Monounsaturated Fatty Acids Prevent the Deleterious Effects of Palmitate and High Glucose on Human Pancreatic β-Cell Turnover and Function
TL;DR: In human islets, the saturated palmitic acid and elevated glucose concentration induce beta-cell apoptosis, decreasebeta-cell proliferation, and impair beta- cell function, which can be prevented by monounsaturated fatty acids.
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Abstract: Glucotoxicity and lipotoxicity contribute to the impaired β-cell function observed in type 2 diabetes. Here we examine the effect of saturated and monounsaturated fatty acids at different glucose concentrations on human β-cell turnover and secretory function. Exposure of cultured human islets to saturated fatty acid and/or to an elevated glucose concentration for 4 days increased β-cell DNA fragmentation and decreased β-cell proliferation. In contrast, the monounsaturated palmitoleic acid or oleic acid did not affect DNA fragmentation and induced β-cell proliferation. Moreover, each monounsaturated fatty acid prevented the deleterious effects of both palmitic acid and high glucose concentration. The cell-permeable ceramide analogue C 2 -ceramide mimicked both the palmitic acid-induced β-cell apoptosis and decrease in proliferation. Furthermore, the ceramide synthetase inhibitor fumonisin B1 blocked the deleterious effects of palmitic acid on β-cell turnover. In addition, palmitic acid decreased Bcl-2 expression and induced release of cytochrome c from the mitochondria into the cytosol, which was prevented by fumonisin B1 and by oleic acid. Finally, each monounsaturated fatty acid improved β-cell secretory function that was reduced by palmitic acid and by high glucose. Thus, in human islets, the saturated palmitic acid and elevated glucose concentration induce β-cell apoptosis, decrease β-cell proliferation, and impair β-cell function, which can be prevented by monounsaturated fatty acids. The deleterious effect of palmitic acid is mediated via formation of ceramide and activation of the apoptotic mitochondrial pathway, whereas Bcl-2 may contribute to the protective effect of monounsaturated fatty acids.
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The mammalian STE20-like kinase 1 (MST1) is a substrate for the apoptosis inhibiting protein kinase CK2.
TL;DR: Serine 320 of the MST1 protein is a novel phosphorylation site for the anti-apoptotic protein kinase CK2, and binding of these two kinases in the cytosol and in the nucleus opens the door to the phosphorylated of a variety of new substrates.
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•Dissertation
The effect of single nucleotide polymorphisms and metabolic substrates on the cellular distribution of mammalian BK channels
Bernadette Ayokunumi Adeyileka-Tracz
- 01 Sep 2017
TL;DR: It was shown that exposure to metabolic substrates glucose, palmitate and oleate modulated SNP-mimetic cellular distribution and could invert the 'C56 palmitoylation pattern', indicating that there is interplay between the metabolic status of the cell and the amino-acid composition of the channel via palMIToylation.
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Structure-activity relationships influencing lipid-induced changes in eIF2α phosphorylation and cell viability in BRIN-BD11 cells.
Shalinee Dhayal,Noel G. Morgan +1 more
TL;DR: Both physical properties and specific signalling events may regulate fatty acid responses in β‐cells and a wide range of unsaturated free fatty acids and their methyl‐esters elicit cytoprotection and relief of protein kinase RNA‐like endoplasmic reticulum kinase‐dependent ER stress.
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Monounsaturated fatty acids protect against palmitate-induced lipoapoptosis in human umbilical vein endothelial cells.
Dustin M. Lee,Kyle J. Sevits,Micah L. Battson,Yuren Wei,Kimberly Cox-York,Christopher L. Gentile +5 more
TL;DR: Monounsaturated fatty acids confer protection against the cytotoxic effects of palmitate in vascular endothelial cells; andPalmitate-mediated damage, as well as monouns saturated-mediated protection, are due in part to inactivation and activation, respectively, of the metabolic regulator AMPK.
Prolactin and oleic acid synergistically stimulate β-cell proliferation and growth in rat islets.
TL;DR: The novel observation that prolactin and oleic acid synergistically stimulate islet cell proliferation and islet growth in rat islets is reported, and methyl olei acid, a non-metabolizable analog of oleoic acid, also shows synergy with Prolactin.
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