Keratinocytes drive psoriasis inflammation through bidirectional epithelial-immune crosstalkSkin cells play a key role in driving psoriasis inflammation

Psoriasis is a chronic immune-mediated inflammatory skin disease historically viewed as a disorder of keratinocyte hyperplasia, with subsequent recognition of central immune cell involvement. However, accumulating multi-omics and functional genomic evidence has reshaped this paradigm, positioning keratinocytes not merely as passive targets of immune attack but as active participants within a bidirectional epithelial-immune network that drives inflammatory initiation, maintenance, and amplification. This critical narrative review synthesizes the molecular mechanisms by which keratinocytes integrate genetic susceptibility, environmental triggers, metabolic reprogramming, and cell death programs to modulate psoriatic inflammation. We examine interleukin (IL)-1/IL-36 cytokines, the dual function of the antimicrobial peptide LL-37, danger signal release and dendritic cell recruitment, chemokine networks and exosome-mediated communication, the neuropeptide-keratinocyte axis, carbohydrate and lipid metabolic abnormalities, mitochondrial dysfunction and reactive oxygen species (ROS)-mediated feedback, epidermal barrier defects and microbiome dysregulation, diagnostic biomarkers, and therapeutic innovations. We further critically evaluate controversies, conceptual challenges, research gaps, and future directions. A keratinocyte-centric framework—situated within the broader context of epithelial-immune reciprocity—advances understanding of psoriasis pathogenesis and informs precision therapies targeting the barrier-immune axis.