2010
DOI: 10.4161/isl.2.1.10456
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Stress hypERactivation in the β-cell

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Cited by 46 publications
(33 citation statements)
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References 114 publications
(141 reference statements)
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“…These cells are more susceptible to endoplasmic reticulum stress because of their high secreting activities and low antioxidant capacities [32] , which is in agreement to our findings. However, others reported that patulin had hyperglycemic effect due to increased glycogen phosphorylase, glucose 6-phosphatase and fructose 1, 6 diphosphatase activities as well as decreased glycolytic enzymes as hexokinase and aldolase [33] .…”
Section: Discussionsupporting
confidence: 92%
“…These cells are more susceptible to endoplasmic reticulum stress because of their high secreting activities and low antioxidant capacities [32] , which is in agreement to our findings. However, others reported that patulin had hyperglycemic effect due to increased glycogen phosphorylase, glucose 6-phosphatase and fructose 1, 6 diphosphatase activities as well as decreased glycolytic enzymes as hexokinase and aldolase [33] .…”
Section: Discussionsupporting
confidence: 92%
“…One of the events inducing differences in PTM in b-cells is disruption of homeostasis of the endoplasmic reticulum (ER) in b-cells leads to cell death and contributes to T1D pathogenesis (30)(31)(32). Upon ER stress, proteins are misfolded or modified, changing the structure of the protein.…”
Section: Discussionmentioning
confidence: 99%
“…Role of Cdc37-Hsp90-mediated IRE1 Regulation in Insulin Production and Secretion-Insulin synthesis in pancreatic ␤-cells requires a balanced ER stress response to maintain ER flux (19,20). An increase in IRE1␣ activity is associated with insulin biosynthesis, whereas sustained IRE1␣ activity or Advmediated expression of XBP1s decreased insulin expression in ␤-cells (21,22).…”
Section: Cdc37 Regulates Ire1␣ Activity Through Direct Interaction Wimentioning
confidence: 99%