Integrated stress response

The integrated stress response is a condition that can be triggered within a cell. The integrated stress response is a condition that can be triggered within a cell. The integrated stress response can be triggered within a cell due to certain conditions. These can either be extrinsic or intrinsic factors. Extrinsic factors include hypoxia, amino acid deprivation, glucose deprivation, viral infection and presence of oxidants. The main intrinsic factor is endoplasmic reticulum stress due to the accumulation of unfolded proteins. It has also been observed that the integrated stress response may trigger due to oncogene activation. The integrated stress response will either cause the expression of genes that fix the damage in the cell due to the stressful conditions, or it will cause a cascade of events leading to apoptosis, which occurs when the cell can not be brought back into homeostasis. Stress signals cause protein kinases to phosphorylate the α subunit on translation initiation factor 2 (eIF2α), resulting in the gene ATF4 being turned on, which will further affect gene expression. eIF2 consists of three subunits: eIF2α, eIF2β and eIF2γ. eIF2α contains two binding sites, one for phosphorylation and one for RNA binding. The kinases work to phosphorylate serine 51 on the α subunit, which is a reversible action. In a cell experiencing normal conditions, eIF2 aids in the initiation of mRNA translation and recognizing the AUG start codon. However, once eIF2α is phosphorylated, the complex’s activity reduces, causing reduction in translation initiation and protein synthesis, while promoting expression of the ATF4 gene. There are four known mammalian protein kinases that phosphorylate eIF2α, including PKR-like ER kinase (PERK), heme-regulated eIF2α (HRI), general control non-depressible 2 (GCN2) and double stranded RNA dependent protein kinase (PKR). PERK responds mainly to endoplasmic reticulum stress and has two modes of activation. This kinase has a unique luminal domain that plays a role in activation. The classical model of activation states that the luminal domain is normally bound to 78-kDa glucose-regulated protein (GRP78). Once there is a buildup of unfolded proteins, GRP78 dissociates from the luminal domain. This causes PERK to dimerize, leading to autophosphorylation and activation. The activated PERK kinase will then phosphorylate eIF2α, causing a cascade of events. Thus, the activation of this kinase is dependent on the aggregation of unfolded proteins in the endoplasmic reticulum. PERK has also been observed to activate in response to activity of the proto-oncogene MYC. This activation causes ATF4 expression, resulting in tumorigenesis and cellular transformation. HRI also dimerizes in order to autophosphorylate and activate. This activation is dependent on the presence of heme. HRI has two domains that heme may bind to, including one on the N-terminus and one on the kinase insertion domain. The presence of heme causes a disulfide bond to form between the monomers of HRI, resulting in the structure of an inactive dimer. However, when heme is absent, HRI monomers form an active dimer through non-covalent interactions. Therefore, the activation of this kinase is dependent on heme deficiency. HRI activation can also occur due to other stressors such as heat shock, osmotic stress and proteasome inhibition. Activation of HRI in response to these stressors does not depend on heme, but rather relies on the help of two heat shock proteins (HSP90 and HSP70). HRI is mainly found in the precursors of red blood cells, and has been observed to increase during erythropoiesis. GCN2 is activated as a result of amino acid deprivation. The mechanisms regarding this activation are still being researched, however, one mechanism has been studied in yeast. It was observed that GCN2 binds to uncharged/deacylated tRNA which causes a conformational change, resulting in dimerization. Dimerization then causes autophosphorylation and activation. Other stressors have also been reported to activate GCN2. GCN2 activation was observed in glucose deprived tumor cells, although it was suggested that it was an indirect effect due to cells using amino acids as an alternate energy source. In mouse embryonic fibroblast cells and human keratinocytes, GCN2 was activated due to UV light exposure. The pathways for this activation require further research, although multiple models have been proposed, including crosslinking between GCN2 and tRNA. PKR activation is mainly dependent on the presence of double-stranded RNA during a viral infection. dsRNA causes PKR to form dimers, resulting in autophosphorylation and activation. Once activated, PKR will phosphorylate eIF2α which causes a cascade of events that result in viral and host protein synthesis being inhibited. Other stressors that cause the activation of PKR include oxidative stress, endoplasmic reticulum stress, growth factor deprivation and bacterial infection. Caspase activity early on in apoptosis has also been observed to trigger activation of PKR. However, these stressors differ in that they activate PKR without using dsRNA. When a cell is subjected to stressful conditions, the ATF4 gene is expressed. The ATF4 transcription factor has the ability to form dimers with many different proteins that influence gene expression and cell fate. ATF4 binds to C/EBP‐ATF response element (CARE) sequences which work together to increase the transcription of stress-responsive genes. However, when undergoing amino acid starvation, the sequences will act as amino acid response elements instead.