Inhibition of the JAK/STAT Pathway Protects Against α-Synuclein-Induced Neuroinflammation and Dopaminergic Neurodegeneration.
Hongwei QinJessica A BuckleyXinru LiYudong LiuThomas H FoxGordon P MearesHao YuZhaoqi YanAshley S HarmsYufeng LiDavid G StandaertEtty N BenvenistePublished in: The Journal of neuroscience : the official journal of the Society for Neuroscience (2017)
α-SYN plays a central role in the pathophysiology of PD through initiation of neuroinflammatory responses. Using an α-SYN overexpression PD model, we demonstrate a beneficial therapeutic effect of AZD1480, a specific inhibitor of JAK1/2, in suppressing neuroinflammation and neurodegeneration. Our findings document that inhibition of the JAK/STAT pathway influences both innate and adaptive immune responses by suppressing α-SYN-induced microglia and macrophage activation and CD4(+) T-cell recruitment into the CNS, ultimately suppressing neurodegeneration. These findings are the first documentation that suppression of the JAK/STAT pathway disrupts the circuitry of neuroinflammation and neurodegeneration, thus attenuating PD pathogenesis. JAK inhibitors may be a viable therapeutic option for the treatment of PD patients.
Keyphrases
- immune response
- lipopolysaccharide induced
- traumatic brain injury
- end stage renal disease
- lps induced
- high glucose
- diabetic rats
- inflammatory response
- signaling pathway
- ejection fraction
- chronic kidney disease
- cerebral ischemia
- drug induced
- cell proliferation
- peritoneal dialysis
- spinal cord injury
- neuropathic pain
- transcription factor
- dendritic cells
- electronic health record
- oxidative stress
- spinal cord
- combination therapy
- brain injury
- patient reported