Research focus
Craniofacial neuropathic pain
Chronic pain in the craniofacial region (“trigeminal chronic pain”) is a common ̽ѡ problem that is difficult to treat; currently available remedies are compromised by side effects and offer only partial pain relief. Like other chronic pain syndromes, trigeminal pain is a complex genetic trait; analyses of human and animal models indicate that ~50% of the inter-individual differences in neuropathic pain levels are genetically controlled.
Our objective is to identify genetic factors affecting trigeminal pain syndromes, with emphasis on orofacial conditions. This may open new ways of understanding the functional relationship between nociceptors and their surrounding tissue, and be helpful in search for better therapies against dental pain.
The role of the peripheral innervation in the formation of teeth
From an evolutionary standpoint, teeth are essential for both feeding and fending. Teeth develop through very complex mechanisms through coordinated actions between neural crest stem cells and the ectoderm of a brachial arch. They consist of a hard matrix and matrix producing cells (odontoblasts), pulp cells, vessels and a protective sensory innervation with adjacent glia. Available evidence has suggested that the developmental growth and establishment of sensory pain-transmitting nerve terminals in relation to teeth are controlled by local molecular signals. We address the role of a sensory nerve as a provider of tooth stem cells during the development, adulthood and in regeneration. We use genetic tracing with multicolour reporters, transgenic mice with cell type-specific modifications in signaling, microsurgery and grafting, in vitro cell cultures and 3D-imaging.
