{"id":16695,"date":"2021-04-20T12:32:00","date_gmt":"2021-04-20T10:32:00","guid":{"rendered":"https:\/\/idibell.cat\/es\/?post_type=agenda&p=16695"},"modified":"2021-04-20T12:41:03","modified_gmt":"2021-04-20T10:41:03","slug":"idibellseminars-immune-synaptopathies-when-the-immune-system-affects-synaptic-function","status":"publish","type":"agenda","link":"https:\/\/idibell.cat\/es\/agenda\/idibellseminars-immune-synaptopathies-when-the-immune-system-affects-synaptic-function\/","title":{"rendered":"#IDIBELLseminars: Immune-synaptopathies: When the immune system affects synaptic function"},"content":{"rendered":"

Michela Matteoli<\/strong>
\nCNR Institute of Neuroscience and Humanitas University, Milano<\/p>\n

The synapse is the core component of the nervous system and synapse formation is the critical step in the assembly of neuronal circuits. The assembly and maturation of synapses requires the contribution of secreted and membrane-associated proteins, with neuronal activity playing crucial roles in regulating synaptic strength, neuronal membrane properties, and neural circuit refinement. The molecular mechanisms of synapse assembly and refinement have been so far largely examined on a gene-by-gene basis and with a perspective fully centered on neuronal cells. However, in the last years, the involvement of non-neuronal cells has emerged. Among these, microglia, the resident immune cells of the central nervous system, have been shown to play a key role in synapse formation and elimination. Contacts of microglia with dendrites in the somatosensory cortex were found to induce filopodia and dendritic spines via Ca2+ and actin-dependent processes, while microglia-derived BDNF was shown to promote learning-dependent synapse formation. Microglia is also recognized to have a central role in the widespread elimination (or pruning) of exuberant synaptic connections during development. Clarifying the processes by which microglia control synapse homeostasis is essential to advance our current understanding of brain functions. Clear answers to these questions will have important implications for our understanding of brain diseases, as the fact that many psychiatric and neurological disorders are synaptopathies (i.e. diseases of the synapse) is now widely recognized.<\/p>\n

In the last years, my group has identified TREM2, an innate immune receptor with phagocytic and anti-inflammatory properties expressed in brain exclusively by microglia, as essential for microglia-mediated synaptic refinement during the early stages of brain development. The talk will describe the role of TREM2 in synapse elimination and introduce the molecular actors involved. I will also describe additional pathways by which the immune system may affect the formation and homeostasis of synaptic contacts.<\/p>\n

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