期刊
INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES
卷 19, 期 3, 页码 -出版社
MDPI
DOI: 10.3390/ijms19030796
关键词
vitamin D; TXNIP; VDUP1; cancer
资金
- German Academic Exchange Service (DAAD)
- Deutsche Forschungsgemeinschaft
- Baden-Wurttemberg Ministry of Science, Research and the Arts
- Ruprecht-Karls-Universitat Heidelberg
Thioredoxin-interacting protein (TXNIP) was originally identified in HL-60 cells as the vitamin D-3 upregulated protein 1, and is now known to be involved in diverse cellular processes, such as maintenance of glucose homeostasis, redox balance, and apoptosis. Besides the initial characterization, little is known about if and how 1,25-dihydroxyvitamin D-3 [1,25(OH)(2)D-3] induces TXNIP expression. We therefore screened multiple cancerous cell lines of different tissue origins, and observed induction, repression, or no change in TXNIP expression in response to 1,25(OH)(2)D-3. In-depth analyses on HL-60 cells revealed a rapid and transient increase in TXNIP mRNA levels by 1,25(OH)(2)D-3 (3-24 h), followed by a clear reduction at later time points. Furthermore, a strong induction in protein levels was observed only after 96 h of 1,25(OH)(2)D-3 treatment. Induction of TXNIP expression by 1,25(OH)(2)D-3 was found to be dependent on the availability of glucose in the culture medium, as well as the presence of a functional glucose transport system, indicating an inter-dependence of 1,25(OH)(2)D-3 actions and glucose-sensing mechanisms. Moreover, the inhibition of de novo protein synthesis by cycloheximide reduced TXNIP half-life in 24 h, but not in 96 h-1,25(OH)(2)D-3-treated HL-60 cells, demonstrating a possible influence of 1,25(OH)(2)D-3 on TXNIP stability in long-term treatment.
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