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Zinc modulates several transcription-factor regulated pathways in mouse skeletal muscle cells


Vahidi Ferdowsi, P and Ng, R and Adulcikas, J and Sohal, SS and Myers, S, Zinc modulates several transcription-factor regulated pathways in mouse skeletal muscle cells, Molecules, 25, (21) Article 5098. ISSN 1420-3049 (2020) [Refereed Article]


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© 2020 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license

DOI: doi:10.3390/molecules25215098


Zinc is an essential metal ion involved in many biological processes. Studies have shown that zinc can activate several molecules in the insulin signalling pathway and the concomitant uptake of glucose in skeletal muscle cells. However, there is limited information on other potential pathways that zinc can activate in skeletal muscle. Accordingly, this study aimed to identify other zinc-activating pathways in skeletal muscle cells to further delineate the role of this metal ion in cellular processes. Mouse C2C12 skeletal muscle cells were treated with insulin (10 nM), zinc (20 ĶM), and the zinc chelator TPEN (various concentrations) over 60 min. Western blots were performed for the zinc-activation of pAkt, pErk, and pCreb. A Cignal 45-Reporter Array that targets 45 signalling pathways was utilised to test the ability of zinc to activate pathways that have not yet been described. Zinc and insulin activated pAkt over 60 min as expected. Moreover, the treatment of C2C12 skeletal muscle cells with TPEN reduced the ability of zinc to activate pAkt and pErk. Zinc also activated several associated novel transcription factor pathways including Nrf1/Nrf2, ATF6, CREB, EGR1, STAT1, AP-1, PPAR, and TCF/LEF, and pCREB protein over 120 min of zinc treatment. These studies have shown that zincís activity extends beyond that of insulin signalling and plays a role in modulating novel transcription factor activated pathways. Further studies to determine the exact role of zinc in the activation of transcription factor pathways will provide novel insights into this metal ion actions.

Item Details

Item Type:Refereed Article
Keywords:zinc, skeletal muscle, transcription factors, cell signalling, insulin
Research Division:Biological Sciences
Research Group:Biochemistry and cell biology
Research Field:Analytical biochemistry
Objective Division:Health
Objective Group:Clinical health
Objective Field:Prevention of human diseases and conditions
UTAS Author:Vahidi Ferdowsi, P (Ms Parisa Vahidi Ferdowsi)
UTAS Author:Ng, R (Miss Rachel Ng)
UTAS Author:Adulcikas, J (Mr John Adulcikas)
UTAS Author:Sohal, SS (Dr Sukhwinder Sohal)
UTAS Author:Myers, S (Dr Stephen Myers)
ID Code:141813
Year Published:2020
Web of Science® Times Cited:5
Deposited By:Health Sciences
Deposited On:2020-11-24
Last Modified:2022-08-19
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