Regulation of the Nuclear–Cytoplasmic Traffic of Class IIa Histone Deacethylases in Rat Soleus Muscle at the Early Stage of Gravitational Unloading
- Authors: Vilchinskaya N.A.1, Turtikova O.V.1, Shenkman B.S.1
-
Affiliations:
- Institute of Biomedical Problems
- Issue: Vol 12, No 1 (2018)
- Pages: 27-32
- Section: Articles
- URL: https://journal-vniispk.ru/1990-7478/article/view/213285
- DOI: https://doi.org/10.1134/S1990747818010117
- ID: 213285
Cite item
Abstract
The negative regulation of expression of genes involved in various metabolic pathways in a skeletal muscle is the main function of histone deacetylases 4 and 5 (HDAC4/HDAC5). HDAC4 and HDAC5 seem to be the targets of the AMP-activated protein kinase (AMPK). Earlier, an essential decrease in the level of Thr172-phosphorylated-AMPK in a rat soleus muscle at the first day of gravitational unloading was shown. Possibility of a protein kinase D (PKD) to phosphorylate histone deacetylases 4/5 has been shown, too. We supposed that under the conditions of gravitational unloading, alterations in AMPK phosphorylation level can affect regulation of nuclear-cytoplasmic traffic of class II histone deacetylases and of various skeletal muscle genes expression. To verify the hypothesis, we used administration of an AMPK activator, AICAR, before and during a day-long hindlimb suspension. It was shown that at an early stage of gravitational unloading, HDAC4 is not a PKD target, and its nuclear import is realized due to decrease in AMPK activity. We were the first to show reciprocal relations between AMPK and PKD in a skeletal muscle at early gravitational unloading.
Keywords
About the authors
N. A. Vilchinskaya
Institute of Biomedical Problems
Author for correspondence.
Email: Vilchinskaya2008@rambler.ru
Russian Federation, Moscow, 123007
O. V. Turtikova
Institute of Biomedical Problems
Email: Vilchinskaya2008@rambler.ru
Russian Federation, Moscow, 123007
B. S. Shenkman
Institute of Biomedical Problems
Email: Vilchinskaya2008@rambler.ru
Russian Federation, Moscow, 123007
Supplementary files
