| ORIGINAL ARTICLE |
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| Year : 2019 | Volume
: 62
| Issue : 2 | Page : 63-69 |
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Knockdown of protein kinase CK2 blocked gene expression mediated by brain-derived neurotrophic factor-induced serum response element
Shu-Ping Yang1, Chi-Yi Lo1, Hui-Min Tseng1, Chih-Chang Chao2
1 Institute of Neurosciences, National Chengchi University, Taipei, Taiwan
2 Institute of Neurosciences, National Chengchi University; Research Center for Mind, Brian and Learning, National Chengchi University, Taipei, Taiwan
Correspondence Address:
Dr. Chih-Chang Chao
Institute of Neurosciences, National Chengchi University, Taipei; Research Center for Mind, Brian and Learning, National Chengchi University, Taipei
Taiwan
 Source of Support: None, Conflict of Interest: None
DOI: 10.4103/CJP.CJP_1_19
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One of the principal signaling pathway outcomes from brain-derived neurotrophic factor (BDNF) is the activation of antiapoptotic pathways. In addition to the role of extracellular signal-regulated kinase 1/2 and phosphatidylinositol-3 kinase, BDNF activates protein kinase CK2 to mediate its neuroprotective effect. The inhibition of CK2 activity has been shown to induce apoptosis. Although serum response element (SRE)-mediated transcription has been reported to be activated by BDNF and that the phosphorylation of serum response factor (SRF) by CK2 has been shown to enhance its DNA binding activity, the biological relevance of these interactions remains largely unclear. In the present study, we found that SRE-mediated transcription, CK2 activity, and SRF phosphorylation increased in PC12 cells under BDNF treatment. The transfection of CK2α siRNA blocked the enhancing effect of BDNF on SRE-mediated transcription, SRF phosphorylation, and Mcl-1 gene expression. Moreover, the blockade of CK2 diminished the antiapoptotic effects of BDNF on SRE-mediated transcription, Mcl-1 gene expression, and cell viability under rotenone-induced cytotoxicity. Our data may assist in the development of therapeutic strategies for inhibiting apoptosis during neurodegeneration.
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