November 1990
Volume 31, Issue 11
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Articles  |   November 1990
Calcium-induced opacification and proteolysis in the intact rat lens.
Author Affiliations
  • R J Truscott
    Australian Cataract Research Foundation, University of Wollongong, New South Wales.
  • J M Marcantonio
    Australian Cataract Research Foundation, University of Wollongong, New South Wales.
  • J Tomlinson
    Australian Cataract Research Foundation, University of Wollongong, New South Wales.
  • G Duncan
    Australian Cataract Research Foundation, University of Wollongong, New South Wales.
Investigative Ophthalmology & Visual Science November 1990, Vol.31, 2405-2411. doi:
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      R J Truscott, J M Marcantonio, J Tomlinson, G Duncan; Calcium-induced opacification and proteolysis in the intact rat lens.. Invest. Ophthalmol. Vis. Sci. 1990;31(11):2405-2411.

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Abstract

When intact rat lenses were incubated in artificial aqueous humor in the presence of 1 mM calcium and a sulfhydryl reagent p-chloromercuriphenyl sulfonate (pCMPS) a visible annular opacity developed within 4 hours. Combined photographic and ion-sensitive microelectrode investigations of the lenses demonstrated that the subsequent linear increase in opacification was accompanied by an increase in internal free calcium. Opacities were not observed in lenses incubated in the absence of either pCMPS or calcium. Gel electrophoresis of the soluble and urea-soluble fractions from lenses exposed to 1 mM calcium for periods of up to 14 hours showed no evidence for crystallin degradation and only minor proteolysis of cytoskeletal proteins. When lenses were incubated under identical conditions, but with 5 mM calcium, the degree of opacification increased up to approximately 8 hours and then remained constant. A progressive loss in cytoskeletal proteins was observed which correlated with a further increase in free calcium such that by 14 hours of incubation, when the internal calcium approached 1 mM, most of the spectrin and vimentin present in the cortex of the lens had disappeared. An unidentified 110-kilodalton protein also disappeared from lenses incubated in 5 mM calcium. These results indicate that proteolysis by calcium-dependent enzymes such as calpain may play a significant role in cytoskeletal regulation and metabolism in the lens. A role for cytoskeleton/membrane/crystallin interaction in calcium-induced opacification is discussed.

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