NF-κB and JAK/STAT Signaling Pathways as Crucial Regulators of Neuroinflammation and Astrocyte Modulation in Spinal Cord Injury.
Tatyana AgeevaAlbert Anatolyevich RizvanovYana MukhamedshinaPublished in: Cells (2024)
Spinal cord injury (SCI) leads to significant functional impairments below the level of the injury, and astrocytes play a crucial role in the pathophysiology of SCI. Astrocytes undergo changes and form a glial scar after SCI, which has traditionally been viewed as a barrier to axonal regeneration and functional recovery. Astrocytes activate intracellular signaling pathways, including nuclear factor κB (NF-κB) and Janus kinase-signal transducers and activators of transcription (JAK/STAT), in response to external stimuli. NF-κB and STAT3 are transcription factors that play a pivotal role in initiating gene expression related to astrogliosis. The JAK/STAT signaling pathway is essential for managing secondary damage and facilitating recovery processes post-SCI: inflammation, glial scar formation, and astrocyte survival. NF-κB activation in astrocytes leads to the production of pro-inflammatory factors by astrocytes. NF-κB and STAT3 signaling pathways are interconnected: NF-κB activation in astrocytes leads to the release of interleukin-6 (IL-6), which interacts with the IL-6 receptor and initiates STAT3 activation. By modulating astrocyte responses, these pathways offer promising avenues for enhancing recovery outcomes, illustrating the crucial need for further investigation into their mechanisms and therapeutic applications in SCI treatment.
Keyphrases
- signaling pathway
- spinal cord injury
- pi k akt
- nuclear factor
- neuropathic pain
- induced apoptosis
- epithelial mesenchymal transition
- gene expression
- lps induced
- spinal cord
- transcription factor
- oxidative stress
- cell proliferation
- toll like receptor
- type diabetes
- stem cells
- traumatic brain injury
- immune response
- dna methylation
- skeletal muscle
- lipopolysaccharide induced
- metabolic syndrome
- inflammatory response
- brain injury
- adipose tissue
- glycemic control
- subarachnoid hemorrhage