Keratinocyte-derived extracellular vesicles in painful diabetic neuropathy

• Published in: Neurobiology of pain 2025-01, Vol.17, p.100176, Article 100176
• Main Authors: Coy-Dibley, James, Jayaraj, Nirupa D., Ren, Dongjun, Pacifico, Paola, Belmadani, Abdelhak, Wang, Yi-Zhi, Gebis, Kamil K., Savas, Jeffrey N., Paller, Amy S., Miller, Richard J., Menichella, Daniela M.
• Format: Article
• Language: English
• Subjects: Alix; DRG neuron; Extracellular vesicle; Keratinocyte; Original Research; Painful diabetic neuropathy; Peripheral pain; Retrograde transport; Size exclusion chromatography; Skin; Small-fiber neuropathy; Tunable resistive pulse sensing (TRPS)
• ISSN: 2452-073X; 2452-073X
• DOI: 10.1016/j.ynpai.2024.100176

•Keratinocyte-derived extracellular vesicles are isolated by size exclusion chromatography.•Keratinocyte-derived extracellular vesicles alter their molecular cargo in a mouse model of Painful Diabetic Neuropathy.•Epidermal extracellular vesicles are retrogradely trafficked into the DRG neuron cell bodies in mice. Painful diabetic neuropathy (PDN) is a challenging complication of diabetes with patients experiencing a painful and burning sensation in their extremities. Existing treatments provide limited relief without addressing the underlying mechanisms of the disease. PDN involves the gradual degeneration of nerve fibers in the skin. Keratinocytes, the most abundant epidermal cell type, are closely positioned to cutaneous nerve terminals, suggesting the possibility of bi-directional communication. Extracellular vesicles are lipid-bilayer encapsulated nanovesicles released from many cell types that mediate cell to cell communication. The role of keratinocyte-derived extracellular vesicles (KDEVs) in influencing signaling between the skin and cutaneous nerve terminals and their contribution to the genesis of PDN has not been explored. In this study, we characterized KDEVs in a well-established high-fat diet mouse model of PDN using primary adult mouse keratinocyte cultures. We obtained highly enriched KDEVs through size-exclusion chromatography and then analyzed their molecular cargo using proteomic analysis and small RNA sequencing. We found significant differences in the protein and microRNA content of high-fat diet KDEVs compared to KDEVs obtained from control mice on a regular diet, including pathways involved in axon guidance and synaptic transmission. Additionally, using an in vivo conditional extracellular vesicle reporter mouse model, we demonstrated that epidermal-originating GFP-tagged KDEVs are retrogradely trafficked into the dorsal root ganglion (DRG) neuron cell bodies. This study presents the first comprehensive isolation and molecular characterization of the KDEV protein and microRNA cargo in RD and HFD mice. Our findings suggest a potential novel communication pathway between keratinocytes and DRG neurons in the skin, which could have implications for PDN.