2008
DOI: 10.1167/iovs.08-1674
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Interactions between Trabecular Meshwork Cells and Lens Epithelial Cells: A Possible Mechanism in Infantile Aphakic Glaucoma

Abstract: Many of the changes observed in TM cells after exposure to LECs resemble alternations seen in primary open-angle glaucoma. This strengthens the suspected role of LECs in the development of aphakic glaucoma.

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Cited by 39 publications
(20 citation statements)
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References 32 publications
(24 reference statements)
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“…Early or incipient opacities consist of cohorts of disorganized lens fibre cells located in the deep equatorial cortex of the lens and characterized by a high content of phospholipids, cholesterol, disulphide cross‐linked proteins and free Ca ++ (Vrensen 2009). In a recent article, Michael et al. (2008) emphasized that the early opacities are the precursors of a common type of cataract: age‐related cuneiform cortical cataract.…”
Section: Resultsmentioning
confidence: 99%
“…Early or incipient opacities consist of cohorts of disorganized lens fibre cells located in the deep equatorial cortex of the lens and characterized by a high content of phospholipids, cholesterol, disulphide cross‐linked proteins and free Ca ++ (Vrensen 2009). In a recent article, Michael et al. (2008) emphasized that the early opacities are the precursors of a common type of cataract: age‐related cuneiform cortical cataract.…”
Section: Resultsmentioning
confidence: 99%
“…The COL11A1 gene codes for one of the two α-chains of type XI collagen, a minor fibril-forming collagen that controls fibril growth, diameter, and assembly of major collagens. This gene is expressed primarily in the articular cartilage and the ocular vitreous [26], as well as the trabecular meshwork [27]. Mutations in COL11A1 cause disorders characterized by midfacial hypoplasia, sensorineural-hearing deficit, and nonprogressive axial myopia [28], such as Marshall syndrome, Stickler syndrome, and Stickler-like syndrome.…”
Section: Discussionmentioning
confidence: 99%
“…The COL11A1 gene also has been implicated in the regulation of the drainage of aqueous humor with evidence of its expression in human trabecular meshwork cells. 14 The SNP rs1015213 is located between PCMTD1 and ST18. The PCMTD1 gene encodes protein-L-isoaspartate O-methyltransferase domain-containing protein 1 and its function is largely unknown.…”
Section: Discussionmentioning
confidence: 99%