After reperfusion following brain
ischemia, there is inhibition of neuron protein synthesis due to phosphorylation of eIF2α. There is colocalization between phosphorylated eIF2α and
cytosolic
cytochrome c, which is released from
mitochondria in
apoptosis. Phosphorylated Eif2-alpha appeared before cytochrome c release, suggesting that phosphorylation of eIF2α triggers cytochrome c release during apoptotic cell death. Mice
heterozygous for the S51A
mutation become obese and
diabetic on a high-fat diet.
Glucose intolerance resulted from reduced
insulin secretion, defective transport of proinsulin, and a reduced number of insulin granules in
beta cells. Hence proper functioning of eIF2α appears essential for preventing diet-induced
type II diabetes. ==Dephosphorylation inhibitors==