| Literature DB >> 23727510 |
S Li1, Z C Liu, S J Yin, Y T Chen, H L Yu, J Zeng, Q Zhang, F Zhu.
Abstract
Numerous studies have shown that human endogenous retrovirus W family (HERV-W) envelope gene (env) is related to various diseases but the underlying mechanism has remained poorly understood. Our previous study showed that there was abnormal expression of HERV-W env in sera of patients with schizophrenia. In this paper, we reported that overexpression of the HERV-W env elevated the levels of small conductance Ca(2+)-activated K(+) channel protein 3 (SK3) in human neuroblastoma cells. Using a luciferase reporter system and RNA interference method, we found that functional cAMP response element site was required for the expression of SK3 triggered by HERV-W env. In addition, it was also found that the SK3 channel was activated by HERV-W env. Further study indicated that cAMP response element-binding protein (CREB) was required for the activation of the SK3 channel. Thus, a novel signaling mechanism of how HERV-W env influences neuronal activity and contributes to mental illnesses such as schizophrenia was proposed.Entities:
Keywords: CRE; CREB; Ca(2+)-activated K(+); ENV; HERV; HERV-W; KCa; RT-PCR; SK; SK3; ScyTX; cAMP response element; cAMP response element-binding protein; cAMP response element-binding protein (CREB); env; envelope gene; envelope protein; human endogenous retrovirus; human endogenous retrovirus W family; human endogenous retrovirus W family envelope gene (HERV-W env); pCREB; phosphorylated CREB; reverse transcriptase-polymerase chain reaction; schizophrenia; scyllatoxin; shRNA; short hairpin RNA; small Ca(2+)-activated K(+); small conductance Ca(2+)-activated K(+) channel protein 3; small conductance Ca(2+)-activated K(+) channel protein 3 (SK3)
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Year: 2013 PMID: 23727510 DOI: 10.1016/j.neuroscience.2013.05.033
Source DB: PubMed Journal: Neuroscience ISSN: 0306-4522 Impact factor: 3.590