Inflammation: A New Look at an Old Problem.
Evgenii GusevYulia ZhuravlevaPublished in: International journal of molecular sciences (2022)
Pro-inflammatory stress is inherent in any cells that are subject to damage or threat of damage. It is defined by a number of universal components, including oxidative stress, cellular response to DNA damage, unfolded protein response to mitochondrial and endoplasmic reticulum stress, changes in autophagy, inflammasome formation, non-coding RNA response, formation of an inducible network of signaling pathways, and epigenetic changes. The presence of an inducible receptor and secretory phenotype in many cells is the cause of tissue pro-inflammatory stress. The key phenomenon determining the occurrence of a classical inflammatory focus is the microvascular inflammatory response (exudation, leukocyte migration to the alteration zone). This same reaction at the systemic level leads to the development of life-critical systemic inflammation. From this standpoint, we can characterize the common mechanisms of pathologies that differ in their clinical appearance. The division of inflammation into alternative variants has deep evolutionary roots. Evolutionary aspects of inflammation are also described in the review. The aim of the review is to provide theoretical arguments for the need for an up-to-date theory of the relationship between key human pathological processes based on the integrative role of the molecular mechanisms of cellular and tissue pro-inflammatory stress.
Keyphrases
- oxidative stress
- induced apoptosis
- endoplasmic reticulum stress
- dna damage
- diabetic rats
- ischemia reperfusion injury
- inflammatory response
- signaling pathway
- gene expression
- dna methylation
- endothelial cells
- stress induced
- heat shock
- binding protein
- epithelial mesenchymal transition
- cell death
- protein protein
- nucleic acid
- immune response