Osteoclast-derived extracellular vesicles are implicated in sensory neurons sprouting through the activation of epidermal growth factor signaling

• Published in: Cell & bioscience 2022-08, Vol.12 (1), p.1-127, Article 127
• Main Authors: Neto, Estrela, Leitão, Luís, Mateus, José C, Sousa, Daniela M, Alves, Cecília J, Aroso, Miguel, Monteiro, Ana C, Conceição, Francisco, Oreffo, Richard O. C, West, Jonathan, Aguiar, Paulo, Lamghari, Meriem
• Format: Article
• Language: English
• Subjects: Axon guidance; Bone pain; Brain-derived neurotrophic factor; Cartilage; Epidermal growth factor; Epidermal growth factor receptor (EGFR/ErbB2) signaling; ErbB-2 protein; Extracellular vesicles; Homeostasis; Innervation; Kinases; Microenvironments; Nervous system; Neuronal electrophysiology; Neurons; Osteoclast secretome; Osteoclasts; Pattern formation; Phosphorylation; Protein kinase C; Sensory neurons; Sensory neurons sprouting; Stem cells
• ISSN: 2045-3701; 2045-3701
• DOI: 10.1186/s13578-022-00864-w

Different pathologies, affecting the skeletal system, were reported to display altered bone and/or cartilage innervation profiles leading to the deregulation of the tissue homeostasis. The patterning of peripheral innervation is achieved through the tissue-specific expression of attractive or repulsive axonal guidance cues in specific space and time frames. During the last decade, emerging findings attributed to the extracellular vesicles (EV) trading a central role in peripheral tissue innervation. However, to date, the contribution of EV in controlling bone innervation is totally unknown. Here we show that sensory neurons outgrowth induced by the bone resorbing cells--osteoclasts--is promoted by osteoclast-derived EV. The EV induced axonal growth is achieved by targeting epidermal growth factor receptor (EGFR)/ErbB2 signaling/protein kinase C phosphorylation in sensory neurons. In addition, our data also indicate that osteoclasts promote sensory neurons electrophysiological activity reflecting a possible pathway in nerve sensitization in the bone microenvironment, however this effect is EV independent. Overall, these results identify a new mechanism of sensory bone innervation regulation and shed the light on the role of osteoclast-derived EV in shaping/guiding bone sensory innervation. These findings provide opportunities for exploitation of osteoclast-derived EV based strategies to prevent and/or mitigate pathological uncontrolled bone innervation.