Literature DB >> 8670754

Fiber cell morphology and cytoplasmic texture in cataractous and normal human lens nuclei.

K J al-Ghoul1, M J Costello.   

Abstract

PURPOSE: The goal of this study was to compare the ultrastructure of the oldest cells in opaque and transparent human lenses.
METHODS: Age-related nuclear cataracts, late-onset diabetic nuclear cataracts and normal aged lenses were examined by transmission electron microscopy. Cross-sectional profiles of fiber cells in the embryonic, fetal and juvenile nuclear regions were obtained to facilitate direct comparisons between lens regions and between sample groups. Image analysis was performed to determine cross-sectional areas of fiber cells in each region.
RESULTS: The average cross-sectional area increased approximately sixfold from the outer to the inner nuclear regions in all lenses measured. In each nuclear region, fiber cells displayed a characteristic size, shape, arrangement and type of interdigitations which were consistently seen in all the lenses examined. Some lenses had more complex interdigitations than others. Gap junctions were identified as pentalamellar structures having 16 nm width and appeared identical throughout the nuclei of both normal and cataractous lenses. The cytoplasm of all lenses was smooth and free of large density variations. However, the cytoplasm of some cataractous lenses appeared more granular in texture than noncataractous lenses. Cellular degeneration, debris or large cellular defects were not seen in the cores of cataractous lens nuclei.
CONCLUSIONS: These results indicate that only minor ultrastructural differences exist between the oldest fiber cells in normal and cataractous lenses, and that the presence of extensive cellular damage and disruptions is not necessary for the generation of nuclear opacities in aged lenses. Our observations suggest that light scattering sufficient for vision impairment may involve structural alterations much smaller than previously proposed.

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Year:  1996        PMID: 8670754     DOI: 10.3109/02713689609000764

Source DB:  PubMed          Journal:  Curr Eye Res        ISSN: 0271-3683            Impact factor:   2.424


  18 in total

1.  Deficiency of the RNA binding protein caprin2 causes lens defects and features of Peters anomaly.

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2.  Aggregation of lens crystallins in an in vivo hyperbaric oxygen guinea pig model of nuclear cataract: dynamic light-scattering and HPLC analysis.

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3.  Multilamellar spherical particles as potential sources of excessive light scattering in human age-related nuclear cataracts.

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Review 4.  The ageing lens and cataract: a model of normal and pathological ageing.

Authors:  R Michael; A J Bron
Journal:  Philos Trans R Soc Lond B Biol Sci       Date:  2011-04-27       Impact factor: 6.237

5.  Autosomal recessive congenital cataract in consanguineous Pakistani families is associated with mutations in GALK1.

Authors:  Afshan Yasmeen; S Amer Riazuddin; Haiba Kaul; Sadia Mohsin; Mohsin Khan; Zaheeruddin A Qazi; Idrees A Nasir; Ahmad U Zafar; Shaheen N Khan; Tayyab Husnain; Javed Akram; J Fielding Hejtmancik; Sheikh Riazuddin
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6.  Aberrant basal fiber end migration underlies structural malformations in a streptozotocin-induced diabetic rat model.

Authors:  Anita Joy; Matthew S Currie; Sean T Donohue; Kristin J Al-Ghoul
Journal:  Exp Eye Res       Date:  2009-04-07       Impact factor: 3.467

7.  The structure of the cytoplasm of lens fibers as determined by conical tomography.

Authors:  C Schietroma; N Fain; L M Zampighi; S Lanzavecchia; G A Zampighi
Journal:  Exp Eye Res       Date:  2008-12-10       Impact factor: 3.467

8.  Analysis of nuclear fiber cell cytoplasmic texture in advanced cataractous lenses from Indian subjects using Debye-Bueche theory.

Authors:  S Metlapally; M J Costello; K O Gilliland; B Ramamurthy; P V Krishna; D Balasubramanian; S Johnsen
Journal:  Exp Eye Res       Date:  2007-12-05       Impact factor: 3.467

9.  Mapping of a new locus associated with autosomal recessive congenital cataract to chromosome 3q.

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Journal:  Mol Vis       Date:  2010-12-08       Impact factor: 2.367

10.  A new locus for autosomal recessive congenital cataract identified in a Pakistani family.

Authors:  Haiba Kaul; S Amer Riazuddin; Afshan Yasmeen; Sadia Mohsin; Mohsin Khan; Idrees A Nasir; Shaheen N Khan; Tayyab Husnain; Javed Akram; J Fielding Hejtmancik; Sheikh Riazuddin
Journal:  Mol Vis       Date:  2010-02-16       Impact factor: 2.367

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