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. 2007 Dec 18;65(2):324–337. doi: 10.1007/s00018-007-7499-7

The cytotoxicity of eosinophil cationic protein/ribonuclease 3 on eukaryotic cell lines takes place through its aggregation on the cell membrane

S Navarro 1, J Aleu 2, M Jiménez 2, E Boix 1, C M Cuchillo 1, M V Nogués 1,
PMCID: PMC11131711  PMID: 18087674

Abstract.

Human eosinophil cationic protein (ECP)/ ribonuclease 3 (RNase 3) is a protein secreted from the secondary granules of activated eosinophils. Specific properties of ECP contribute to its cytotoxic activities associated with defense mechanisms. In this work the ECP cytotoxic activity on eukaryotic cell lines is analyzed. The ECP effects begin with its binding and aggregation to the cell surface, altering the cell membrane permeability and modifying the cell ionic equilibrium. No internalization of the protein is observed. These signals induce cell-specific morphological and biochemical changes such as chromatin condensation, reversion of membrane asymmetry, reactive oxygen species production and activation of caspase-3-like activity and, eventually, cell death. However, the ribonuclease activity component of ECP is not involved in this process as no RNA degradation is observed. In summary, the cytotoxic effect of ECP is attained through a mechanism different from that of other cytotoxic RNases and may be related with the ECP accumulation associated with the inflammatory processes, in which eosinophils are present.

Keywords. Eosinophil cationic protein, ribonuclease, eukaryotic cell cytotoxicity, protein aggregation, cell membrane binding

Footnotes

Received 26 October 2007; accepted 23 November 2007


Articles from Cellular and Molecular Life Sciences: CMLS are provided here courtesy of Springer

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