期刊
CELLULAR AND MOLECULAR LIFE SCIENCES
卷 67, 期 13, 页码 2271-2281出版社
SPRINGER BASEL AG
DOI: 10.1007/s00018-010-0331-9
关键词
Annexin; Annexin A4; Ca2+; Etoposide; NF-kappa B
资金
- KRIBB
- Korea Research Council of Fundamental Science and Technology
- Korea Science and Engineering Foundation (KOSEF)
- Korean Ministry of Education, Science and Technology
Previously, we identified annexin A4 (ANXA4) as a candidate substrate of caspase-3. Proteomic studies were performed to identify interacting proteins with a view to determining the roles of ANXA4. ANXA4 was found to interact with the p105. Subsequent studies revealed that ANXA4 interacts with NF-kappa B through the Rel homology domain of p50. Furthermore, the interaction is markedly increased by elevated Ca2+ levels. NF-kappa B transcriptional activity assays demonstrated that ANXA4 suppresses NF-kappa B transcriptional activity in the resting state. Following treatment with TNF-alpha or PMA, ANXA4 also suppressed NF-kappa B transcriptional activity, which was upregulated significantly early after etoposide treatment. This difference may be due to the intracellular Ca2+ level. Additionally, ANXA4 translocates to the nucleus together with p50, and imparts greater resistance to apoptotic stimulation by etoposide. Our results collectively indicate that ANXA4 differentially modulates the NF-kappa B signaling pathway, depending on its interactions with p50 and the intracellular Ca2+ ion level.
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