| |
[摘要]：A growing body of research suggests that fructose 1,6-bisphosphatase (FBPase) might be involved in regulation of cell mortality/survival. However, the precise role of FBPase in the process remains unknown. Here, we show for the first time that in HL-1 cardiomyocytes, inhibition of glycogen synthase kinase-3 results in translocation of FBPase to mitochondria. In vitro experiments demonstrate that FBPase reduces the rate of calcium-induced mitochondrial swelling, affects ATP synthesis and interacts with mitochondrial proteins involved in regulation of volume and energy homeostasis. We suggest that FBPase might be engaged in a regulation of cell survival by influencing mitochondrial function. Structured summary of protein interactions: FBPase physically interacts with VDAC2, Vdac3, ATP synthase subunit beta, Slc25a5, ATP synthase subunit alpha, Histone cluster 1, H1d, Histone H2A, Histone H4 and Histone H3 by affinity chromatography technology (View interaction) FBPase physically interacts with ATP synthase subunit beta, ATP synthase subunit alpha, ADP/ATP translocase 1, ADP/ATP translocase 2 and VDAC2 by cross-linking study (View interaction) (C) 2011 Federation of European Biochemical Societies. Published by Elsevier B.V. All rights reserved. |
|
