Cardiomyocyte protein O-GlcNAcylation is regulated by GFAT1 not GFAT2.
Nabeebaccus, Adam A
Santos, Celio Xc
Shah, Ajay M
Biochem Biophys Res Commun
MetadataShow full item record
Nabeebaccus, A. A., Verma, S., Zoccarato, A., Emanuelli, G., Santos, C. X., Streckfuss-Bömeke, K., & Shah, A. M. (2021). Cardiomyocyte protein O-GlcNAcylation is regulated by GFAT1 not GFAT2.. Biochem Biophys Res Commun, 583 121-127. https://doi.org/10.1016/j.bbrc.2021.10.056
In response to cardiac injury, increased activity of the hexosamine biosynthesis pathway (HBP) is linked with cytoprotective as well as adverse effects depending on the type and duration of injury. Glutamine-fructose amidotransferase (GFAT; gene name gfpt) is the rate-limiting enzyme that controls flux through HBP. Two protein isoforms exist in the heart called GFAT1 and GFAT2. There are conflicting data on the relative importance of GFAT1 and GFAT2 during stress-induced HBP responses in the heart. Using neonatal rat cardiac cell preparations, targeted knockdown of GFPT1 and GFPT2 were performed and HBP activity measured. Immunostaining with specific GFAT1 and GFAT2 antibodies was undertaken in neonatal rat cardiac preparations and murine cardiac tissues to characterise cell-specific expression. Publicly available human heart single cell sequencing data was interrogated to determine cell-type expression. Western blots for GFAT isoform protein expression were performed in human cardiomyocytes derived from induced pluripotent stem cells (iPSCs). GFPT1 but not GFPT2 knockdown resulted in a loss of stress-induced protein O-GlcNAcylation in neonatal cardiac cell preparations indicating reduced HBP activity. In rodent cells and tissue, immunostaining for GFAT1 identified expression in both cardiac myocytes and fibroblasts whereas immunostaining for GFAT2 was only identified in fibroblasts. Further corroboration of findings in human heart cells identified an enrichment of GFPT2 gene expression in cardiac fibroblasts but not ventricular myocytes whereas GFPT1 was expressed in both myocytes and fibroblasts. In human iPSC-derived cardiomyocytes, only GFAT1 protein was expressed with an absence of GFAT2. In conclusion, these results indicate that GFAT1 is the primary cardiomyocyte isoform and GFAT2 is only present in cardiac fibroblasts. Cell-specific isoform expression may have differing effects on cell function and should be considered when studying HBP and GFAT functions in the heart.
GFAT1, GFAT2, GFPT1, GFPT2, Hexosamine biosynthesis pathway, O-GlcNAc, Animals, Fibroblasts, Glutamine-Fructose-6-Phosphate Transaminase (Isomerizing), Hexosamines, Induced Pluripotent Stem Cells, Mice, Myocardium, Myocytes, Cardiac, Protein Isoforms, Rats, Sprague-Dawley
External DOI: https://doi.org/10.1016/j.bbrc.2021.10.056
This record's URL: https://www.repository.cam.ac.uk/handle/1810/332697
Attribution 4.0 International
Licence URL: https://creativecommons.org/licenses/by/4.0/