| Literature DB >> 19635392 |
Jiangong Liu1, Ran Zhou, Quanren He, Wan-I Li, Ting Zhang, Bo Niu, Xiaoying Zheng, Jun Xie.
Abstract
Previous studies have shown that apoptosis can be mediated by activation of either calmodulin kinase II (CaMKII) or mitogen-activated protein kinase (MAPK), ERK and p38. In the present study, we investigated whether CaMKII is involved in activation of ERK and p38 in response to all-trans retinoic acid (ATRA) treatment in PC12 cells. Results showed that ATRA-induced activation of ERK and p38 occurred later than that of CAMKII. Knockdown of CAMKII by siRNA significantly suppressed ATRA-induced activation of ERK and p38. These results demonstrated that activation of ERK and p38 following ATRA exposure is CAMKII-dependent. Treatment with ATRA also resulted in cell death characterized by apoptosis in PC12 cells. Results suggest that CaMKII-dependent activation of ERK and p38 is related to apoptotic cell death.Entities:
Mesh:
Substances:
Year: 2009 PMID: 19635392 DOI: 10.1016/j.neuro.2009.03.006
Source DB: PubMed Journal: Neurotoxicology ISSN: 0161-813X Impact factor: 4.294