TPL2 kinase activity regulates microglial inflammatory responses and promotes neurodegeneration in tauopathy mice
Ontology highlight
ABSTRACT:
PROVIDER: PRJNA804717 | ENA |
REPOSITORIES: ENA
Dataset's files
| Action | DRS | |||
|---|---|---|---|---|
| SRR17970529.fastq.gz | Fastqsanger.gz | |||
| SRR17970530.fastq.gz | Fastqsanger.gz | |||
| SRR17970531.fastq.gz | Fastqsanger.gz | |||
| SRR17970532.fastq.gz | Fastqsanger.gz | |||
| SRR17970533.fastq.gz | Fastqsanger.gz |
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Project description:TPL2 (MAP3K8) is a central signaling node in the inflammatory response of peripheral immune cells. We find that TPL2 kinase activity modulates microglial cytokine release and is required for microglia-mediated neuron death in vitro. In acute in vivo neuroinflammation settings, TPL2 kinase activity regulates cytokine levels and activation states of microglia. In a tauopathy model of chronic neurodegeneration, loss of TPL2 kinase activity reduces neuroinflammation and rescues synapse loss, brain volume loss, and behavioral deficits. Single-cell RNAseq analysis indicates protection in the tauopathy model was associated with reductions in activated microglia subpopulations as well as infiltrating peripheral immune cells. Overall, using various models, we find that TPL2 kinase activity promotes multiple harmful consequences of microglial activation in the brain including cytokine release, iNOS induction, astrocyte activation, and immune cell infiltration. Consequently, inhibiting TPL2 kinase activity could represent a potential therapeutic strategy in neurodegenerative conditions.
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