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Transforming representations of movement from body- to world-centric space.
Lu, Jenny; Behbahani, Amir H; Hamburg, Lydia; Westeinde, Elena A; Dawson, Paul M; Lyu, Cheng; Maimon, Gaby; Dickinson, Michael H; Druckmann, Shaul; Wilson, Rachel I.
Afiliação
  • Lu J; Department of Neurobiology and Howard Hughes Medical Institute, Harvard Medical School, Boston, MA, USA.
  • Behbahani AH; Division of Biology and Biological Engineering, California Institute of Technology, Pasadena, CA, USA.
  • Hamburg L; Department of Neurobiology, Stanford University, Stanford, CA, USA.
  • Westeinde EA; Department of Neurobiology and Howard Hughes Medical Institute, Harvard Medical School, Boston, MA, USA.
  • Dawson PM; Department of Neurobiology and Howard Hughes Medical Institute, Harvard Medical School, Boston, MA, USA.
  • Lyu C; Laboratory of Integrative Brain Function and Howard Hughes Medical Institute, The Rockefeller University, New York, NY, USA.
  • Maimon G; Laboratory of Integrative Brain Function and Howard Hughes Medical Institute, The Rockefeller University, New York, NY, USA.
  • Dickinson MH; Division of Biology and Biological Engineering, California Institute of Technology, Pasadena, CA, USA.
  • Druckmann S; Department of Neurobiology, Stanford University, Stanford, CA, USA.
  • Wilson RI; Department of Neurobiology and Howard Hughes Medical Institute, Harvard Medical School, Boston, MA, USA. rachel_wilson@hms.harvard.edu.
Nature ; 601(7891): 98-104, 2022 01.
Article em En | MEDLINE | ID: mdl-34912123
ABSTRACT
When an animal moves through the world, its brain receives a stream of information about the body's translational velocity from motor commands and sensory feedback signals. These incoming signals are referenced to the body, but ultimately, they must be transformed into world-centric coordinates for navigation1,2. Here we show that this computation occurs in the fan-shaped body in the brain of Drosophila melanogaster. We identify two cell types, PFNd and PFNv3-5, that conjunctively encode translational velocity and heading as a fly walks. In these cells, velocity signals are acquired from locomotor brain regions6 and are multiplied with heading signals from the compass system. PFNd neurons prefer forward-ipsilateral movement, whereas PFNv neurons prefer backward-contralateral movement, and perturbing PFNd neurons disrupts idiothetic path integration in walking flies7. Downstream, PFNd and PFNv neurons converge onto hΔB neurons, with a connectivity pattern that pools together heading and translation direction combinations corresponding to the same movement in world-centric space. This network motif effectively performs a rotation of the brain's representation of body-centric translational velocity according to the current heading direction. Consistent with our predictions, we observe that hΔB neurons form a representation of translational velocity in world-centric coordinates. By integrating this representation over time, it should be possible for the brain to form a working memory of the path travelled through the environment8-10.
Assuntos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Percepção Espacial / Encéfalo / Drosophila melanogaster / Navegação Espacial / Memória Espacial / Locomoção / Modelos Neurológicos Tipo de estudo: Prognostic_studies Limite: Animals Idioma: En Revista: Nature Ano de publicação: 2022 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Percepção Espacial / Encéfalo / Drosophila melanogaster / Navegação Espacial / Memória Espacial / Locomoção / Modelos Neurológicos Tipo de estudo: Prognostic_studies Limite: Animals Idioma: En Revista: Nature Ano de publicação: 2022 Tipo de documento: Article