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Involvement of calpain 2 in ionomycin-induced cell death in cultured mouse lens epithelial cells
Takeshi Nakajima; Thomas R. Shearer; Mitsuyoshi Azuma (Profiled Author: Thomas (Tom) Shearer)
Current Eye Research. 2011;36(10):930-936.
AbstractPurpose: Calpains are calcium-activated, intracellular, non-lysosomal, cysteine proteases that hydrolyze lens crystallins and cytoskeletal proteins. Elevated calcium is a frequent finding in both rodent and human cataracts, and calpain 2 is present in lenses of both species. Lens epithelium forms a critical barrier to influx of calcium, but the role of calpain 2 in lens epithelium is poorly characterized. Thus, the purpose of the present experiment was to determine the role of calpain 2 in lens epithelial cell death. Methods: Mouse lens epithelial cells (α-TN4) were cultured with the calcium ionophore ionomycin to promote calcium influx. Release of LDH into the culture medium was measured as a general marker of cell death, while necrosis and apoptosis were detected by staining with ethidium homodimer III (EtD-III) or FITC-annexin V. Calpain activity was determined by zymography and immunoblotting for activation-associated, fragments of calpain. Breakdown products of calpain substrate α-spectrin were also detected by immunoblotting as additional markers of calpain activation. Results: Calpain 2 was found to be the major calpain isozyme in α-TN4 cells. Ionomycin caused leakage of LDH into the medium, activation of calpain 2, proteolysis of α-spectrin, and changes in α-TN4 cell morphology and staining characteristic of necrotic cell death. Calpain inhibitor SNJ-1945 significantly inhibited these changes. Conclusions: The ability of mouse lens epithelium to maintain lens transparency would be compromised by activation of calpain 2 and associated necrotic cell death. Since calpain 2 is ubiquitously present in all animal lenses so far observed, the current results may predict the pathological consequences of calpain 2 activation in animal lenses including those of man. © 2011 Informa Healthcare USA, Inc.
PMID: 21950698
Scientific Context
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Related Publications
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1.
2000Y. Tamada; C. Fukiage; Y. Nakamura; M. Azuma; Y.H. Kim; T.R. Shearer
Evidence for apoptosis in the selenite rat model of cataract
Biochemical and Biophysical Research Communications. 2000;275(2):300-306. -
2.
2007Takayuki Oka; Takeshi Nakajima; Yoshiyuki Tamada; Thomas R. Shearer; Mitsuyoshi Azuma
Contribution of calpains to photoreceptor cell death in N-methyl-N-nitrosourea-treated rats
Experimental Neurology. 2007;204(1):39-48. -
3.
1991T.R. Shearer; M. Azuma; L.L. David; T. Murachi
Amelioration of cataracts and proteolysis in cultured lenses by cysteine protease inhibitor E64
Investigative Ophthalmology and Visual Science. 1991;32(3):533-540.
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