Navarro S, Aleu J, Jiménez M, Boix E, Cuchillo C M, Nogués M V
Departament de Bioquímica i Biologia Molecular, Universitat Autònoma de Barcelona, 08193, Bellaterra, Spain.
Cell Mol Life Sci. 2008 Jan;65(2):324-37. doi: 10.1007/s00018-007-7499-7.
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.
人嗜酸性粒细胞阳离子蛋白(ECP)/核糖核酸酶3(RNase 3)是一种从活化嗜酸性粒细胞的次级颗粒中分泌的蛋白质。ECP的特定特性有助于其与防御机制相关的细胞毒性活性。在这项工作中,分析了ECP对真核细胞系的细胞毒性活性。ECP的作用始于其与细胞表面的结合和聚集,改变细胞膜通透性并改变细胞离子平衡。未观察到该蛋白质的内化。这些信号诱导细胞特异性的形态和生化变化,如染色质浓缩、膜不对称性逆转、活性氧产生以及半胱天冬酶-3样活性的激活,并最终导致细胞死亡。然而,ECP的核糖核酸酶活性成分不参与此过程,因为未观察到RNA降解。总之,ECP的细胞毒性作用是通过一种不同于其他细胞毒性核糖核酸酶的机制实现的,并且可能与嗜酸性粒细胞存在的炎症过程中ECP的积累有关。