MiR-7a-Klf4 axis as a regulator and therapeutic target of neuroinflammation and ferroptosis in Alzheimer's disease.

ABSTRACT: Neuroinflammation and ferroptosis significantly contribute to neuronal death in Alzheimer's disease (AD) and other neurodegenerative disorders. MicroRNAs (miRNAs) are crucial regulators of these pathological processes. We employed transcriptomic analysis in an APP/PSEN1 Tg AD mouse model to identify dysregulated miRNAs and construct a miRNA-mRNA pathway network. We discovered increased miR-7a expression in the AD brain, targeting Krüppel-like factor 4 (Klf4), a transcriptional factor implicated in amyloid-β (Aβ) oligomer-induced neuroinflammation and RSL3-induced neuronal ferroptosis. Elevated Klf4 levels in AD mice brains suggest its involvement in AD pathology. The miR-7a mediated silencing of Klf4 alleviates neuroinflammation by modulating NF-κB, iNOS, and NLRP3 pathways, and inhibition

SUBMITTER: Ramesh M 

PROVIDER: S-EPMC12429957 | biostudies-literature | 2025 Jul

REPOSITORIES: biostudies-literature