Protein kinase R1 (PKR1) is a cellular enzyme that plays a critical role in the regulation of various biological processes. As a kinase, its primary function involves the phosphorylation of specific substrates, which can alter their activity and stability, thus impacting signal transduction pathways within the cell. The exact biological functions of PKR1 are subject to ongoing research, but it is understood that kinases like PKR1 are often pivotal in cellular responses to environmental stresses and may be involved in the intricate network of signaling that maintains cellular homeostasis. The expression of PKR1 is not static; it can be induced under certain conditions, particularly in response to stimuli that the cell interprets as signaling the need for a defensive or adaptive response.
Several chemical compounds have been identified that can potentially induce the expression of PKR1. These activators are diverse in structure and origin but are united by their capacity to elicit a cellular response that includes the upregulation of PKR1. For instance, compounds like sodium salicylate can increase PKR1 expression through the inhibition of specific signaling pathways, prompting the cell to enhance its readiness against stressors. Actinomycin D and tunicamycin are known to induce cellular stress by interfering with fundamental processes such as DNA transcription and protein folding, respectively, which can lead to an upsurge in PKR1 expression as part of the cell's effort to cope with these stressors. Other compounds, like thapsigargin and chloroquine, disrupt intracellular calcium stores and lysosomal function, respectively, necessitating the cell to activate compensatory mechanisms which include the increased expression of PKR1. Such activators highlight the cell's reliance on PKR1 as part of a broader adaptative response to maintain cellular function and integrity in the face of diverse challenges. The interactions between PKR1 and these chemical activators underscore the intricate web of cellular signaling and the adaptability of the cell's molecular machinery. Understanding these interactions further clarifies the role of PKR1 in cellular physiology and highlights the dynamic nature of its expression in response to the cellular environment.
| Product Name | CAS # | Catalog # | QUANTITY | Price | Citations | RATING |
|---|---|---|---|---|---|---|
Sodium Salicylate | 54-21-7 | sc-3520 sc-3520A sc-3520B sc-3520C | 1 g 25 g 500 g 1 kg | $10.00 $25.00 $80.00 $136.00 | 8 | |
Sodium Salicylate can lead to an increase in PKR expression by inhibiting the NF-kB pathway, which may cause a compensatory upsurge in antiviral proteins, including PKR, to maintain immune readiness. | ||||||
Actinomycin D | 50-76-0 | sc-200906 sc-200906A sc-200906B sc-200906C sc-200906D | 5 mg 25 mg 100 mg 1 g 10 g | $73.00 $238.00 $717.00 $2522.00 $21420.00 | 53 | |
Actinomycin D, known as an inducer of cellular stress, can provoke an increase in PKR expression as cells activate various stress response pathways to mitigate damage. | ||||||
Tunicamycin | 11089-65-9 | sc-3506A sc-3506 | 5 mg 10 mg | $169.00 $299.00 | 66 | |
Tunicamycin initiates endoplasmic reticulum stress, which can lead to a robust upregulation of PKR as part of the unfolded protein response, a cellular protective measure. | ||||||
Thapsigargin | 67526-95-8 | sc-24017 sc-24017A | 1 mg 5 mg | $94.00 $349.00 | 114 | |
Thapsigargin, by disrupting calcium homeostasis within the endoplasmic reticulum, can precipitate a sharp increase in PKR expression due to the activation of stress response pathways. | ||||||
LY 294002 | 154447-36-6 | sc-201426 sc-201426A | 5 mg 25 mg | $121.00 $392.00 | 148 | |
LY 294002, by inhibiting PI3K, can dismantle a key survival signaling pathway, which can subsequently lead to the upregulation of PKR as the cell mounts a stress-induced defensive response. | ||||||
Retinoic Acid, all trans | 302-79-4 | sc-200898 sc-200898A sc-200898B sc-200898C | 500 mg 5 g 10 g 100 g | $65.00 $319.00 $575.00 $998.00 | 28 | |
Retinoic Acid can upregulate gene expression tied to antiviral defense, including the synthesis of PKR, as part of the cell's effort to prepare against viral infection. | ||||||
Chloroquine | 54-05-7 | sc-507304 | 250 mg | $68.00 | 2 | |
Chloroquine, through its role in hindering lysosomal acidification, can lead to an increase in PKR expression as part of the cell's attempt to compensate for disrupted cellular homeostasis. | ||||||
Hydrogen Peroxide | 7722-84-1 | sc-203336 sc-203336A sc-203336B | 100 ml 500 ml 3.8 L | $30.00 $60.00 $93.00 | 27 | |
Hydrogen peroxide, as an inducer of oxidative stress, can lead to a heightened synthesis of PKR due to its role in combating oxidative damage within the cell. | ||||||