Literature DB >> 24076322

Loss of the small heat shock protein αA-crystallin does not lead to detectable defects in early zebrafish lens development.

Mason Posner1, Jackie Skiba, Mary Brown, Jennifer O Liang, Justin Nussbaum, Heather Prior.   

Abstract

Alpha crystallins are small heat shock proteins essential to normal ocular lens function. They also help maintain homeostasis in many non-ocular vertebrate tissues and their expression levels change in multiple diseases of the nervous and cardiovascular system and during cancer. The specific roles that α-crystallins may play in eye development are unclear. Studies with knockout mice suggested that only one of the two mammalian α-crystallins is required for normal early lens development. However, studies in two fish species suggested that reduction of αA-crystallin alone could inhibit normal fiber cell differentiation, cause cataract and contribute to lens degeneration. In this study we used synthetic antisense morpholino oligomers to suppress the expression of zebrafish αA-crystallin to directly test the hypothesis that, unlike mammals, the zebrafish requires αA-crystallin for normal early lens development. Despite the reduction of zebrafish αA-crystallin protein to undetectable levels by western analysis through 4 days of development we found no changes in fiber cell differentiation, lens morphology or transparency. In contrast, suppression of AQP0a expression, previously shown to cause lens cataract, produced irregularly shaped lenses, delay in fiber cell differentiation and lens opacities detectable by confocal microscopy. The normal development observed in αA-crystallin deficient zebrafish embryos may reflect similarly non-essential roles for this protein in the early stages of both zebrafish and mammalian lens development. This finding has ramifications for a growing number of researchers taking advantage of the zebrafish's transparent external embryos to study vertebrate eye development. Our demonstration that lens cataracts can be visualized in three-dimensions by confocal microscopy in a living zebrafish provides a new tool for studying the causes, development and prevention of lens opacities.
Copyright © 2013 Elsevier Ltd. All rights reserved.

Entities:  

Keywords:  alpha crystallin; cataract; lens development; morpholino; ocular lens; small heat shock protein; zebrafish

Mesh:

Substances:

Year:  2013        PMID: 24076322      PMCID: PMC3864005          DOI: 10.1016/j.exer.2013.09.007

Source DB:  PubMed          Journal:  Exp Eye Res        ISSN: 0014-4835            Impact factor:   3.467


  46 in total

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5.  Single cell transcriptomics of the developing zebrafish lens and identification of putative controllers of lens development.

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6.  Transgenic zebrafish models reveal distinct molecular mechanisms for cataract-linked αA-crystallin mutants.

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