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Regional, Layer, and Cell-Type-Specific Connectivity of the Mouse Default Mode Network

The evolutionarily conserved default mode network (DMN) is a distributed set of brain regions coactivated during resting states that is vulnerable to brain disorders. How disease affects the DMN is unknown, but detailed anatomical descriptions could provide clues. Mice offer an opportunity to invest...

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Detalles Bibliográficos
Autores principales: Whitesell, Jennifer D., Liska, Adam, Coletta, Ludovico, Hirokawa, Karla E., Bohn, Phillip, Williford, Ali, Groblewski, Peter A., Graddis, Nile, Kuan, Leonard, Knox, Joseph E., Ho, Anh, Wakeman, Wayne, Nicovich, Philip R., Nguyen, Thuc Nghi, van Velthoven, Cindy T.J., Garren, Emma, Fong, Olivia, Naeemi, Maitham, Henry, Alex M., Dee, Nick, Smith, Kimberly A., Levi, Boaz, Feng, David, Ng, Lydia, Tasic, Bosiljka, Zeng, Hongkui, Mihalas, Stefan, Gozzi, Alessandro, Harris, Julie A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Cell Press 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8150331/
https://www.ncbi.nlm.nih.gov/pubmed/33290731
http://dx.doi.org/10.1016/j.neuron.2020.11.011
Descripción
Sumario:The evolutionarily conserved default mode network (DMN) is a distributed set of brain regions coactivated during resting states that is vulnerable to brain disorders. How disease affects the DMN is unknown, but detailed anatomical descriptions could provide clues. Mice offer an opportunity to investigate structural connectivity of the DMN across spatial scales with cell-type resolution. We co-registered maps from functional magnetic resonance imaging and axonal tracing experiments into the 3D Allen mouse brain reference atlas. We find that the mouse DMN consists of preferentially interconnected cortical regions. As a population, DMN layer 2/3 (L2/3) neurons project almost exclusively to other DMN regions, whereas L5 neurons project in and out of the DMN. In the retrosplenial cortex, a core DMN region, we identify two L5 projection types differentiated by in- or out-DMN targets, laminar position, and gene expression. These results provide a multi-scale description of the anatomical correlates of the mouse DMN.