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Role of oxidative stress and caspase 3 in CD47‐mediated neuronal cell death
Author(s) -
Xing Changhong,
Lee Sunryung,
Kim Woo Jean,
Jin Guang,
Yang YongGuang,
Ji Xunming,
Wang Xiaoying,
Lo Eng H.
Publication year - 2009
Publication title -
journal of neurochemistry
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.75
H-Index - 229
eISSN - 1471-4159
pISSN - 0022-3042
DOI - 10.1111/j.1471-4159.2008.05777.x
Subject(s) - cd47 , programmed cell death , microbiology and biotechnology , oxidative stress , apoptosis , reactive oxygen species , caspase , free radical scavenger , chemistry , caspase 3 , cell , biology , biochemistry
CD47 or integrin‐associated protein promotes cell death in blood and tumor cells. Recently, CD47 signaling has been identified in neurons as well. In this study, we investigated the role of CD47 in neuronal cell death. Exposure of primary mouse cortical neurons to the CD47 ligand thrombospondin‐1 or the specific CD47‐activating peptide 4N1K induced cell death. Activation of CD47 elevated levels of active caspase 3 and increased the generation of reactive oxygen species (ROS) in a time‐dependent manner. Both ROS scavengers and caspase inhibitors attenuated cell death. But ROS scavenging did not reduce the activation of caspase 3, and combination treatments with a caspase inhibitor plus free radical scavenger did not yield additive protection. Taken together, these data suggest that parallel and redundant pathways of oxidative stress and caspase‐mediated cell death are involved. We conclude that CD47 mediates neuronal cell death through caspase‐dependent and caspase‐independent pathways.