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In the present study, we investigated the effects of mechanical compression on DRG neurons at the ultrastructural level. We examined the nanoscale changes in the surface topography of DRG neurons in response to mechanical strain, and we also evaluated neuronal apoptosis and necrosis. Using AFM, we investigated the changes in the topological details of cultured DRG neurons following the application of mechanical compression force. These forces induced increased density and size of granular structures on the cell surface. We quantitatively analyzed the membrane particle structure and showed that the granular structures on the cell membrane were correlated with the change in the mechanical compression value. In addition, mechanical compression caused remodeling of the membrane skeleton, apoptosis, and necrosis. To the best of our knowledge, this report is the first to elucidate qualitative and quantitative changes in the surface topology of DRG neurons after mechanical compression, including compression-induced cytoskeletal remodeling, and the influence of mechanical force on cell survival through membrane-skeleton changes.

In the present study, we investigated the effects of mechanical compression on neurons at the ultrastructural level. We examined the nanoscale changes in the surface topography of DRG neurons in response to mechanical strain, and we also evaluated neuronal apoptosis and necrosis. Using AFM, we investigated the changes in the topological details of cultured DRG neurons following the application of mechanical compression force. These forces induced increased density and size of granular structures on the cell surface. We quantitatively analyzed the membrane particle structure and showed that the granular structures on the cell membrane were correlated with the change in the mechanical compression value. In addition, mechanical compression caused remodeling of the membrane skeleton, apoptosis, and necrosis. To the best of our knowledge, this report is the first to elucidate qualitative and quantitative changes in the surface topology of DRG neurons after mechanical compression, including compression-induced cytoskeletal remodeling, and the influence of mechanical force on cell survival through membrane-skeleton changes. 84d34552a1