mice.
- Gene expression analysis indicated decreased structural proteins and increased inflammatory markers (TNF-α, MMP-9) in PPAR-α-/- corneas.
Conclusions:
- PPAR-α deficiency compromises corneal biomechanical stability and microstructural integrity.
- Dysregulation of structural components, inflammatory factors, and proteases contributes to corneal alterations in PPAR-α-/- mice.
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